Enhanced Dupuytren's disease fibroblast populated collagen lattice contraction is independent of endogenous active TGF-β2
© Tse et al. 2004
Received: 20 April 2004
Accepted: 12 November 2004
Published: 12 November 2004
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© Tse et al. 2004
Received: 20 April 2004
Accepted: 12 November 2004
Published: 12 November 2004
Dupuytren's disease (DD) is a debilitating fibro-proliferative disorder of the hand characterized by the appearance of fibrotic lesions (nodules and cords) leading to flexion contractures of the fingers and loss of hand function. Although the molecular mechanism of DD is unknown, it has been suggested that transforming growth factor-β2 (TGF-β2) may play an important role in the underlying patho-physiology of the disease. The purpose of this study was to further explore this hypothesis by examining the effects of TGF-β2 on primary cell cultures derived from patient-matched disease and normal palmar fascia tissue using a three-dimensional collagen contraction assay.
Fibroblast-populated collagen lattice (FPCL) contraction assays using primary cell cultures derived from diseased and control fascia of the same DD patients were studied in response to exogenous TGF-β2 and neutralizing anti-TGF-β2 antibodies.
Contraction of the FPCLs occurred significantly faster and to a greater extent in disease cells compared to control cells. The addition of TGF-β2 enhanced the rate and degree of collagen contraction in a dose-dependent fashion for both control and diseased cells. Neutralizing anti-TGF-β2 antibodies abolished exogenous TGF-β2 stimulated collagen contraction, but did not inhibit the enhanced basal collagen contraction activity of disease FPCL cultures.
Although exogenous TGF-β2 stimulated both disease and control FPCL contraction, neutralizing anti-TGF-β2 antibodies did not affect the elevated basal collagen contraction activity of disease FPCLs, suggesting that the differences in the collagen contraction activity of control and disease FPCL cultures are not due to differences in the levels of endogenous TGF-β2 activity.
Dupuytren's disease (DD) is a fibro-proliferative disorder of the palmar fascia (PF) characterized by the formation of fibrous nodules and cords . The disease results in digital contractures, leading to loss of hand function. Surgical excision of the diseased PF is currently the principal form of management since the lack of a clear etiology has precluded the development of other effective and rational forms of treatment.
Since Baron Guillaume Dupuytren's classical description of the disease in 1831, multiple clinical associations have been described, however, no clear molecular mechanism for the disease has been established . Histochemical studies of DD have demonstrated the presence of myofibroblasts , increased production of type III collagen [4–7], and alterations in other extra-cellular matrix proteins including various fibronectin isoforms [8–14]. These biological features are characteristic of abnormal growth factor regulation, specifically fibrogenic cytokines such as transforming growth factor-beta (TGF-β). Several studies have documented TGF-β expression in DD palmar fascia using RT-PCR , in-situ hybridization , and immunohistochemistry [16–18], while others have shown that TGF-β can stimulate cell proliferation [18–20] and promote myofibroblast differentiation in vitro . As a result of these and other studies it has been suggested that an aberrant TGF-β activity may be involved in the pathogenesis of DD.
In this study, we chose to focus on TGF-β2 and its effects on collagen contraction in vitro using a three-dimensional fibroblast populated collagen lattice (FPCL) contraction assay and DD patient-matched disease and control primary cell cultures. Previous reports have examined the role of TGF-β in DD by comparing disease fibroblasts to 'control' fibroblasts obtained from transverse carpal ligament material obtained from patients undergoing carpal tunnel release (CTR). By contrast, the control fibroblast cultures used in this study were established from unaffected PF tissue from the same patient, thus providing us with unique patient- and tissue- matched control cultures. The observed phenotypic differences between patient/tissue-matched control and disease FPCL cultures, specifically elevated collagen contraction activity, and β-catenin and fibronectin (Fn) expression in disease cells [22–24], raises the intriguing possibility that pro-fibrotic factors, such as TGF-β2, may be regulating these disease-associated events in vitro, since TGF-βs are known to promote fibroblast mediated collagen contraction [21, 25, 26] and up-regulate collagen, Fn and β-catenin [20, 27–30]. As described in detail below, we have found that exogenous TGF-β2 could significantly stimulate 'normal' and disease FPCL contraction in a dose-dependent manner. While neutralizing anti-TGF-β2 antibodies completely blocked exogenous TGF-β2 stimulated FPCL contraction they had no effect on the enhanced basal collagen contraction activity of disease FPCL cultures.
Our study protocol was cleared through the UWO Ethics Committee for Research Involving Human Subjects. Areas of diseased fascia and uninvolved normal (control) PF tissue were collected during surgery. DD explant cultures were initially cultured in starter media consisting of α-MEM (Gibco, Invitrogen Corporation) supplemented with 20% fetal bovine serum (FBS, Clontech Laboratories, Palo Alto, CA), and antibiotics (Penicillin G and streptomycin sulfate) and fungizone (Gibco, Invitrogen Corporation) as previously described . Established primary culture lines were maintained in α-MEM + 10% FBS + antibiotics + fungizone. Culture flasks were incubated at 37°C in a humidified chamber with 5% CO2. Medium was changed every 4–5 days and the cells sub-cultured using 0.05% Trypsin-EDTA (Gibco, Invitrogen Corporation, Grand Island, NY) when confluent.
