دورية أكاديمية

Kindlin-2 loss in condylar chondrocytes causes spontaneous osteoarthritic lesions in the temporomandibular joint in mice

التفاصيل البيبلوغرافية
العنوان: Kindlin-2 loss in condylar chondrocytes causes spontaneous osteoarthritic lesions in the temporomandibular joint in mice
المؤلفون: Yumei Lai, Wei Zheng, Minghao Qu, Christopher C. Xiao, Sheng Chen, Qing Yao, Weiyuan Gong, Chu Tao, Qinnan Yan, Peijun Zhang, Xiaohao Wu, Guozhi Xiao
المصدر: International Journal of Oral Science, Vol 14, Iss 1, Pp 1-10 (2022)
بيانات النشر: Nature Publishing Group, 2022.
سنة النشر: 2022
المجموعة: LCC:Dentistry
مصطلحات موضوعية: Dentistry, RK1-715
الوصف: Abstract The progressive destruction of condylar cartilage is a hallmark of the temporomandibular joint (TMJ) osteoarthritis (OA); however, its mechanism is incompletely understood. Here, we show that Kindlin-2, a key focal adhesion protein, is strongly detected in cells of mandibular condylar cartilage in mice. We find that genetic ablation of Kindlin-2 in aggrecan-expressing condylar chondrocytes induces multiple spontaneous osteoarthritic lesions, including progressive cartilage loss and deformation, surface fissures, and ectopic cartilage and bone formation in TMJ. Kindlin-2 loss significantly downregulates the expression of aggrecan, Col2a1 and Proteoglycan 4 (Prg4), all anabolic extracellular matrix proteins, and promotes catabolic metabolism in TMJ cartilage by inducing expression of Runx2 and Mmp13 in condylar chondrocytes. Kindlin-2 loss decreases TMJ chondrocyte proliferation in condylar cartilages. Furthermore, Kindlin-2 loss promotes the release of cytochrome c as well as caspase 3 activation, and accelerates chondrocyte apoptosis in vitro and TMJ. Collectively, these findings reveal a crucial role of Kindlin-2 in condylar chondrocytes to maintain TMJ homeostasis.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1674-2818
2049-3169
العلاقة: https://doaj.org/toc/1674-2818Test; https://doaj.org/toc/2049-3169Test
DOI: 10.1038/s41368-022-00185-1
الوصول الحر: https://doaj.org/article/e511152728c54ceb868b6aafe19d408fTest
رقم الانضمام: edsdoj.511152728c54ceb868b6aafe19d408f
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:16742818
20493169
DOI:10.1038/s41368-022-00185-1