Skip to main content

Identifying potential patient-specific predictors for anterior cruciate ligament reconstruction outcome – a diagnostic in vitro tissue remodeling platform



Upon anterior cruciate ligament (ACL) rupture, reconstruction is often required, with the hamstring tendon autograft as most widely used treatment. Post-operative autograft remodeling enhances graft rupture risk, which occurs in up to 10% of the patient population, increasing up to 30% of patients aged under 20 years. Therefore, this research aimed to identify potential biological predictors for graft rupture, derived from patient-specific tissue remodeling-related cell properties in an in vitro micro-tissue platform.


Hamstring tendon-derived cells were obtained from remnant autograft tissue after ACL reconstructions (36 patients, aged 12–55 years), and seeded in collagen I gels on a micro-tissue platform. Micro-tissue compaction over time – induced by altering the boundary constraints – was monitored. Pro-collagen I expression was assessed using ELISA, and protein expression of tenomodulin and α-smooth muscle actin were measured using Western blot. Expression and activity of matrix metalloproteinase 2 were determined using gelatin zymography.


Only micro-tissues corresponding to younger patients occasionally released themselves from the constraining posts. Pro-collagen I expression was significantly higher in younger patients. Differences in α-smooth muscle actin and tenomodulin expression between patients were found, but these were age-independent. Active matrix metalloproteinase 2 expression was slightly more abundant in younger patients.


The presented micro-tissue platform exposed patient-specific remodeling-related differences between tendon-derived cells, with the micro-tissues that released from constraining posts and pro-collagen I expression best reflecting the clinical age-dependency of graft rupture. These properties can be the starting point in the quest for potential predictors for identifying individual patients at risk for graft rupture.


The anterior cruciate ligament (ACL) connects the femur to the tibia and is one of the most important ligaments for knee joint stability. It consists of a predominately anisotropic collagen I extracellular matrix populated by fibroblast-like cells [24]. Upon acute overloading (trauma), the ACL can rupture, with a prevalence of 100,000–200,000 per year in the United States [9]. A ruptured ACL impairs knee stability, can impede the patient’s normal activity levels, and even lead to work-related disabilities. A completely torn ACL does not self-regenerate, and therefore, in 50% of the rupture cases an ACL reconstruction is required [18], often performed using a hamstring tendon (e.g., semitendinosus/gracilis tendon) autograft [28, 51].

After ACL reconstruction with an autograft, a remodeling process is initiated that transforms the tissue to match its new (mechanical) environment [16]. This remodeling can roughly be divided in an early graft healing phase, a proliferation phase and a ligamentization phase [18, 38, 41]. The early graft healing phase with central graft necrosis, hypocellularity and no detectable revascularization – resulting in nutrient deprivation – occurs in approximately the first 4 weeks after surgery. The necrotic fibroblasts secrete cytokines (e.g., tumor necrosis factor-α, interleukin 6, vascular endothelial growth factor (VEGF)) and matrix metalloproteases (MMPs) [55]. The latter mainly comprise collagenases (MMP1, MMP8 and MMP13) and gelatinases (MMP2 and MMP9), which break down the collagen extracellular matrix gradually [48]. The proliferation phase covers approximately the second and third month after surgery. VEGF-induced graft vascularization supplies cell nutrients, and combined with the cytokines secreted in the early graft healing phase, this stimulates myofibroblasts – characterized by α-smooth muscle actin (αSMA) expression – from the synovial fluid to invade the graft. The myofibroblasts produce more collagen III relative to collagen I, and deposit this more isotropically. In this phase, MMP production is high as well, which combined with the isotropic collagen III seriously impairs graft strength [18, 38, 41]. The ligamentization phase can last up to 2 years after surgery and is characterized by (partial) recovery of the fibroblastic cell phenotype. The cells align with the main loading direction, deposit anisotropic collagen I and therefore graft strength increases towards – but never fully attains – that of the native ACL [17, 18, 38, 41]. It can take up to 2 years after surgery for patients to return to their pre-injury activity level [33], which is ultimately achieved by approximately 65% of recreational athletes [3].

Early return to sports, traumatic re-injury, concomitant knee instabilities, surgical errors and/or impaired graft strength during remodeling – particularly the proliferation phase – can lead to ACL graft rupture, which occurs for up to 10% of the patients, and for patient younger than 20 years this increases even up to 30% [13, 14, 27, 33, 52]. This age-dependency of graft rupture risk could be ascribed to larger participation in (risk-taking) activities by younger patients, but biological differences in the tissue remodeling process may also contribute [27, 52]. Besides age, biological differences in tissue remodeling may also be related to gender [21], and which hamstring tendon is used for the reconstruction: an adequate autograft can usually be made of the semitendinosus tendon, but sometimes the gracilis tendon needs to be added [12, 20], and variations in regenerative capacity between both tendons have been observed [34]. Currently, it remains unknown whether graft rupture risk can be predicted from the biological properties of the resident fibroblasts-like cells in the graft. Therefore, the aims of this research were: 1) to assess various patient-specific tissue remodeling-related properties of human hamstring tendon-derived cells (TDCs; obtained from remnant autograft tissue after ACL reconstructions) in an in vitro micro-tissue remodeling platform; and 2) to relate the remodeling-related properties of patient-derived cells to patient age, gender and tendon type (semitendinosus or gracilis tendon), in order to identify cell properties that could potentially predict graft rupture.


