肥胖和2型糖尿病:骨骼肌细胞外基质重塑的启示。

IF 5 2区 生物学 Q2 CELL BIOLOGY
Linda Wu, Dawn K Coletta
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引用次数: 0

摘要

肥胖和2型糖尿病(T2DM)是流行的代谢性疾病。这些疾病的经济负担处于历史最高水平,因此,迫切需要在确定治疗这些复杂疾病的目标方面取得进展。细胞外基质(ECM)由胶原蛋白、纤维连接蛋白、层粘连蛋白、弹性蛋白和蛋白多糖组成,围绕在骨骼肌周围,通过提供结构支持和促进细胞间通讯,在维持组织稳态中起着关键作用。ECM信号的破坏导致其微/宏观环境的改变,从而改变组织的稳态。骨骼肌ECM重塑已被证明与胰岛素抵抗有关,胰岛素抵抗是肥胖和2型糖尿病的潜在特征。本文综述了骨骼肌ECM的关键组成部分及其在代谢性疾病中的积累和重塑。此外,我们还讨论了减轻骨骼肌ECM重塑影响的潜在治疗方法。我们的结论是,针对骨骼肌的ECM重塑代表了代谢紊乱管理中一个有希望但尚未开发的治疗途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Obesity and type 2 diabetes mellitus: insights from skeletal muscle extracellular matrix remodeling.

Obesity and type 2 diabetes mellitus (T2DM) are metabolic diseases at epidemic proportions. The economic burden for these diseases is at an all-time high, and as such, there is an urgent need for advancements in identifying targets for treating these complex disorders. The extracellular matrix (ECM), comprising collagen, fibronectin, laminin, elastin, and proteoglycan, surrounds skeletal muscles and plays a critical role in maintaining tissue homeostasis by providing structural support and facilitating cell-to-cell communication. Disruption of the ECM signaling results in changes to its micro/macroenvironment, thereby modifying tissue homeostasis. Skeletal muscle ECM remodeling has been shown to be associated with insulin resistance, an underlying feature of obesity and T2DM. This narrative review explores the critical components of skeletal muscle ECM and its accumulation and remodeling in metabolic diseases. In addition, we discuss potential treatments to mitigate the effects of ECM remodeling in skeletal muscle. We conclude that targeting ECM remodeling in skeletal muscle represents a promising yet underexplored therapeutic avenue in the management of metabolic disorders.

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来源期刊
CiteScore
9.10
自引率
1.80%
发文量
252
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. Contributions that use cellular and molecular approaches to shed light on mechanisms of physiological control at higher levels of organization also appear regularly. Manuscripts dealing with the structure and function of cell membranes, contractile systems, cellular organelles, and membrane channels, transporters, and pumps are encouraged. Studies dealing with integrated regulation of cellular function, including mechanisms of signal transduction, development, gene expression, cell-to-cell interactions, and the cell physiology of pathophysiological states, are also eagerly sought. Interdisciplinary studies that apply the approaches of biochemistry, biophysics, molecular biology, morphology, and immunology to the determination of new principles in cell physiology are especially welcome.
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