Collagen contraction was carried out using patient-matched disease (D) and control (C) primary cultures (passages 2 – 6) established from patient-matched DD lesions and uninvolved palmar fascia (control). Collagen lattices were prepared by mixing cell suspensions with a neutralized solution of collagen type I matrix (8 parts Vitrogen100 collagen type I, 2.9 mg/ml, Collagen Corp, Santa Clara, CA, USA + 1 part 10 × α-MEM + 1 part HEPES buffer, pH 9.0). The cell-collagen concentrations were adjusted with sterile phosphate buffered solution (PBS) to attain a final collagen concentration of 2.0 mg/ml and a final cell concentration of 8.6 × 104 cells/ml of matrix. The cell-collagen mixture was then aliquoted into 24 well culture dishes (0.5 ml/well) that were pre-treated with a PBS solution containing 2% (w/v) bovine serum albumin (BSA). Following FPCL polymerization (1 hr, 37°C) culture medium (0.5 ml) consisting of α-MEM + 10% fetal bovine serum (FBS) was added atop each lattice. After 2 days of culture the attached FPCLs were mechanically released from the sides of the culture plates. Digital images of the contracting FPCL were captured at various time points over a 5-day assay period using a conventional flatbed scanner. Collagen lattice areas were then quantified using the Image J program . Each assay was done in quadruplicate.
Commercially available human recombinant TGF-β2 (expressed in NSO murine myeloma cells) was acid activated in a solution of 4N HCl + 0.1% (w/v) BSA according to the manufacturer's instructions (Product # T 2815, Sigma, St. Louis, MO). Acid activated human recombinant TGF-β2 was then aliquoted and frozen for extended storage at -70°C. The indicated concentrations of activated human recombinant TGF-β2 were added to complete culture media immediately following FPCL polymerization. Neutralizing anti-TGF-β2 antibodies (R&D Systems, Minneapolis, MN) were added to complete culture media either immediately following FPCL polymerization or added to the cell suspension prior to mixing with the neutralized Vitrogen collagen type I solution. Control FPCL cultures were treated with appropriate carrier solutions.
FPCL cultures were assayed using a commercially available CellTiter 96® Aqueous One Solution cell proliferation assay according to the manufacturer's instructions (Promega, Madison, WI, USA). This cell proliferation assay is a colorimetric method that uses a tetrazolium compound 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium salt (MTS) in combination with a stable electron coupling reagent PES (phenazine ethosulfate). This produces a chemically stable MTS tetrazolium compound that can be bio-reduced by cells to form a soluble colored formazan product [32, 33]. Briefly, cells from patient-matched primary cultures were cultured as stressed-relaxed FPCLs as described above. Each primary cell line was plated as quadruplicate FPCL cultures for each of the indicated time points with 0.5 ml of culture media ± TGF-β2 (1 ng/ml) atop each FPCL. At each of the designated contracting time points 100μl of CellTiter 96® Aqueous One solution reagent was added to the FPCL cultures and incubated for 3 hours (37°C, 5% CO2 atmosphere, humidified chamber). FPCL media was then collected and aliquoted into a 96-well culture plate for absorbance reading at 450 and 650 nm (background reference λ) using a 96-well BIO-RAD microplate reader. Media was also collected from FPCLs containing no cells (negative control) for background absorbance readings. The assay was conducted over 5 days during the course of FPCL contraction. A standard curve was also generated to calculate relative cell numbers per FPCL (range of 4 × 103–105 cells/FPCL).
Student two-tailed t test was used to compare data between two groups. Values were expressed as mean ± standard deviation of the mean (SDM). P values < 0.05 were considered statistically significant.