Harvesting and expanding tendon-derived cells

Remnant tissue fragments from the most proximal and/or distal part of semitendinosus and/or gracilis tendons were collected after Institutional Review Board approval (METC N16.148) and processed immediately after ACL reconstructive surgery. The tendon fragments were disinfected with 70% ethanol and washed repeatedly with sterile phosphate buffered saline (PBS). The tissue was cut into small pieces and the extracellular matrix was dissolved in a sterile-filtered 2 mg/ml collagenase IV (Gibco, 17,104,019) solution in Dulbecco’s PBS (DPBS; Sigma-Aldrich, D4031) at 37 °C. After 6–22 h (depending on the tissue volume as well as time of day of surgery), the solution was centrifuged for 5 min at 1100 rpm, and the supernatant was discarded. The pellet containing cells and small tissue fragments was resuspended in medium consisting of high-glucose Dulbecco’s Modified Eagle Medium (HG-DMEM; Gibco, 42,430–025) and Nutrient Mixture F-12 Ham (F12; Gibco, 21,765–029) in a 1:1 (v/v) ratio, supplemented with 20% fetal bovine serum (FBS; Sigma-Aldrich, F7524) and 5% penicillin-streptomycin (pen-strep; Lonza, DE17-602E), and cultured for 7 days at 37 °C and 5% CO2 with 2–3 medium changes. Subsequently, the pen-strep concentration was lowered to 1%, and TDCs were cultured until cryopreservation after reaching sub-confluency in passage 1 or 2. In total, TDCs were successfully harvested from 41 tendons obtained from 36 patients (Table 1; Table S-1 for a complete overview).

Table 1 Demographics and origin of tissue fragments

Micro-tissue culture, compaction and image processing

After cryopreservation, TDCs were grown to sub-confluency in growth medium consisting of HG-DMEM and F12 (1:1) with 10% FBS and 1% pen-strep and seeded in a micro-tissue platform as described before [7]. Briefly, systems of Dragon Skin™ (Smooth On, Dragon Skin™ 10 SLOW) posts were cast in 6-well plates (Fig. 1), disinfected with 70% ethanol, and treated with 0.2% Pluronic® F-127 (Sigma-Aldrich, P2443) in MilliQ for 1 h, to make surfaces non-adhesive. Afterwards, systems were washed with sterile MilliQ and UV-sterilized. TDCs were suspended at 1.5 million cells/ml in 71% (v/v) growth medium, 25% rat tail collagen I (Advanced Biomatrix, 5056) and 4% 1 M NaOH (Merck, 106,498) in PBS. 60 μl cell suspension was seeded in each system (Fig. 1), and after 45 min gelation at 37 °C, 4 ml growth medium, supplemented with 0.25 mg/ml L-ascorbic acid-2-phosphate sesquimagnesium (Sigma-Aldrich, A8960), was added to each well.

Fig. 1
figure 1

Schematic overview of the experimental procedure in the micro-tissue platform. To the array of micro posts (grey), a suspension of cells and collagen (pink) was added. Cells contracting and applying force to their collagenous environment results in formation of a predominantly isotropic micro-tissue around the constraining posts in the subsequent 48 h. By releasing the tissue constraints of the four outermost posts, a tissue remodeling process is initiated that results in further compaction into a more anisotropic tissue during the next 48 h

After 48 h, micro-tissues had formed around the posts due to collagen gel compaction by the TDCs. The constraints of the four outermost post were released, inducing further micro-tissue compaction (Fig. 1), which was monitored using brightfield imaging in a Leica DMi8 microscope with incubation box at 37 °C and 5% CO2. An image was made every hour, for 48 h. Micro-tissues in additional well plates that could not be monitored simultaneously were imaged immediately after releasing the constraints and 48 h later using an EVOS™ XL Core microscope (ThermoFischer Scientific). Micro-tissues that were still constrained by the remaining posts after 48 h were snap-frozen and stored at − 80 °C until further use in the follow-up analyses described below. Micro-tissues that had released from the remaining posts were not processed for further analyses. For a few patients, the number of micro-tissues was too low to perform all follow-up analyses or repeat an unsuccessful read-out. The number of patients included in each analysis is presented in Figs. 3, 4, 5 and 6.

Microscopy images were analyzed using a custom-made Matlab (MathWorks) script calculating the top-view surface area of the micro-tissues over time, based on a grey value threshold, which is illustrated in Fig. 2 strategy A. For images where the absolute intensity values were insufficient to identify the micro-tissue silhouette, edge detection was performed on the original images in ImageJ [42] before applying the Matlab script (Fig. 2 strategy B).

Fig. 2
figure 2

Steps to obtain top-view micro-tissue surface area. (A) Based on absolute intensity values: the original image (A1) was binarized (A2), the largest connected component was selected, and any remaining holes were filled (A3). The object size (in pixels) was counted and converted to the absolute surface area. In case strategy A failed, strategy B was applied. (B) Based on micro-tissue: on the original image (B1) edge detection was performed (B2). Image 2 was binarized (B3), and subtracted from the original image (B4). The resulting image was binarized (B5), the largest connected component was selected, and any remaining holes were filled (B6)

Pro-collagen I ELISA

Collagen I production was assessed with ELISA, by means of human pro-collagen I expression. One snap-frozen micro-tissue per remnant hamstring tendon tissue was lysed in 100 μl RIPA buffer (Sigma-Aldrich, R0278) on ice, and sonicated. Pro-collagen I expression was assessed using the Human Pro-Collagen I alpha 1 Matched Antibody Pair Kit (Abcam, ab216064), according to the manufacturer’s instructions, and quantified using the included pro-collagen I alpha 1 standard.

As a sample loading control, samples were semi-quantitatively tested for similarity of cell lysate contents using Western blot for housekeeping protein tubulin (following the method in the section ‘Western blot’), and outliers were defined as more than 1.5x the inter-quartile range below the first quantile or above the third quantile [19].

