The alchemy of tendon repair: a primer for the (S)mad scientist
http://www.100md.com
《临床调查学报》
1Department of Medicine, Division of Bone and Mineral Diseases and
2Department of Orthopedic Surgery, Washington University School of Medicine, St. Louis, Missouri, USA.
Abstract
During vertebrate development, mesenchymal progenitors capable of forming bone, cartilage, muscle, fat, or tendon arise from either neural crest or somitic mesoderm. Transcriptional programs that specify mesenchymal cell fates are initiated and modified by paracrine cues provided by TGF- superfamily members and mediated in part via the regulated assembly of Smad-containing multiprotein transcription factor complexes. In this issue of the JCI, Hoffmann and colleagues have identified that Smad8 activation drives tendon formation from C3H10T1/2 cells, a murine cell line that recapitulates many features of normal multipotent mesenchymal cells. Cells programmed to the tenocyte cell fate in vitro formed tenogenic grafts in vivo. These results add to the accumulating evidence that proliferating, multipotent mesenchymal progenitor cells can be programmed to yield multiple cell types — e.g., osteoblasts, myocytes, chondrocytes, and tenocytes — that may be useful in cell-based therapeutic approaches to musculoskeletal diseases.
See the related article beginning on page 940
Tendon and ligament injuries represent some of the most common musculoskeletal disorders that clinicians address daily, ranging from as mundane as a mild ankle sprain to the crippling effects of Achilles tendon rupture or flexor tendon injury in the hand (1). Severe tendon injuries are difficult to manage. Surgical repairs frequently do not fully restore function due to fibrous adhesions or failure arising from the mechanical demands placed on imperfect integrative healing at tendon-tendon or tendon-bone interfaces (1).
The tendon itself is a dense, regular connective tissue consisting primarily of type I collagen and the interspersed specialized mesenchymal cells known as tenocytes that are responsible for the maintenance of collagen structure, with avascular bundles of primary fibers invested by a thin layer of endotenon, a fine loose connective tissue sheath, to form fascicles (2) (Figure 1). Parallel arrays of fascicles are bundled together to form tendon by the epitenon, a layer contiguous with the endotenon through which the microvasculature, lymphatics, and innervation delicately traverses (2).
The ontogeny of the tenocyte lineage is only beginning to be understood. Elegant work recently forthcoming from the Tabin laboratory has demonstrated that during embryogenesis, a unique compartment of the somite called the syndetome provides tenocyte progenitors (3). Inductive interactions between the well-described myotome and sclerotome layers generate the syndetome, demarcated at the earliest stages of development by expression of the basic helix-loop-helix transcription factor gene Scleraxis. In addition to promoting tenocyte "birth," the myoprogenitors of the myotome appear to prevent chondrogenic differentiation of tenocyte progenitors. The paracrine signals that fine-tune multipotent mesenchymal progenitors to the unique tenocyte fate during normal development are virtually unknown, but appear to involve FGFs (3) and key members of the TGF- superfamily such as growth differentiation factor 5 (GDF5) and GDF7 (4).
A tenogenic Smad
Thus, given our limited understanding of how mesenchymal progenitors are efficiently recruited to the tenocyte lineage, the recent progress made by Hoffmann and colleagues in a report in this issue of the JCI is quite remarkable (5). Their insights into the mechanisms controlling tenocyte differentiation arose from fortuitous observations made while studying Smad signaling in C3H10T1/2 cells — a murine multipotent mesenchymal cell line that recapitulates many features of paraxial mesenchymal progenitors and can form osteoblasts, chondrocytes, adipocytes, or skeletal myocytes in culture (6, 7) (Figure 2A). Smads are a group of related intracellular proteins that transmit TGF- superfamily signals from ligand-activated cell surface receptors to the nucleus. Smads are related to, but structurally distinct from, other intracellular effector proteins and are composed of 3 domains: an N-terminal MH1 domain, a linker region, and a C-terminal MH2 domain (Figure 2B). Receptor-regulated Smads (R-Smads) associated with bone morphogenetic protein (BMP) signaling — Smad1, Smad5, and Smad8 — were expressed as constitutively active R-Smad linker plus MH2 domain (L+MH2) fragments lacking the N-terminal MH1 regulatory domain (8), and responses were assessed in the presence or absence of paracrine BMP2 signals (5). As previously shown (9), Smad1 and Smad5 directed alkaline phosphatase induction characteristic of osteoblast differentiation. By contrast, the Smad8 L+MH2 fragment markedly enhanced the adoption of tenocyte-like cell morphology, suggesting