Members of the TGF-β family are potent fibrogenic factors that play an important role in the patho-physiology of numerous fibro-proliferative disorders, including DD . The study presented here focused on the effect of TGF-β2 on collagen contraction using primary FPCL cultures derived from patient-matched disease and control unaffected PF tissue. Here, we found that disease FPCL cultures contracted collagen faster and to a greater degree than patient-matched control FPCL cultures. Although neutralizing anti-TGF-β2 antibodies effectively blocked exogenous TGF-β2 stimulated FPCL contraction for both control and disease cultures, the same neutralizing antibodies had no effect on the basal collagen contraction activity of either disease or control FPCL cultures, suggesting that enhanced disease FPCL contraction is not due to elevated levels of endogenous active TGF-β2. These results, however, do not exclude the possibility that there may be differences in the levels of latent TGF-β2 produced by these cell cultures that may be subsequently activated in vivo. Recent work by Kuhn et. al. (2002) reported reduced DD FPCL contraction in response to tamoxifen, which was associated with a decreased TGF-β2 production . However, the TGF-β2 assayed in this study required an acid-activation step, suggesting that TGF-β2 produced by these cells is largely in its latent, non-activate form. Thus, it is possible that TGF-β2 produced by DD fibroblasts and/or other resident cell types in vivo may be important to disease cord contraction, provided appropriate regulators of latent TGF-β activation are also present and active. However, it does not explain the enhanced basal FPCL contraction rates of disease cell cultures, suggesting that other signalling factors may be regulating this disease cell function in vitro. It is interesting to note that both TGF-β and β-catenin signalling pathways show some degree of 'cross-talk' [29, 30, 36–38], suggesting that β-catenin plays an important role in TGF-β signalling. The degree and significance of signalling 'cross-talk' between β-catenin and TGF-β in the context of DD is unknown and needs further examination.
Although previous DD studies have used different 'control' primary fibroblast as 'disease-free' controls, namely fibroblasts derived from transverse carpal ligament material obtained from patients undergoing carpal tunnel release (CTR), they have the disadvantage of being of different anatomical origin than PF derived 'control' fibroblast cultures. This is an important consideration given that fibroblasts exhibit functional heterogeneity depending on their origin [39–41]. For example, human fibroblasts that express the cell surface antigen Thy-1 are capable of TGF-β1 stimulated myofibroblast differentiation, while Thy-1 negative fibroblasts appear to be only capable of lipofibroblast differentiation . Phenotypic differences have also been attributed to fibroblasts of different dermal origins . For example, Chipev and colleagues showed that TGF-β1 had a pro-apoptotic effect on non-palmoplantar (keloid) fibroblasts and an anti-apoptotic effect on palmoplantar fibroblasts. Similar to what we have observed for detached or contracting DD FPCL cultures, they showed that TGF-β1 treated (in the presence of serum) keloid FPCL cultures underwent the most extensive apoptosis response upon mechanical release compared to dermal fibroblasts from different body sites . Perhaps the similar myofibroblast phenotype attributed to both DD and keloid fibroblast cultures also dictates a similar apoptotic fate to relaxed FPCL cultures in response to TGF-βs. Although the loss of tension in these cultures triggered a mostly uniform loss in cell viability across all groups, unlike disease FPCL cultures TGF-β2 did not appear to have any significant pro-apoptotic effect on relaxed 'control' FPCL cultures. In light of these and other findings, it appears that the patient-matched control fibroblast cultures employed in these studies may truly represent a suitable 'control' phenotype, with the added advantage of having the same PF origins as the disease cell cultures. While this does not exclude the possibility that the control cultures may harbour some residual disease cells, this is not supported by the distinct phenotypic differences we have observed between these two types of patient-matched PF cultures in the current and previous studies. In these earlier studies, we reported elevated levels of β-catenin and fibronectin isoforms in disease FPCL cultures [22–24], as well as enhanced disease FPCL contraction rates which we have subsequently confirmed in these studies. This together with the distinctive pro-apoptotic affects of TGF-β2 on disease FPCL cultures described here, further support the notion that the patient/tissue-matched 'control' cultures have a non-disease phenotype that is suitable for these types of investigations.
Although the 'synthetic' myofibroblast features of the disease cells described in previous studies are known to be stimulated by TGF-β [20, 21, 25–30, 35], our results suggests that endogenous TGF-β2 does not play a role in regulating these phenotypic differences in vitro. Nevertheless, aberrant expression of various TGF-β signalling components have been previously shown to trigger this 'synthetic' myofibroblast phenotype in other fibro-proliferative disorders, specifically keloids and burn hypertrophic scarring [34, 44, 45], that can to some extent be inhibited by neutralizing anti-TGF-β2 antibodies [46, 47]. Hopefully future studies will unravel the extent of these phenotypic differences between these patient/tissue-matched control and disease FPCL cultures with respect to pro-fibrotic factors like TGF-β2, tension and other important intersecting signaling pathways.
Primary disease FPCL cultures contract collagen faster and to a greater extent than control PF-matched FPCL cultures. While neutralizing anti-TGF-β2 antibodies can block exogenous TGF-β2 stimulated collagen contraction for both control and disease FPCL cultures, it had no effect on the basal contraction rates of either control or disease FPCL cultures. We, therefore, conclude that the enhanced collagen contraction activity of disease FPCL cultures is not due to differences in the levels of endogenous active TGF-β2.
carpal tunnel release
transforming growth factor-beta
fibroblast populated collagen matrix
phosphate buffered saline
alpha-minimal essential medium
fetal bovine serum
reverse transcriptase polymerase chain reaction
standard deviation of the mean.
This study was supported by grants from the Canadian Institutes of Health Research, Plastic Surgery Education Fund, American Society for Surgery of the Hand, and the Lawson Health Research Institute's Internal Research Fund.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.