Western blot

For protein expression analysis of tendon marker tenomodulin (37 kDa), myofibroblast marker αSMA (42 kDa) and housekeeping protein tubulin (50–55 kDa), one snap-frozen micro-tissue per hamstring tendon tissue was lysed as described above. Lysed samples were mixed 1:1 (v/v) with Laemmli buffer (composition in Supplementary material) and 20% (v/v) 100 mM 1,4-dithiothreitol (Sigma-Aldrich, D0632) in MilliQ, and denatured for 5 min at 98 °C. Samples were loaded in 10% polyacrylamide gels (Biorad, 1,610,158) (composition in Supplementary material) and separated by size using gel electrophoresis at 15 mA per gel for approximately 1.5 h.

Afterwards, proteins were transferred overnight to a blotting membrane, at 4 °C and 25 V. The membrane was blocked for 30 min with 50 mg/ml milk (Campina, Elk skimmed milk powder) in PBS/0.1% Tween (Sigma-Aldrich, 8.22184), followed by overnight incubation at 4 °C of the primary antibodies: rabbit anti-tenomodulin (Abcam, ab203676; 1:4000), rabbit anti-αSMA (Abcam, ab5694; 1:2000) and rat anti-tubulin (Novus Biologicals, NB600–506; 1:4000) in 50 mg/ml milk in PBS/0.1% Tween. The blot was incubated with the secondary antibodies: goat anti-rabbit HRP (Abcam, ab6721; 1:20,000) followed by rabbit anti-rat (Invitrogen, 61–9520; 1:20,000) in 5 mg/ml milk in PBS/Tween for 1 hour each. Finally, the blot was incubated for 2 min with Super SignalWest Dura Extended Duration Substrate (Thermofisher, 34,075), and visualized with the Isogen ProXima. Protein band intensities on the Western blots were determined using a custom-made script in Matlab.

Gelatin zymography

For measuring MMP2 expression and activity using zymography, one snap-frozen micro-tissue per hamstring tendon tissue was lysed as for ELISA, and centrifuged for 10 min at 2000 rpm at 4 °C. The supernatant was mixed 2:1 (v/v) with sample buffer (composition in Supplementary material), loaded in 10% polyacrylamide/10% gelatin gels (composition in Supplementary material), and separated using gel electrophoresis at 120 V for approximately 1.5 h. The gel was permeabilized using 2.5% Triton X-100 (Millipore, 1.08603) in MilliQ for 2 × 30 min, and rinsed overnight in substrate buffer (composition in Supplementary material), both at 37 °C. Afterwards, the gel was stained for 2 h at room temperature while gently shaking, followed by 2 × 30 min de-staining (composition of both solutions in Supplementary material). Gels were visualized with the Isogen ProXima. Active MMP2 (62 kDa) and inactive MMP2 (pro-MMP2; 72 kDa) band intensities were determined as for Western blot and normalized to global (image) background and local (gel) background intensity. The active fraction was expressed as the active MMP2 protein band intensity divided by the total amount, e.g. active and inactive MMP2 band intensities combined. Gelatin zymography is also suitable to visualize MMP9 (92 kDa) protein bands, but these were not visible in our experiments.

Statistical analysis

Statistical analyses were performed using R Commander [8]. For all read-outs normality was assessed with quantile-comparison plots. Multiple Regression Models were tested with age, gender and tendon type as independent variables and relative micro-tissue surface area after 48 h, pro-collagen I, tenomodulin, αSMA or active MMP2 protein expression or MMP2 active fraction as dependent variables. Similarly, for intact/released micro-tissues as dependent variable, a Logistic Generalized Linear Model was tested with age, gender and tendon type as independent variables. In all analyses, the significance level was set at α = 0.05.


Micro-tissues corresponding to younger patients compact faster and release from posts more often compared to older patients

Micro-tissues were produced with cells from 41 tendons obtained from 36 patients. For 2 tendons (#7: ♀ 27y semitendinosus; #24: ♂ 19y semitendinosus) these micro-tissues released from the posts already before the constraints of the outermost posts were released. For both patients, cells from the gracilis were not available, and therefore these patients could not be included in further analysis. Top-view micro-tissue surface areas corresponding to the remaining 39 tendons are shown in Figure S-1, and the surface area after 48 h relative to 0 h is depicted in Fig. 3a. This relative surface area was significantly dependent on age (p = 0.012), but not on gender (p = 0.13) or tendon (p = 0.23) (Table 2).

Fig. 3
figure 3

Micro-tissues representative for younger patients occasionally released from the posts during induced remodeling. a Top-view surface area after 48 h remodeling relative to 0 h, and b micro-tissues staying intact or releasing from remaining posts compared to patient age. Significant age-dependencies were detected for both the relative surface areas and micro-tissues staying intact versus those that released. n = 41

Table 2 Results multiple regression models. a Pseudo-R2, since multiple R2 is not defined for logistic regression

As can be observed in Fig. 3a and is indicated by the crosses (×) in Figure S-1, micro-tissues corresponding to 10 tendons from 9 patients released from the posts during the induced compaction, and the oldest patient this happened for was 27 years (Fig. 3b). Micro-tissues corresponding to the remaining 31 tendons from 27 patients remained intact over 48 h and were included in further analyses – as well as one single intact micro-tissue from patient #28. Whether micro-tissues were intact or released from the posts was significantly age-dependent (p = 0.042), but independent of gender (p = 0.10) or tendon type (p = 0.07) (Table 2).

Pro-collagen I expression decreases with patient age

To determine patient-specific production of collagen I by the TDCs, human pro-collagen I protein expression in the lysed micro-tissues was quantified using ELISA (Fig. 4). Semi-quantified cell lysate contents – by means of protein band intensities in Western blots for housekeeping protein tubulin – are shown in Figure S-2C. Identified outliers (Figure S-2D) are in Fig. 4 indicated by the open symbols. There were only outliers with a tubulin protein band intensity below average.