tenocytic differentiation. Consistent with this notion, the syndetome and tenocyte marker Scleraxis (3) was induced by the BMP2/Smad8 L+MH2 combination along with other characteristic tenocyte genes such as Six1, Six2, EphA4, and procollagen type I, 1 (Col1A1) (5). The expression of most osteogenic markers (e.g., parathyroid hormone/parathyroid hormone–related protein receptor and alkaline phosphatase) was downregulated by the BMP2/Smad8 L+MH2 tenocytic trigger, although osteocalcin expression was not. Intriguingly BMP2, but not TGF- or GDF5, could provide paracrine cues necessary for efficient tenocyte differentiation directed by Smad8 L+MH2. Importantly, C3H10T1/2 cells engineered to express both BMP2 and Smad8 L+MH2 provided gap replacement of tendon-like tissue in a rat tenotomy model. Cells expressing BMP2, Smad8 L+MH2, or the combination BMP2/Smad8 L+MH2 were introduced to a surgical partial-thickness Achilles tendon gap on an implantable collagen matrix sponge. Using histology and micro-MRI to monitor collagen fiber orientation and healing in vivo, the authors documented neotendon formation in implanted sponges carrying C3H10T1/2 cells programmed with BMP2/Smad8 L+MH2. No ectopic endochondral bone formation occurred, and laser capture microdissection and RT-PCR confirmed murine Col1A1 expression. By contrast, C3H10T1/2 cells programmed with only BMP2 generated ectopic bone and cartilage foci within the grafts, while Smad8 L+MH2 cells yielded only unorganized loose connective tissue. Immunohistochemistry to detect LacZ expression following adenovirus tagging and engraftment confirmed that the engineered BMP2/Smad8 L+MH2 cells did indeed contribute to the neotendon formed in vivo. Thus, the authors demonstrate the formation of tendon-like neotendon efficiently in vivo by BMP2 and Smad8 programming of mesenchymal progenitor cells (5).
The combinatorial conundrum
Many questions remain to be answered regarding the science of signal transduction and the needs of musculoskeletal medicine. It is unclear why paracrine BMP2 signaling is required to efficiently elaborate the full tenogenic potential of a constitutively active Smad8 L+MH2 fragment; it remains to be determined why removal of the MH1 domain — although capable of permitting Smad8 L+MH2 transactivation in transient transfection assays — is insufficient to promote robust tenogenesis in the absence of BMP2-generated signals. BMP2 receptor activation may trigger the phosphorylation-dependent nuclear transport and coregulator recruitment necessary for Smad8 tenogenic transcriptional complexes (8). While BMP2 clearly alters the phosphorylation of Smad8, it cannot activate full-length Smad8 — i.e., the intact MH1+L+MH2 molecule (Figure 2B) (5). Other regulatory receptor-ligand pairs presumably activate Smad8 in native context, perhaps mediated by a GDF family member other than GDF5 (4). GDF7 (also known as BMP12) has recently been shown to drive rhesus marrow mesenchymal cell differentiation to the tenocyte lineage in vitro (10). Of note, neither GDF5 nor TGF-1 were capable of enhancing Smad8 phosphorylation (5). Whether Smad8 participates in syndetome maturation and normal tendon development is as yet unknown. However, Smad8 signaling in mesenchymal cells is clearly not osteogenic and clearly drives gene expression programs different from those activated by Smad1 and Smad5. Indeed, Smad8 inhibits Smad1 and Smad5 signaling recruited by BMP4 during ventral mesoderm induction (11). While most artificially activated activin-like kinases can induce Smad8 phosphorylation, the "receptorology" of this R-Smad in vivo has yet to be determined.
A new opportunity in regenerative medicine
Of note, BMP2 enhances collagen production by canine tenocytes (12) and has been used to enhance tendon-bone integration in canine disease models (13). In this robustly validated preclinical model, surgical technique and postoperative physical therapy can be used to assess functional outcome and biomechanical strength (1) — the hallmarks of tendon repair that must be addressed in future studies. Immunologic and vascularization responses that influence the formation of fibrous adhesions may also be augmented by programmed neotendon cells and thus hamper restoration of function (14). Given that multipotent mesenchymal progenitors resembling C3H10T1/2 cells can be isolated from tissues such as adipose (15) and skeletal muscle (16), engineered autografts might be best explored in canine models of tendon injury repair to minimize the deleterious immune responses; such responses may limit healing, biomechanical strength, and restoration of function. Nevertheless, the novel results reported here by Hoffmann et al. (5) add to the accumulating evidence that proliferating, multipotent mesenchymal progenitor cells can be programmed to yield yet another cell type — the tenocyte — which may be potentially useful in cell-based therapeutic approaches to musculoskeletal injuries (1).
