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胶原蛋白和非胶原蛋白在骨质疏松症病理生理学中的分子对话。

Collagen and non-collagenous proteins molecular crosstalk in the pathophysiology of osteoporosis.

机构信息

Department of Applied Science and Technology, Politecnico di Torino, Corso Duca degli Abruzzi 24, 10129, Torino, Italy; Department of Clinical and Molecular Sciences (DISCLIMO), Università Politecnica delle Marche, Via Tronto 10/a, 60126, Ancona, Italy.

Department of Applied Science and Technology, Politecnico di Torino, Corso Duca degli Abruzzi 24, 10129, Torino, Italy.

出版信息

Cytokine Growth Factor Rev. 2019 Oct;49:59-69. doi: 10.1016/j.cytogfr.2019.09.001. Epub 2019 Sep 13.

Abstract

Collagenous and non-collagenous proteins (NCPs) in the extracellular matrix, as well as the coupling mechanisms between osteoclasts and osteoblasts, work together to ensure normal bone metabolism. Each protein plays one or more critical roles in bone metabolism, sometimes even contradictory, thus affecting the final mechanical, physical and chemical properties of bone tissue. Anomalies in the amount and structure of one or more of these proteins can cause abnormalities in bone formation and resorption, which consequently leads to malformations and defects, such as osteoporosis (OP). The connections between key proteins involved in matrix formation and resorption are far from being elucidated. In this review, we resume knowledge on the crosstalk between collagen type I and selected NCPs (Transforming Growth Factor-β, Insulin-like Growth Factor-1, Decorin, Osteonectin, Osteopontin, Bone Sialoprotein and Osteocalcin) of bone matrix, focusing on their possible involvement and role in OP. The different elements of this network can be pharmacologically targeted or used for the design/development of innovative regenerative strategies to modulate a feedback loop in bone remodelling.

摘要

细胞外基质中的胶原和非胶原蛋白(NCPs),以及破骨细胞和成骨细胞之间的偶联机制,共同作用以确保正常的骨代谢。每种蛋白在骨代谢中发挥一个或多个关键作用,有时甚至相互矛盾,从而影响骨组织的最终机械、物理和化学性质。这些蛋白中的一种或多种的数量和结构异常可导致骨形成和吸收异常,从而导致畸形和缺陷,如骨质疏松症(OP)。参与基质形成和吸收的关键蛋白之间的联系远未阐明。在这篇综述中,我们总结了骨基质中 I 型胶原与选定的 NCPs(转化生长因子-β、胰岛素样生长因子-1、核心蛋白聚糖、骨连接蛋白、骨桥蛋白、骨唾液蛋白和骨钙素)之间的串扰知识,重点关注它们在 OP 中的可能参与和作用。该网络的不同元素可以进行药理学靶向或用于设计/开发创新的再生策略,以调节骨重塑中的反馈环。

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