Fig. 4
figure 4

Pro-collagen I content decreased with increasing patient age, with an apparent patient cut-off age around 25 years. Patient-specific human pro-collagen I α1 content per micro-tissue was measured using ELISA and analyzed with respect to patient age. Outliers in cell lysate content are indicated by the open symbols . n = 28

Pro-collagen I content was up to 5 times higher for younger patients and dropped for older patients with an apparent threshold around 25 years. The age-dependency of pro-collagen amount was statistically significant (p = 0.01), opposed to gender (p = 0.32) or tendon type (p = 0.51) (Table 2).

Inter-patient variations in αSMA and tenomodulin protein expression are independent of age

In order to investigate phenotypic properties of the TDCs in the micro-tissues, protein expression of tenogenic marker tenomodulin and myofibroblast marker αSMA were semi-quantitatively determined using Western blot. Western blot bands can be found in Figure S-2, and protein band intensities normalized to housekeeping protein tubulin are shown in Fig. 5.

Fig. 5
figure 5

Large inter-patient differences in tenomodulin and αSMA expression were observed, although there was no significant age-dependency. Semi-quantitative protein expression of (a) tenomodulin and (b) myofibroblast marker α-smooth muscle actin (αSMA) were measured using Western Blot, and compared to patient age. n = 32

Protein expression of tenomodulin (Fig. 5a) was remarkably low, with visible protein bands in only 2 samples, although an intensity signal was detected in the image analysis of all samples. Expression of αSMA (Fig. 5b) displayed up to 21-fold differences between patients. Interestingly, higher expression of stress fiber protein αSMA did not seem to be associated with faster or stronger compaction of the micro-tissues. No significant dependencies on age (tenomodulin: p = 0.64; αSMA: p = 0.50), gender (p = 0.61; p = 0.24) or tendon type (p = 0.71; p = 0.24) were observed for either of the proteins (Table 2).

Active MMP2 is slightly more abundant in younger patients, whereas MMP2 active fraction shows little inter-patient variation

As a measure for matrix-degrading enzyme activity, MMP2 activity was determined using gelatinase zymography. MMP9 (92 kDa) protein bands were not visible. Zymograph bands of active MMP2 (62 kDa) and inactive MMP2 (pro-MMP2; 72 kDa) are depicted in Figure S-3, and resulting calculated active MMP2 intensities and active fractions are shown in Fig. 6a and b, respectively. Active MMP2 intensity was independent of gender (p = 0.65) or tendon type (p = 0.95), and appeared slightly higher in younger patients, but this trend was non-significant (p = 0.48). Only minor inter-patient differences in active fractions were observed, and significant dependencies on age (p = 0.64), gender (p = 0.98) or tendon type (p = 0.12) were absent (Table 2).

Fig. 6
figure 6

Active MMP2 was (non-significantly) more abundant in younger patients, whereas the active fraction MMP2 varied only little between patients. a Protein band intensities for active MMP2 on gelatinase zymography. b MMP2 active fraction, defined as the protein band intensity for active MMP2 divided by the total amount, e.g. active and inactive MMP2 protein band intensities combined. Both quantities were compared to patient age. n = 30


Reconstructive surgery upon ACL rupture – predominantly performed using the hamstring autograft – results in graft rupture in up to 10% of the patient population, increasing up to 30% of patients aged under 20 years. Inter-patient differences in tissue remodeling capacity, which are possibly age-related, can affect graft remodeling after surgery and therefore graft rupture risk. This creates opportunities for predicting patient-specific risk of graft rupture, but suitable predictors have not been identified yet. Therefore, the aims of this research were to assess patient-specific remodeling-related properties of patient TDCs from remnant tissue after ACL reconstructions with a hamstring tendon autograft, in an in vitro micro-tissue platform, and to identify potential patient-specific in vitro predictors for ACL graft rupture from these properties. For this purpose, tissue remodeling-related cellular properties of human hamstring TDCs were related to patient age, gender and type of hamstring tendon. TDCs were harvested from remnant tissue after ACL reconstructive surgeries and seeded in collagen I gels to form micro-tissues. After releasing micro-post constraints, the micro-tissues showed greater tissue compaction and even released from the remaining posts for some of the younger (≤27 years) patients. For the intact tissues, pro-collagen I, tenomodulin and αSMA expression, and MMP2 activity were determined. Pro-collagen I expression was significantly higher in cells from younger patients, with an apparent threshold around 25 years. Tenomodulin and αSMA expression varied between patients but were age-independent. Active MMP2 seemed slightly more abundant in younger patients, but MMP2 active fraction was almost equal for all patients. None of the read-outs was dependent on gender or tendon type.

Previous studies revealed intra-patient differences between the native ACL and hamstring tendon autograft before implantation, that converged after graft implantation [10, 23, 30, 46]. However, in order to identify potential predictors or risk factors for graft rupture, inter-patient variations of tissue properties need to be determined. To our knowledge, this is the first study comparing cellular properties of hamstring tendon autograft tissue from a large group of patients undergoing an ACL reconstruction, and relating this to patient age, which revealed potential predictors for graft rupture. A similar research was conducted for the outcome of rotator cuff repair [37], where cell growth and collagen production were age-dependent, whereas gender had no effect. However, no correlation between cell properties and clinical outcome of the rotator cuff repair was detected.

Releasing post constraints from the in vitro system induced micro-tissue remodeling and compaction via an altered equilibrium of cellular contraction and extracellular matrix stiffness [39]. The fact that some micro-tissues released from the remaining posts indicates that those cells were more contractile, and remarkably, this only occurred for cells from younger (≤27 years) patients. Reduced tendon (cell) contractility with age has been described before in rodents [25, 26], and was mostly ascribed to higher numbers of (αSMA-expressing) myofibroblasts in the tissue [53], but αSMA expression was not associated with faster or more compaction in the present study. Increased cell contractility in vivo would intuitively increase graft tension. Higher initial graft tension provides better patient outcomes – although too high tension can over-constrain the joint [6]. However, a link between tension and graft rupture risk has not been described. Still, cell contractility in vitro might have predictive value for in vivo outcome.