Footnotes
Nonstandard abbreviations used: BMP, bone morphogenetic protein; GDF, growth differentiation factor; L+MH2, R-Smad linker plus MH2 domain; R-Smad, receptor-regulated Smad.
Conflict of interest: The authors have declared that no conflict of interest exists.
References
Boyer, M.I., Goldfarb, C.A., and Gelberman, R.H. 2005. . Recent progress in flexor tendon healing. The modulation of tendon healing with rehabilitation variables. J. Hand Ther. 18::80-85; quiz 86.
Fenwick, S.A., Hazleman, B.L., and Riley, G.P. 2002. . The vasculature and its role in the damaged and healing tendon. Arthritis Res. 4::252-260.
Brent, A.E., Schweitzer, R., and Tabin, C.J. 2003. . A somitic compartment of tendon progenitors. Cell. 113::235-248.
Wolfman, N.M. et al. 1997. . Ectopic induction of tendon and ligament in rats by growth and differentiation factors 5, 6, and 7, members of the TGF- gene family. J. Clin. Invest. 100::321-330.
Hoffmann, A. et al. 2006. . Neotendon formation induced by manipulation of the Smad8 signalling pathway in mesenchymal stem cells. J. Clin. Invest. 116::940-952. doi:10.1172/JCI22689.
Cheng, S.L., Shao, J.S., Charlton-Kachigian, N., Loewy, A.P., and Towler, D.A. 2003. . MSX2 promotes osteogenesis and suppresses adipogenic differentiation of multipotent mesenchymal progenitors. J. Biol. Chem. 278::45969-45977.
Jasuja, R. et al. 2005. . Tetrahydrogestrinone is an androgenic steroid that stimulates androgen receptor-mediated, myogenic differentiation in C3H10T1/2 multipotent mesenchymal cells and promotes muscle accretion in orchidectomized male rats. Endocrinology. 146::4472-4478.
Massague, J., Seoane, J., and Wotton, D. 2005. . Smad transcription factors. Genes Dev. 19::2783-2810.
Yamamoto, N. et al. 1997. . Smad1 and smad5 act downstream of intracellular signalings of BMP-2 that inhibits myogenic differentiation and induces osteoblast differentiation in C2C12 myoblasts. Biochem. Biophys. Res. Commun. 238::574-580.
Wang, Q.W., Chen, Z.L., and Piao, Y.J. 2005. . Mesenchymal stem cells differentiate into tenocytes by bone morphogenetic protein (BMP) 12 gene transfer. J. Biosci. Bioeng. 100::418-422.
Nakayama, T. et al. 1998. . Xenopus Smad8 acts downstream of BMP-4 to modulate its activity during vertebrate embryonic patterning. Development. 125::857-867.
Thomopoulos, S., Harwood, F.L., Silva, M.J., Amiel, D., and Gelberman, R.H. 2005. . Effect of several growth factors on canine flexor tendon fibroblast proliferation and collagen synthesis in vitro. J. Hand Surg. (Am.). 30::441-447.
Martinek, V. et al. 2002. . Enhancement of tendon–bone integration of anterior cruciate ligament grafts with bone morphogenetic protein–2 gene transfer: a histological and biomechanical study. J. Bone Joint Surg. Am. 84::1123-1131.
Bidder, M., Towler, D.A., Gelberman, R.H., and Boyer, M.I. 2000. . Expression of mRNA for vascular endothelial growth factor at the repair site of healing canine flexor tendon. J. Orthop. Res. 18::247-252.
Zuk, P.A. et al. 2002. . Human adipose tissue is a source of multipotent stem cells. Mol. Biol. Cell. 13::4279-4295.
Lee, J.Y. et al. 2000. . Clonal isolation of muscle-derived cells capable of enhancing muscle regeneration and bone healing. J. Cell Biol. 150::1085-1100.
Related Article
Neotendon formation induced by manipulation of the Smad8 signalling pathway in mesenchymal stem cells
Andrea Hoffmann, Gadi Pelled, Gadi Turgeman, Peter Eberle, Yoram Zilberman, Hadassah Shinar, Keren Keinan-Adamsky, Andreas Winkel, Sandra Shahab, Gil Navon, Gerhard Gross, and Dan Gazit
J. Clin. Invest. 2006 116: 940-952.(Dwight A. Towler and Rich)
2Department of Orthopedic Surgery, Washington University School of Medicine, St. Louis, Missouri, USA.
