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α2-巨球蛋白通过诱导增殖细胞核抗原促进软骨细胞增殖和软骨基质合成。

α2-Macroglobulin Promotes Chondrocyte Proliferation and Cartilage Matrix Synthesis via Inducing PCNA.

作者信息

Guo Hailing, Wang Shaowei, Zhang Yang, Sun Jian, Guo Li, Pang Jian, Zhan Hongsheng

机构信息

Shi's Center of Orthopedics and Traumatology, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.

Institute of Traumatology & Orthopedics, Shanghai Academy of Traditional Chinese Medicine, Shanghai, China.

出版信息

Cartilage. 2025 Jun;16(2):202-211. doi: 10.1177/19476035231207776. Epub 2023 Oct 23.

Abstract

Objectivesα2-Macroglobulin (A2M) can prevent cartilage degeneration by blocking many types of cartilage-degrading enzymes, but the mechanism remains to be clarified. This study aimed to test that A2M protects against cartilage degeneration by promoting chondrocyte proliferation and cartilage matrix synthesis via inducing proliferating cell nuclear antigen (PCNA).DesignThe cartilage degeneration of the anterior cruciate ligament transection (ACLT) model was evaluated by Safranin O-fast green staining, and articular cartilage degeneration was graded using the Osteoarthritis Research Society International (OARSI)-modified Mankin criteria. The chondrocyte proliferation was detected by 5-Bromodeoxyuridinc (BrdU), MTT, and Cell Counting Kit-8 (CCK8) methods. The chondrocyte apoptosis was detected by lactate dehydrogenase (LDH) assay and Annexin PI staining with the flow cytometer. The glycosaminoglycan (sGAG) and aggrecan in culture supernatant were measured by enzyme-linked immunosorbent assay (ELISA). Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) was used to analyze the type II collagen and aggrecan mRNA expression. The PCNA protein expression was analyzed by western blot and immunofluorescent staining.ResultsA2M can attenuate cartilage degeneration in ACLT rats. The OARSI scores for cartilage degeneration in the A2M group were lower than those in the phosphate-buffered saline (PBS) group. A2M can promote chondrocyte proliferation and inhibit chondrocyte apoptosis, promote the cartilage matrix synthesis in chondrocytes (type II collagen and aggrecan), and culture supernatant (sGAG and aggrecan). At the same time, it also up-regulated the PCNA protein expression in chondrocytes.ConclusionsA2M can promote chondrocyte proliferation and cartilage matrix synthesis via inducing PCNA expression.

摘要

目的α2-巨球蛋白(A2M)可通过阻断多种软骨降解酶来预防软骨退变,但其机制仍有待阐明。本研究旨在验证A2M通过诱导增殖细胞核抗原(PCNA)促进软骨细胞增殖和软骨基质合成,从而预防软骨退变。

设计采用番红O-固绿染色评估前交叉韧带横断(ACLT)模型的软骨退变情况,并使用国际骨关节炎研究学会(OARSI)改良的曼金标准对关节软骨退变进行分级。通过5-溴脱氧尿嘧啶核苷(BrdU)、MTT和细胞计数试剂盒-8(CCK8)方法检测软骨细胞增殖情况。通过乳酸脱氢酶(LDH)测定和流式细胞仪Annexin PI染色检测软骨细胞凋亡情况。采用酶联免疫吸附测定(ELISA)法测定培养上清液中的糖胺聚糖(sGAG)和聚集蛋白聚糖。采用逆转录定量聚合酶链反应(RT-qPCR)分析Ⅱ型胶原和聚集蛋白聚糖mRNA表达。通过蛋白质印迹法和免疫荧光染色分析PCNA蛋白表达。

结果A2M可减轻ACLT大鼠的软骨退变。A2M组软骨退变的OARSI评分低于磷酸盐缓冲盐水(PBS)组。A2M可促进软骨细胞增殖,抑制软骨细胞凋亡,促进软骨细胞(Ⅱ型胶原和聚集蛋白聚糖)和培养上清液(sGAG和聚集蛋白聚糖)中的软骨基质合成。同时,它还上调了软骨细胞中PCNA蛋白的表达。

结论A2M可通过诱导PCNA表达促进软骨细胞增殖和软骨基质合成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd89/12066844/109c4ca37fc5/10.1177_19476035231207776-fig1.jpg

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