Pro-collagen I expression by the TDCs in the micro-tissues – as a measure for collagen production – was significantly age-dependent, decreasing up to 5-fold for patients older than 25 years. Literature on this subject is inconclusive, reporting both increasing and decreasing collagen content or production with age, as well as absence of age-dependency, in tendons and other tissues [22, 29, 36, 47, 50]. Nevertheless, the age-related pro-collagen I expression in this research did reflect the age-dependency of graft rupture rates as reported in literature [52], but it seems counterintuitive that graft rupture risk may increase with higher collagen production. We speculate though, that higher collagen production can induce fibrosis formation, when synthesis exceeds degradation [54]. This seems plausible to occur in certain younger patients, considering an expected average balance between collagen synthesis and degradation in healthy remodeling [1], as well as the reported non-significant age-dependency of active MMP2 expression and almost constant MMP2 active fraction. Besides that, faster collagen turn-over might be at the expense of collagen organization and therefore reduce mechanical strength [35].

The phenotypic properties of the TDCs in the micro-tissues were determined by means of tenomodulin and αSMA protein expression. However, neither of the protein expression levels was dependent on age, gender or tendon type. Particularly the independency of age, in contrast to the age-dependency of in vivo graft rupture described in literature, probably excludes these protein expression levels as in vitro predictor for in vivo graft rupture risk. It should be noted here that non-physiological in vitro culture conditions (i.e. high serum levels, hypercellularity and random cell morphology) can induce phenotypic drift of TDCs away from the tenogenic lineage [1, 49].

Statistically non-significant variations in active MMP2 protein band intensities following a decreasing trend with patient age were observed, implying inter-patient differences in protein expression. However, MMP2 active fraction was found almost equal in all patients. In previous research, increasing MMP2 expression [15, 56] and activity [31] with age were described in tendon and non-tendon tissues. Those samples were however directly obtained from human tissue (including inter-patient variation), whereas the homologous extracellular environment in our micro-tissues and presence of MMP2 in serum [4] may have evened out these parameters.

Whether the independent biological factors patient age, gender and tendon type (semitendinosus vs. gracilis) from this research are risk factors for in vivo graft rupture has been investigated before. Lower age is a well-known risk factor, and whereas the threshold is mostly set at 20 years [27, 52], intermediate re-rupture rates between 18 and 25 years have also been reported [43]. This matches the age-dependency we observed in pro-collagen I expression and micro-tissue release, with apparent thresholds around 25 and 27 years, respectively. Although female subjects are at higher risk of ACL rupture [45], this gender-dependency is not observed in graft rupture risk [40, 43], supporting our data where no gender-dependencies were detected in the biological properties of the TDCs from remnant autograft tissue. It has been reported before that use of a semitendinosus tendon alone or combined with a gracilis tendon as autograft does not affect in vivo graft rupture risk [40], in parallel to the absence of a significant difference between the tendon types in this study. The fact that remnant tissue from both the semitendinosus and the gracilis tendon was available for some patients, enabled intra-patient comparison of the cellular biological properties. Whether micro-tissues released from the posts or stayed intact was always equal for both tendons of the same patient. This underlined the patient-specificity of this read-out – independent of whether the semitendinosus tendon alone is used for the autograft or combined with the gracilis tendon – and consequently its potential as predictor for clinical outcome. For the other parameters, however, intra-patient variations were similar to inter-patient variations. This implies measurement variations originate from tissue-specific rather than patient-specific cell properties.

A few limitations and side notes of the current study need to be considered. Biological properties of the resident cells of ACL autografts were examined in this research, however, many of these cells are lost in the early graft healing phase of remodeling, and the graft properties are affected by the invading cells afterwards [32]. Therefore, it may be useful for future research to also investigate biological, remodeling-related properties of synovial fluid-derived cells and possibly identify predictors for graft rupture. Similarly, it should be noted that the high protein expression of αSMA in our system can be ascribed to trans-differentiation of the TDCs, whereas this in vivo mostly originates from invading myofibroblasts [32]. Before the cell isolation procedure, the risk for infection was reduced by briefly submerging the tissue in an ethanol solution. This treatment may have affected cell viability, but we believe this was limited to the tissue surface, since the time span for ethanol penetration into tendon tissue is in the range of hours [2]. The cell isolation procedure itself might have affected TDC properties too, but this approach was chosen since it enabled a wider screening of remodeling-related cell properties and fair comparison of the read-outs for all patients in a controlled manner. However, the micro-tissues that released from the posts were excluded from subsequent read-outs, because the time span without micro-post constraints – and therefore an altered mechanical environment for the cells – varied largely between patients, and ranged from 2 h to 37 h. This is in the same order of magnitude or exceeding the production rates of αSMA (approximately 2 h [44]), collagen I and MMP2 (both approximately 2–4 h [5, 11]). Therefore, the cells could have adjusted synthesis of these proteins to the new mechanical environment before the experiment was terminated, and the corresponding read-outs could be dominated by the unconstrained situation, potentially leading to an unfair comparison with the constrained micro-tissues. In follow-up research, the loss of micro-tissues for subsequent read-outs due to release from the constraining posts might be circumvented by including TDCs cultured only in a two-dimensional environment, but also techniques able to measure the identified potential predictors of re-rupture directly in the remnant patient tissue should be considered. That would eliminate successful TDC isolation from the patient inclusion criteria, prevent released micro-tissues to be excluded from subsequent read-outs, and therefore allow for a larger total number of patients included.