Abstract
During vertebrate development, mesenchymal progenitors capable of forming bone, cartilage, muscle, fat, or tendon arise from either neural crest or somitic mesoderm. Transcriptional programs that specify mesenchymal cell fates are initiated and modified by paracrine cues provided by TGF- superfamily members and mediated in part via the regulated assembly of Smad-containing multiprotein transcription factor complexes. In this issue of the JCI, Hoffmann and colleagues have identified that Smad8 activation drives tendon formation from C3H10T1/2 cells, a murine cell line that recapitulates many features of normal multipotent mesenchymal cells. Cells programmed to the tenocyte cell fate in vitro formed tenogenic grafts in vivo. These results add to the accumulating evidence that proliferating, multipotent mesenchymal progenitor cells can be programmed to yield multiple cell types — e.g., osteoblasts, myocytes, chondrocytes, and tenocytes — that may be useful in cell-based therapeutic approaches to musculoskeletal diseases.
See the related article beginning on page 940
Tendon and ligament injuries represent some of the most common musculoskeletal disorders that clinicians address daily, ranging from as mundane as a mild ankle sprain to the crippling effects of Achilles tendon rupture or flexor tendon injury in the hand (1). Severe tendon injuries are difficult to manage. Surgical repairs frequently do not fully restore function due to fibrous adhesions or failure arising from the mechanical demands placed on imperfect integrative healing at tendon-tendon or tendon-bone interfaces (1).
The tendon itself is a dense, regular connective tissue consisting primarily of type I collagen and the interspersed specialized mesenchymal cells known as tenocytes that are responsible for the maintenance of collagen structure, with avascular bundles of primary fibers invested by a thin layer of endotenon, a fine loose connective tissue sheath, to form fascicles (2) (Figure 1). Parallel arrays of fascicles are bundled together to form tendon by the epitenon, a layer contiguous with the endotenon through which the microvasculature, lymphatics, and innervation delicately traverses (2).
The ontogeny of the tenocyte lineage is only beginning to be understood. Elegant work recently forthcoming from the Tabin laboratory has demonstrated that during embryogenesis, a unique compartment of the somite called the syndetome provides tenocyte progenitors (3). Inductive interactions between the well-described myotome and sclerotome layers generate the syndetome, demarcated at the earliest stages of development by expression of the basic helix-loop-helix transcription factor gene Scleraxis. In addition to promoting tenocyte "birth," the myoprogenitors of the myotome appear to prevent chondrogenic differentiation of tenocyte progenitors. The paracrine signals that fine-tune multipotent mesenchymal progenitors to the unique tenocyte fate during normal development are virtually unknown, but appear to involve FGFs (3) and key members of the TGF- superfamily such as growth differentiation factor 5 (GDF5) and GDF7 (4).
A tenogenic Smad
Thus, given our limited understanding of how mesenchymal progenitors are efficiently recruited to the tenocyte lineage, the recent progress made by Hoffmann and colleagues in a report in this issue of the JCI is quite remarkable (5). Their insights into the mechanisms controlling tenocyte differentiation arose from fortuitous observations made while studying Smad signaling in C3H10T1/2 cells — a murine multipotent mesenchymal cell line that recapitulates many features of paraxial mesenchymal progenitors and can form osteoblasts, chondrocytes, adipocytes, or skeletal myocytes in culture (6, 7) (Figure 2A). Smads are a group of related intracellular proteins that transmit TGF- superfamily signals from ligand-activated cell surface receptors to the nucleus. Smads are related to, but structurally distinct from, other intracellular effector proteins and are composed of 3 domains: an N-terminal MH1 domain, a linker region, and a C-terminal MH2 domain (Figure 2B). Receptor-regulated Smads (R-Smads) associated with bone morphogenetic protein (BMP) signaling — Smad1, Smad5, and Smad8 — were expressed as constitutively active R-Smad linker plus MH2 domain (L+MH2) fragments lacking the N-terminal MH1 regulatory domain (8), and responses were assessed in the presence or absence of paracrine BMP2 signals (5). As previously shown (9), Smad1 and Smad5 directed alkaline phosphatase induction characteristic of osteoblast differentiation. By contrast, the Smad8 L+MH2 fragment markedly enhanced the adoption of tenocyte-like cell morphology, suggesting tenocytic differentiation. Consistent with this notion, the syndetome and tenocyte marker Scleraxis (3) was induced by the BMP2/Smad8 