دورية أكاديمية

Distinctive roles of tumor necrosis factor receptor type 1 and type 2 in a mouse disc degeneration model

التفاصيل البيبلوغرافية
العنوان: Distinctive roles of tumor necrosis factor receptor type 1 and type 2 in a mouse disc degeneration model
المؤلفون: Shanzheng Wang, Guodong Sun, Pan Fan, Lei Huang, Yaofei Chen, Changhong Chen
المصدر: Journal of Orthopaedic Translation, Vol 31, Iss , Pp 62-72 (2021)
بيانات النشر: Elsevier, 2021.
سنة النشر: 2021
المجموعة: LCC:Diseases of the musculoskeletal system
مصطلحات موضوعية: Intervertebral disc degeneration, Tumor Necrosis Factor-α, TNF receptor type 1, TNF receptor type 2, Progranulin, Atsttrin, Diseases of the musculoskeletal system, RC925-935
الوصف: Background: Elevated tumor necrosis factor alpha (TNF-α) expression is correlated with the progression of intervertebral disc degeneration (IVDD). Progranulin binding to tumor necrosis factor receptor (TNFR) and its derivative Atsttrin are effective for treating inflammatory arthritis. We hypothesize that Atsttrin has a protective effect in IVDD through different roles of TNFR receptor type 1 (TNFR1) and TNFR receptor type 2 (TNFR2) in degenerated discs. Methods: IVDD models were established in TNFR1−/−, TNFR2−/− mice and their control littermates. Nucleus Pulpous (NP) samples from human patients and IVDD murine models were evaluated by X-ray, micro-MRI, μCT, histological staining and immunofluorescence staining. NP cells isolated from wild-type (WT), TNFR1−/− and TNFR2−/− mice were treated with TNF-α or Atsttrin and then assayed by Western blotting, qRT–PCR, and ELISA. Results: TNFR1 and TNFR2 expression was significantly elevated in the disc tissues of both human patients and IVDD murine models. TNFR1 knockout contributed to reduced disc degeneration. In contrast, TNFR2 knockout was associated with enhanced IVDD severity, including degraded cellular composition, increased cell apoptosis and elevated vertebral destruction. Atsttrin protected against IVDD in WT and TNFR1−/− mouse models but had no effect in TNFR2−/− IVDD models. Additionally, in vitro NP cell-based assays demonstrated that TNF-α-stimulated catabolism and Atsttrin-activated anabolism depended on TNFR1 and TNFR2, respectively. Conclusion: TNFR1 is associated with the degenerative progression of IVDD, while TNFR2 contributes to the protective effect on the discs. Atsttrin protects against IVDD at least partially by inhibiting the TNFα/TNFR1 inflammatory/catabolic pathway and activating the TNFR2 protective/anabolic pathway. The translational potential of this article: This study demonstrates that TNFR1 and TNFR2 have disparate roles in disc degeneration and hlights the potential use of Atsttrin as a therapeutic agent against IVDD in mice.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2214-031X
العلاقة: http://www.sciencedirect.com/science/article/pii/S2214031X21000954Test; https://doaj.org/toc/2214-031XTest
DOI: 10.1016/j.jot.2021.11.003
الوصول الحر: https://doaj.org/article/9857b067f1c54e2a897f7f6453973e34Test
رقم الانضمام: edsdoj.9857b067f1c54e2a897f7f6453973e34
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:2214031X
DOI:10.1016/j.jot.2021.11.003