Altogether the complex process of in vivo graft remodeling cannot be completely mimicked in vitro in the proposed model system. However, the main criterium for a read-out with predictive value is a strong correlation of TDC properties with patient outcome – rather than mimicking the remodeling process. Despite the fact that more patients were included than in previous comparable studies [23, 37], re-rupture rates of up to 30% for younger patients and up to 10% for older patients which were reported in literature, translate into only a few possible clinical re-rupture cases that can be compared to our in vitro findings. Consequently, there might be insufficient statistical power to correlate in vitro read-outs to graft rupture. Therefore, correlations with other clinical outcomes such as knee stability examination by the orthopedic surgeon and patient reported outcome measures should be included.


In conclusion, remodeling-related biological differences between patient TDCs could be assessed with the in vitro micro-tissue platform, and micro-tissues releasing from the posts and pro-collagen I expression reflected the age-dependency of re-rupture rates – as described in literature – best. Therefore, these read-outs can be the starting point in the quest for potential predictors for identifying individual patients at risk for graft rupture.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.



Anterior cruciate ligament


α-smooth muscle actin


Dulbecco’s phosphate buffered saline


Enzyme-linked immunosorbent assay


Nutrient Mixture F-12 Ham


Fetal bovine serum


High-glucose Dulbecco’s Modified Eagle Medium


Matrix metalloproteinase


Phosphate buffered saline




Tendon-derived cell


Vascular endothelial growth factor


  1. Ackermann PW, Renström P (2012) Tendinopathy in sport. Sports Health 4:193–201

    PubMed  PubMed Central  Google Scholar 

  2. Anastasescou M, Cornu O, Banse X, König J, Hassoun A, Delloye C (1998) Ethanol treatment of tendon allografts: a potential HIV inactivating procedure. Int Orthop 22:252–254

    CAS  PubMed  PubMed Central  Google Scholar 

  3. Ardern CL, Webster KE, Taylor NF, Feller JA (2011) Return to sport following anterior cruciate ligament reconstruction surgery: a systematic review and meta-analysis of the state of play. Brit J Sport Med 45:596–606

    Google Scholar 

  4. Avolio C, Ruggieri M, Giuliani F, Liuzzi GM, Leante R, Riccio P, Livrea P, Trojano M (2003) Serum MMP-2 and MMP-9 are elevated in different multiple sclerosis subtypes. J Neuroimmunol 136:46–53

    CAS  PubMed  Google Scholar 

  5. Campa JS, McAnulty RJ, Laurent GJ (1990) Application of high-pressure liquid chromatography to studies of collagen production by isolated cells in culture. Anal Biochem 186:257–263

    CAS  PubMed  Google Scholar 

  6. DeFroda SF, Karamchedu NP, Budacki R, Wiley T, Fadale PD, Hulstyn MJ, Shalvoy RM, Badger GJ, Fleming BC, Owens BD (2020) Evaluation of graft tensioning effects in anterior cruciate ligament reconstruction between hamstring and bone–patellar tendon bone autografts. J Knee Surg.

  7. Foolen J, Wunderli SL, Loerakker S, Snedeker JG (2018) Tissue alignment enhances remodeling potential of tendon-derived cells-lessons from a novel microtissue model of tendon scarring. Matrix Biol 65:14–29

    CAS  PubMed  Google Scholar 

  8. Fox J (2005) The R commander: a basic-statistics graphical user interface to R. J Stat Softw 14:1–42

    Google Scholar 

  9. Friedberg RP (2019) Anterior cruciate ligament injury. In: Fields KB, Grayzel J (eds) UpToDate Available via Accessed 24 Oct 2019

    Google Scholar 

  10. Ghebes CA, Kelder C, Schot T, Renard AJ, Pakvis DF, Fernandes H, Saris DB (2017) Anterior cruciate ligament-and hamstring tendon-derived cells: in vitro differential properties of cells involved in ACL reconstruction. J Tissue Eng Regen M 11:1077–1088

    CAS  Google Scholar 

  11. Goldman S, Lovett DH, Shalev E (2009) Mechanisms of matrix metalloproteinase-2 (mmp-2) transcriptional repression by progesterone in jar choriocarcinoma cells. Reprod Biol Endocrinol 7.

  12. Goradia VK, Rochat MC, Kida M, Grana WA (2000) Natural history of a hamstring tendon autograft used for anterior cruciate ligament reconstruction in a sheep model. Am J Sports Med 28:40–46

    CAS  PubMed  Google Scholar 

  13. Grindem H, Snyder-Mackler L, Moksnes H, Engebretsen L, Risberg MA (2016) Simple decision rules can reduce reinjury risk by 84% after ACL reconstruction: the Delaware-Oslo ACL cohort study. Brit J Sport Med 50:804–808

    Google Scholar 

  14. Grindem H, Engebretsen L, Axe M, Snyder-Mackler L, Risberg MA (2020) Activity and functional readiness, not age, are the critical factors for second anterior cruciate ligament injury—the Delaware-Oslo ACL cohort study. Brit J Sport Med.