L+MH2 combination along with other characteristic tenocyte genes such as Six1, Six2, EphA4, and procollagen type I, 1 (Col1A1) (5). The expression of most osteogenic markers (e.g., parathyroid hormone/parathyroid hormone–related protein receptor and alkaline phosphatase) was downregulated by the BMP2/Smad8 L+MH2 tenocytic trigger, although osteocalcin expression was not. Intriguingly BMP2, but not TGF- or GDF5, could provide paracrine cues necessary for efficient tenocyte differentiation directed by Smad8 L+MH2. Importantly, C3H10T1/2 cells engineered to express both BMP2 and Smad8 L+MH2 provided gap replacement of tendon-like tissue in a rat tenotomy model. Cells expressing BMP2, Smad8 L+MH2, or the combination BMP2/Smad8 L+MH2 were introduced to a surgical partial-thickness Achilles tendon gap on an implantable collagen matrix sponge. Using histology and micro-MRI to monitor collagen fiber orientation and healing in vivo, the authors documented neotendon formation in implanted sponges carrying C3H10T1/2 cells programmed with BMP2/Smad8 L+MH2. No ectopic endochondral bone formation occurred, and laser capture microdissection and RT-PCR confirmed murine Col1A1 expression. By contrast, C3H10T1/2 cells programmed with only BMP2 generated ectopic bone and cartilage foci within the grafts, while Smad8 L+MH2 cells yielded only unorganized loose connective tissue. Immunohistochemistry to detect LacZ expression following adenovirus tagging and engraftment confirmed that the engineered BMP2/Smad8 L+MH2 cells did indeed contribute to the neotendon formed in vivo. Thus, the authors demonstrate the formation of tendon-like neotendon efficiently in vivo by BMP2 and Smad8 programming of mesenchymal progenitor cells (5).
The combinatorial conundrum
Many questions remain to be answered regarding the science of signal transduction and the needs of musculoskeletal medicine. It is unclear why paracrine BMP2 signaling is required to efficiently elaborate the full tenogenic potential of a constitutively active Smad8 L+MH2 fragment; it remains to be determined why removal of the MH1 domain — although capable of permitting Smad8 L+MH2 transactivation in transient transfection assays — is insufficient to promote robust tenogenesis in the absence of BMP2-generated signals. BMP2 receptor activation may trigger the phosphorylation-dependent nuclear transport and coregulator recruitment necessary for Smad8 tenogenic transcriptional complexes (8). While BMP2 clearly alters the phosphorylation of Smad8, it cannot activate full-length Smad8 — i.e., the intact MH1+L+MH2 molecule (Figure 2B) (5). Other regulatory receptor-ligand pairs presumably activate Smad8 in native context, perhaps mediated by a GDF family member other than GDF5 (4). GDF7 (also known as BMP12) has recently been shown to drive rhesus marrow mesenchymal cell differentiation to the tenocyte lineage in vitro (10). Of note, neither GDF5 nor TGF-1 were capable of enhancing Smad8 phosphorylation (5). Whether Smad8 participates in syndetome maturation and normal tendon development is as yet unknown. However, Smad8 signaling in mesenchymal cells is clearly not osteogenic and clearly drives gene expression programs different from those activated by Smad1 and Smad5. Indeed, Smad8 inhibits Smad1 and Smad5 signaling recruited by BMP4 during ventral mesoderm induction (11). While most artificially activated activin-like kinases can induce Smad8 phosphorylation, the "receptorology" of this R-Smad in vivo has yet to be determined.
A new opportunity in regenerative medicine
Of note, BMP2 enhances collagen production by canine tenocytes (12) and has been used to enhance tendon-bone integration in canine disease models (13). In this robustly validated preclinical model, surgical technique and postoperative physical therapy can be used to assess functional outcome and biomechanical strength (1) — the hallmarks of tendon repair that must be addressed in future studies. Immunologic and vascularization responses that influence the formation of fibrous adhesions may also be augmented by programmed neotendon cells and thus hamper restoration of function (14). Given that multipotent mesenchymal progenitors resembling C3H10T1/2 cells can be isolated from tissues such as adipose (15) and skeletal muscle (16), engineered autografts might be best explored in canine models of tendon injury repair to minimize the deleterious immune responses; such responses may limit healing, biomechanical strength, and restoration of function. Nevertheless, the novel results reported here by Hoffmann et al. (5) add to the accumulating evidence that proliferating, multipotent mesenchymal progenitor cells can be programmed to yield yet another cell type — the tenocyte — which may be potentially useful in cell-based therapeutic approaches to musculoskeletal injuries (1).
