肌动蛋白细胞骨架是蛋白聚糖的调节器 4.

IF 2.7 4区 医学 Q1 ORTHOPEDICS
Sofia Gonzalez-Nolde, Cameron J Schweiger, Elizabeth E R Davis, Thomas J Manzoni, Samer M I Hussein, Tannin A Schmidt, Stephanie G Cone, Gregory D Jay, Justin Parreno
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引用次数: 0

摘要

目的:关节软骨表层区(SZ)负责分散剪切力,使软骨负荷达到最佳状态,并通过产生蛋白多糖 4(PRG4)促进关节润滑。PRG4 在关节稳态中发挥着关键作用,并具有软骨保护作用。在创伤后骨关节炎(PTOA)中,正常的 PRG4 生成会受到炎症和不规则机械负荷的影响。SZ软骨细胞(SZC)的表型,包括PRG4的表达,在体外受肌动蛋白细胞骨架的调控。人们对原生关节软骨细胞中肌动蛋白细胞骨架对 PRG4 的调控的了解仍然有限。丝状(F)肌动蛋白细胞骨架是机械刺激和细胞因子激活与深部软骨细胞中PRG4调控之间串联的潜在节点,因此深入了解肌动蛋白对PRG4的调控可能会发现新型PTOA疗法的分子靶点:对PRG4和肌动蛋白组织对SZC表型的调控进行了全面的文献检索:结果:PRG4在体外离体SZC中受到肌动蛋白细胞骨架的强烈调控。结论:基于肌动蛋白的PRG4调控在体外离体SZC中很强:结论:PRG4在原生SZC中基于肌动蛋白的调控尚未完全明了,需要进一步阐明。了解 SZCs 中肌动蛋白对 PRG4 的调控需要体内环境,以进一步挖掘利用肌动蛋白排列治疗关节炎的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Actin Cytoskeleton as a Regulator of Proteoglycan 4.

Objective: The superficial zone (SZ) of articular cartilage is responsible for distributing shear forces for optimal cartilage loading and contributes to joint lubrication through the production of proteoglycan 4 (PRG4). PRG4 plays a critical role in joint homeostasis and is chondroprotective. Normal PRG4 production is affected by inflammation and irregular mechanical loading in post-traumatic osteoarthritis (PTOA). THe SZ chondrocyte (SZC) phenotype, including PRG4 expression, is regulated by the actin cytoskeleton in vitro. There remains a limited understanding of the regulation of PRG4 by the actin cytoskeleton in native articular chondrocytes. The filamentous (F)-actin cytoskeleton is a potential node in crosstalk between mechanical stimulation and cytokine activation and the regulation of PRG4 in SZCs, therefore developing insights in the regulation of PRG4 by actin may identify molecular targets for novel PTOA therapies.

Materials and methods: A comprehensive literature search on PRG4 and the regulation of the SZC phenotype by actin organization was performed.

Results: PRG4 is strongly regulated by the actin cytoskeleton in isolated SZCs in vitro. Biochemical and mechanical stimuli have been characterized to regulate PRG4 and may converge upon actin cytoskeleton signaling.

Conclusion: Actin-based regulation of PRG4 in native SZCs is not fully understood and requires further elucidation. Understanding the regulation of PRG4 by actin in SZCs requires an in vivo context to further potential of leveraging actin arrangement to arthritic therapeutics.

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来源期刊
CARTILAGE
CARTILAGE ORTHOPEDICS-
CiteScore
6.90
自引率
7.10%
发文量
80
期刊介绍: CARTILAGE publishes articles related to the musculoskeletal system with particular attention to cartilage repair, development, function, degeneration, transplantation, and rehabilitation. The journal is a forum for the exchange of ideas for the many types of researchers and clinicians involved in cartilage biology and repair. A primary objective of CARTILAGE is to foster the cross-fertilization of the findings between clinical and basic sciences throughout the various disciplines involved in cartilage repair. The journal publishes full length original manuscripts on all types of cartilage including articular, nasal, auricular, tracheal/bronchial, and intervertebral disc fibrocartilage. Manuscripts on clinical and laboratory research are welcome. Review articles, editorials, and letters are also encouraged. The ICRS envisages CARTILAGE as a forum for the exchange of knowledge among clinicians, scientists, patients, and researchers. The International Cartilage Repair Society (ICRS) is dedicated to promotion, encouragement, and distribution of fundamental and applied research of cartilage in order to permit a better knowledge of function and dysfunction of articular cartilage and its repair.
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