  15. Guo L, Hussain AA, Limb GA, Marshall J (1999) Age-dependent variation in metalloproteinase activity of isolated human Bruch’s membrane and choroid. Invest Ophth Vis Sci 40:2676–2682

    CAS  Google Scholar 

  16. Janssen RPA, Van der Wijk J, Fiedler A, Schmidt T, Sala HA, Scheffler SU (2011) Remodelling of human hamstring autografts after anterior cruciate ligament reconstruction. Knee Surg Sport Tr A 19:1299–1306

    Google Scholar 

  17. Janssen RPA, Scheffler SU (2014) Intra-articular remodelling of hamstring tendon grafts after anterior cruciate ligament reconstruction. Knee Surg Sport Tr A 22:2102–2108

    Google Scholar 

  18. Janssen RPA, Scheffler SU (2018) Graft Remodeling & Ligamentization after ACL reconstruction. In: Prodromos CC (ed) The anterior cruciate ligament: reconstruction and basic science. Saunders, an Imprint of Elsevier, Inc, Philadelphia, pp 342–347

    Google Scholar 

  19. Kabacoff RI (2015) R in action – data analysis and graphics with R. Manning, Shelter Island

    Google Scholar 

  20. Kern M, Love D, Cotter EJ, Postma W (2016) Quadruple-bundle semitendinosus-gracilis graft technique for all-inside anterior cruciate ligament reconstruction. Arthrosc Tech 5:e1317–e1320

    PubMed  PubMed Central  Google Scholar 

  21. Komosinska-Vassev K, Olczyk P, Winsz-Szczotka K, Kuznik-Trocha K, Klimek K, Olczyk K (2011) Age-and gender-dependent changes in connective tissue remodeling: physiological differences in circulating MMP-3, MMP-10, TIMP-1 and TIMP-2 level. Gerontology 57:44–52

    CAS  PubMed  Google Scholar 

  22. Koshihara Y, Honda Y (1994) Age-related increase in collagen production in cultured human osteoblast-like periosteal cells. Mech Ageing Dev 74:89–101

    CAS  PubMed  Google Scholar 

  23. Lane JG, McFadden P, Bowden K, Amiel D (1993) The ligamentization process: a 4 year case study following ACL reconstruction with a semitendinosis graft. Arthroscopy 9:149–153

    CAS  PubMed  Google Scholar 

  24. Laurencin CT, Freeman JW (2005) Ligament tissue engineering: an evolutionary materials science approach. Biomaterials 26:7530–7536

    CAS  PubMed  Google Scholar 

  25. Lavagnino M, Gardner K, Arnoczky SP (2013) Age-related changes in the cellular, mechanical, and contractile properties of rat tail tendons. Connect Tissue Res 54:70–75

    PubMed  Google Scholar 

  26. Lavagnino M, Bedi A, Walsh CP, Sibilsky Enselman ER, Sheibani-Rad S, Arnoczky SP (2014) Tendon contraction after cyclic elongation is an age-dependent phenomenon: in vitro and in vivo comparisons. Am J Sports Med 42:1471–1477

    PubMed  Google Scholar 

  27. Löcherbach C, Zayni R, Chambat P, Sonnery-Cottet B (2010) Biologically enhanced ACL reconstruction. Orthop Traumatol-Sur 96:810–815

    Google Scholar 

  28. Mahapatra P, Horriat S, Anand BS (2018) Anterior cruciate ligament repair–past, present and future. J Exp Ortop 5.

  29. Mariotti A, Hassell T, Kaminker P (1993) The influence of age on collagen and non-collagen protein production by human gingival epithelial cells. Arch Oral Biol 38:635–640

    CAS  PubMed  Google Scholar 

  30. Marumo K, Saito M, Yamagishi T, Fujii K (2005) The “ligamentization” process in human anterior cruciate ligament reconstruction with autogenous patellar and hamstring tendons: a biochemical study. Am J Sports Med 33:1166–1173

    PubMed  Google Scholar 

  31. McNulty M, Spiers P, McGovern E, Feely J (2005) Aging is associated with increased matrix metalloproteinase-2 activity in the human aorta. Am J Hypertens 18:504–509

    CAS  PubMed  Google Scholar 

  32. Min BH, Han MS, Woo JI, Park HJ, Park SR (2003) The origin of cells that repopulate patellar tendons used for reconstructing anterior cruciate ligaments in man. J Bone Joint Surg Br 85:753–757

    CAS  PubMed  Google Scholar 

  33. Nagelli CV, Hewett TE (2017) Should return to sport be delayed until 2 years after anterior cruciate ligament reconstruction? Biological and functional considerations. Sports Med 47:221–232

    PubMed  PubMed Central  Google Scholar 

  34. Nikolaou VS, Efstathopoulos N, Wredmark T (2007) Hamstring tendons regeneration after ACL reconstruction: an overview. Knee Surg Sport Tr A 15:153–160

    Google Scholar 

  35. Nimni ME (1983) Collagen: structure, function, and metabolism in normal and fibrotic tissues. Semin Arthritis Rheu.

  36. Parry DAD, Craig AS, Barnes GRG (1978) Tendon and ligament from the horse: an ultrastructural study of collagen fibrils and elastic fibres as a function of age. P Roy Soc Lond B Bio 203:293–303

    CAS  Google Scholar 

  37. Pauly S, Stahnke K, Klatte-Schulz F, Wildemann B, Scheibel M, Greiner S (2015) Do patient age and sex influence tendon cell biology and clinical/radiographic outcomes after rotator cuff repair? Am J Sports Med 43:549–556

    PubMed  Google Scholar 

  38. Pauzenberger L, Syré S, Schurz M (2013) “Ligamentization” in hamstring tendon grafts after anterior cruciate ligament reconstruction: a systematic review of the literature and a glimpse into the future. Arthroscopy 29:1712–1721

    PubMed  Google Scholar 

  39. Ristori T, Notermans TMW, Foolen J, Kurniawan NA, Bouten CVC, Baaijens FPT, Loerakker S (2018) Modelling the combined effects of collagen and cyclic strain on cellular orientation in collagenous tissues. Sci Rep 8.

