| First Author | Chen R | Year | 2015 |
| Journal | Am J Pathol | Volume | 185 |
| Issue | 11 | Pages | 2875-85 |
| PubMed ID | 26355014 | Mgi Jnum | J:227013 |
| Mgi Id | MGI:5699513 | Doi | 10.1016/j.ajpath.2015.07.003 |
| Citation | Chen R, et al. (2015) Attenuation of the Progression of Articular Cartilage Degeneration by Inhibition of TGF-beta1 Signaling in a Mouse Model of Osteoarthritis. Am J Pathol 185(11):2875-85 |
| abstractText | Transforming growth factor beta 1 (TGF-beta1) is implicated in osteoarthritis. We therefore studied the role of TGF-beta1 signaling in the development of osteoarthritis in a developmental stage-dependent manner. Three different mouse models were investigated. First, the Tgf-beta receptor II (Tgfbr2) was specifically removed from the mature cartilage of joints. Tgfbr2-deficient mice were grown to 12 months of age and were then euthanized for collection of knee and temporomandibular joints. Second, Tgfbr2-deficient mice were subjected to destabilization of the medial meniscus (DMM) surgery. Knee joints were then collected from the mice at 8 and 16 weeks after the surgery. Third, wild-type mice were subjected to DMM at the age of 8 weeks. Immediately after the surgery, these mice were treated with the Tgfbr2 inhibitor losartan for 8 weeks and then euthanized for collection of knee joints. All joints were characterized for evidences of articular cartilage degeneration. Initiation or acceleration of articular cartilage degeneration was not observed by the genetic inactivation of Tgfbr2 in the joints at the age of 12 months. In fact, the removal of Tgfbr2 and treatment with losartan both delayed the progression of articular cartilage degeneration induced by DMM compared with control littermates. Therefore, we conclude that inhibition of Tgf-beta1 signaling protects adult knee joints in mice against the development of osteoarthritis. |
