TNIIIA2, The Peptide of Tenascin-C, as a Candidate for Preventing Articular Cartilage Degeneration

Objective TNIIIA2 is a peptide of the extracellular matrix glycoprotein tenascin-C. We evaluated whether intra-articular injection of TNIIIA2 could prevent articular cartilage degeneration without inducing synovitis in an osteoarthritis mice model. Design Ten micrograms per milliliter of TNIIIA2 were injected into the knee joint of mice (group II) to evaluate the induction of synovitis. The control group received an injection of phosphate buffered saline (group I). Synovitis was evaluated using synovitis score 2 and 4 weeks after injection. The ligaments of knee joints of mice were transected to make the osteoarthritis model. After transection, 10 µg/mL of TNIIIA2 was injected into the knee joint (group IV). The control group received an injection of phosphate buffered saline after transection (group III). Histologic examinations were made using hematoxylin and eosin and safranin-O staining at 2, 4, 8, and 12 weeks postoperatively. An in vitro study was also performed to determine the mechanism by which TNIIIA2 prevents cartilage degeneration. Human chondrocytes were isolated, cultured, and treated with TNIIIA2. The expressions of various mRNAs, including inflammatory cytokines, and anabolic and catabolic factors for cartilage were compared using real-time polymerase chain reaction. Results There were no differences between groups in the study of intra-articular injection of mice (group I vs. group II). In the osteoarthritis model, we found development of osteoarthritis was suppressed in group IV at 4 and 8 weeks. TNIIIA2 upregulated the expressions of tumor necrosis factor-α, matrix metalloproteinase 3, and basic fibroblast growth factor. Conclusion We demonstrated that TNIIIA2 could prevent cartilage degeneration without synovitis.

[1]  A. Sudo,et al.  Tenascin-C promotes the repair of cartilage defects in mice. , 2020, Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association.

[2]  A. Sudo,et al.  Role of tenascin-C in articular cartilage , 2018, Modern rheumatology.

[3]  A. Sudo,et al.  Tenascin-C Prevents Articular Cartilage Degeneration in Murine Osteoarthritis Models , 2018, Cartilage.

[4]  A. Sudo,et al.  Effect of tenascin‐C on the repair of full‐thickness osteochondral defects of articular cartilage in rabbits , 2015, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[5]  Li Hao,et al.  Integrin-β1 regulates chondrocyte proliferation and apoptosis through the upregulation of GIT1 expression. , 2015, International journal of molecular medicine.

[6]  Caroline Tao,et al.  Adipocyte inflammation is essential for healthy adipose tissue expansion and remodeling. , 2014, Cell metabolism.

[7]  Johanne Martel-Pelletier,et al.  Role of proinflammatory cytokines in the pathophysiology of osteoarthritis , 2011, Nature Reviews Rheumatology.

[8]  A. Sudo,et al.  Distribution and role of tenascin-C in human osteoarthritic cartilage , 2010, Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association.

[9]  A. Sudo,et al.  Deficiency of tenascin-C delays articular cartilage repair in mice. , 2010, Osteoarthritis and cartilage.

[10]  M. Kashiwagi,et al.  Tenascin-C is an endogenous activator of Toll-like receptor 4 that is essential for maintaining inflammation in arthritic joint disease , 2009, Nature Medicine.

[11]  H. Handa,et al.  A Peptide Derived from Tenascin-C Induces β1 Integrin Activation through Syndecan-4* , 2007, Journal of Biological Chemistry.

[12]  G. Burmester,et al.  Synovitis score: discrimination between chronic low‐grade and high‐grade synovitis , 2006, Histopathology.

[13]  G. Orend Potential oncogenic action of tenascin-C in tumorigenesis. , 2005, The international journal of biochemistry & cell biology.

[14]  P. Jones,et al.  The tenascin family of ECM glycoproteins: Structure, function, and regulation during embryonic development and tissue remodeling , 2000, Developmental dynamics : an official publication of the American Association of Anatomists.

[15]  T. Sakakura,et al.  Involvement of tenascin-C in proliferation and migration of laryngeal carcinoma cells , 1999, Virchows Archiv.

[16]  D. Boettiger,et al.  Involvement of α5β1 Integrin in Matrix Interactions and Proliferation of Chondrocytes , 1997 .

[17]  Ken-ichi Matsumoto,et al.  Differential expression of tenascin-C and tenascin-X in human astrocytomas , 1997, Acta Neuropathologica.

[18]  D. Boettiger,et al.  Involvement of alpha5beta1 integrin in matrix interactions and proliferation of chondrocytes. , 1997, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[19]  L. Zardi,et al.  Tenascin distribution in articular cartilage from normal subjects and from patients with osteoarthritis and rheumatoid arthritis. , 1994, Arthritis and rheumatism.

[20]  H. Erickson,et al.  Cell- and heparin-binding domains of the hexabrachion arm identified by tenascin expression proteins. , 1993, The Journal of biological chemistry.

[21]  J. Spring,et al.  Two contrary functions of tenascin: Dissection of the active sites by recombinant tenascin fragments , 1989, Cell.

[22]  H. Dorfman,et al.  Biochemical and metabolic abnormalities in articular cartilage from osteo-arthritic human hips. II. Correlation of morphology with biochemical and metabolic data. , 1971, The Journal of bone and joint surgery. American volume.