Footnotes
Nonstandard abbreviations used: BMP, bone morphogenetic protein; GDF, growth differentiation factor; L+MH2, R-Smad linker plus MH2 domain; R-Smad, receptor-regulated Smad.
Conflict of interest: The authors have declared that no conflict of interest exists.
References
Boyer, M.I., Goldfarb, C.A., and Gelberman, R.H. 2005. . Recent progress in flexor tendon healing. The modulation of tendon healing with rehabilitation variables. J. Hand Ther. 18::80-85; quiz 86.
Fenwick, S.A., Hazleman, B.L., and Riley, G.P. 2002. . The vasculature and its role in the damaged and healing tendon. Arthritis Res. 4::252-260.
Brent, A.E., Schweitzer, R., and Tabin, C.J. 2003. . A somitic compartment of tendon progenitors. Cell. 113::235-248.
Wolfman, N.M. et al. 1997. . Ectopic induction of tendon and ligament in rats by growth and differentiation factors 5, 6, and 7, members of the TGF- gene family. J. Clin. Invest. 100::321-330.
Hoffmann, A. et al. 2006. . Neotendon formation induced by manipulation of the Smad8 signalling pathway in mesenchymal stem cells. J. Clin. Invest. 116::940-952. doi:10.1172/JCI22689.
Cheng, S.L., Shao, J.S., Charlton-Kachigian, N., Loewy, A.P., and Towler, D.A. 2003. . MSX2 promotes osteogenesis and suppresses adipogenic differentiation of multipotent mesenchymal progenitors. J. Biol. Chem. 278::45969-45977.
Jasuja, R. et al. 2005. . Tetrahydrogestrinone is an androgenic steroid that stimulates androgen receptor-mediated, myogenic differentiation in C3H10T1/2 multipotent mesenchymal cells and promotes muscle accretion in orchidectomized male rats. Endocrinology. 146::4472-4478.
Massague, J., Seoane, J., and Wotton, D. 2005. . Smad transcription factors. Genes Dev. 19::2783-2810.
Yamamoto, N. et al. 1997. . Smad1 and smad5 act downstream of intracellular signalings of BMP-2 that inhibits myogenic differentiation and induces osteoblast differentiation in C2C12 myoblasts. Biochem. Biophys. Res. Commun. 238::574-580.
Wang, Q.W., Chen, Z.L., and Piao, Y.J. 2005. . Mesenchymal stem cells differentiate into tenocytes by bone morphogenetic protein (BMP) 12 gene transfer. J. Biosci. Bioeng. 100::418-422.
Nakayama, T. et al. 1998. . Xenopus Smad8 acts downstream of BMP-4 to modulate its activity during vertebrate embryonic patterning. Development. 125::857-867.
Thomopoulos, S., Harwood, F.L., Silva, M.J., Amiel, D., and Gelberman, R.H. 2005. . Effect of several growth factors on canine flexor tendon fibroblast proliferation and collagen synthesis in vitro. J. Hand Surg. (Am.). 30::441-447.
Martinek, V. et al. 2002. . Enhancement of tendon–bone integration of anterior cruciate ligament grafts with bone morphogenetic protein–2 gene transfer: a histological and biomechanical study. J. Bone Joint Surg. Am. 84::1123-1131.
Bidder, M., Towler, D.A., Gelberman, R.H., and Boyer, M.I. 2000. . Expression of mRNA for vascular endothelial growth factor at the repair site of healing canine flexor tendon. J. Orthop. Res. 18::247-252.
Zuk, P.A. et al. 2002. . Human adipose tissue is a source of multipotent stem cells. Mol. Biol. Cell. 13::4279-4295.
Lee, J.Y. et al. 2000. . Clonal isolation of muscle-derived cells capable of enhancing muscle regeneration and bone healing. J. Cell Biol. 150::1085-1100.
Related Article
Neotendon formation induced by manipulation of the Smad8 signalling pathway in mesenchymal stem cells
Andrea Hoffmann, Gadi Pelled, Gadi Turgeman, Peter Eberle, Yoram Zilberman, Hadassah Shinar, Keren Keinan-Adamsky, Andreas Winkel, Sandra Shahab, Gil Navon, Gerhard Gross, and Dan Gazit
J. Clin. Invest. 2006 116: 940-952.(Dwight A. Towler and Rich)