  40. Salmon L, Russell V, Musgrove T, Pinczewski L, Refshauge K (2005) Incidence and risk factors for graft rupture and contralateral rupture after anterior cruciate ligament reconstruction. Arthroscopy 21:948–957

    PubMed  Google Scholar 

  41. Scheffler SU, Unterhauser FN, Weiler A (2008) Graft remodeling and ligamentization after cruciate ligament reconstruction. Knee Surg Sport Tr A 16:834–842

    CAS  Google Scholar 

  42. Schneider CA, Rasband WS, Eliceiri KW (2012) NIH image to ImageJ: 25 years of image analysis. Nat Methods 9:671–675

    CAS  PubMed  PubMed Central  Google Scholar 

  43. Shelbourne KD, Gray T, Haro M (2009) Incidence of subsequent injury to either knee within 5 years after anterior cruciate ligament reconstruction with patellar tendon autograft. Am J Sports Med 37:246–251

    PubMed  Google Scholar 

  44. Springer ML, Ozawa CR, Blau HM (2002) Transient production of α-smooth muscle actin by skeletal myoblasts during differentiation in culture and following intramuscular implantation. Cell Motil Cytoskel 51:177–186

    CAS  Google Scholar 

  45. Sugimoto D, Myer GD, Micheli LJ, Hewett TE (2015) ABCs of evidence-based anterior cruciate ligament injury prevention strategies in female athletes. Curr Phys Med Rehabil Rep 3:43–49

    PubMed  PubMed Central  Google Scholar 

  46. Suzuki D, Takahashi M, Abe M, Nagano A (2008) Biochemical study of collagen and its crosslinks in the anterior cruciate ligament and the tissues used as a graft for reconstruction of the anterior cruciate ligament. Connect Tissue Res 49:42–47

    CAS  PubMed  Google Scholar 

  47. Tuite DJ, Renström PAFH, O'brien M (1997) The aging tendon. Scand J Med Sci Spor 7:72–77

    CAS  Google Scholar 

  48. Vaalamo M (2000) Matrix Metalloproteinases and their inhibitors in Normal and aberrant wound repair. Helsinki: Dissertation, University of Helsinki

  49. Van Vijven M, Wunderli SL, Ito K, Snedeker JG, Foolen J (2020) Serum deprivation limits loss and promotes recovery of tenogenic phenotype in tendon cell culture systems. J Orthop Res.

  50. Varani J, Dame MK, Rittie L, Fligiel SE, Kang S, Fisher GJ, Voorhees JJ (2006) Decreased collagen production in chronologically aged skin: roles of age-dependent alteration in fibroblast function and defective mechanical stimulation. Am J Pathol 168:1861–1868

    CAS  PubMed  PubMed Central  Google Scholar 

  51. Vavken P, Murray MM (2011) The potential for primary repair of the ACL. Sports Med Arthrosc 19:44–49

    PubMed  PubMed Central  Google Scholar 

  52. Webster KE, Feller JA, Leigh WB, Richmond AK (2014) Younger patients are at increased risk for graft rupture and contralateral injury after anterior cruciate ligament reconstruction. Am J Sports Med 42:641–647

    PubMed  Google Scholar 

  53. Weiss M, Unterhauser FN, Weiler A (2012) Crimp frequency is strongly correlated to myofibroblast density in the human anterior cruciate ligament and its autologous tendon grafts. Knee Surg Sport Tr A 20:889–895

    Google Scholar 

  54. Wynn TA (2008) Cellular and molecular mechanisms of fibrosis. J Pathol 214:199–210

    CAS  PubMed  PubMed Central  Google Scholar 

  55. Xie X, Wu H, Zhao S, Xie G, Huangfu X, Zhao J (2013) The effect of platelet-rich plasma on patterns of gene expression in a dog model of anterior cruciate ligament reconstruction. J Surg Res 180:80–88

    CAS  PubMed  Google Scholar 

  56. Yu TY, Pang JHS, Wu KPH, Chen MJ, Chen CH, Tsai WC (2013) Aging is associated with increased activities of matrix metalloproteinase-2 and-9 in tenocytes. BMC Musculoskelet Disord 14.

Download references


Not applicable.


This research was funded by the Eindhoven University of Technology and Máxima MC Eindhoven, but this research did not receive any specific grant from funding agencies in the public, commercial, or non-profit sectors.

Author information

Authors and Affiliations



MvV and JNK performed the cell isolation, micro-tissue culture, imaging and analysis, Western blot and zymography. BvG, MCvdS and RPAJ provided the remnant hamstring tendon tissues. MvD performed the ELISA. MvV interpreted the in vitro data and wrote the first draft of the manuscript manuscript. JF, KI and RPAJ supervised the project. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Marc van Vijven.

Ethics declarations

Ethics approval and consent to participate

The Medical Ethical Committee Máxima MC declared that the rules laid down in Medical Research Involving Human Subjects Acts (WMO) do not apply to this project. The institutional review board approved the execution of this project (N16.148).

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Additional file 1: Figure S1.

Top-view surface areas over time. Top-view surface areas over time of all micro-tissues. Micro-tissues releasing from the posts are indicated with a cross (×).

Additional file 2: Figure S2.

Western blot protein bands. (A) Protein bands in Western blot for αSMA and tubulin (housekeeping protein). (B) Protein bands in Western blot for tenomodulin and tubulin (housekeeping protein). (C) Protein bands in Western blot for tubulin to check cell lysate content of ELISA-samples. (D) Boxplot of semi-quantified tubulin protein band intensities, with identified outliers.

Additional file 3: Figure S3.

Zymograph bands. Protein bands in gelatinase zymography for active MMP2 and inactive (pro-)MMP2.

Additional file 4: Table S1.

Patient data.

Additional file 5.


Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

van Vijven, M., van Groningen, B., Kimenai, J.N. et al. Identifying potential patient-specific predictors for anterior cruciate ligament reconstruction outcome – a diagnostic in vitro tissue remodeling platform. J EXP ORTOP 7, 48 (2020).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI:


  • Anterior cruciate ligament
  • Hamstring tendon autograft
  • In vitro micro-tissue platform
  • Patient-specific cell properties
  • Tissue remodeling