Recent progress on the role of cellular communication network factors (CCN) 3, 4 and 6 in regulating adiposity, liver fibrosis and pancreatic islets

IF 3.6 3区 生物学 Q3 CELL BIOLOGY
Viktoria Xega, Tara Alami, Jun-Li Liu
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引用次数: 1

Abstract

CCN/WISP (cellular communication network factors, or Wnt-inducted secreted proteins) family of proteins consists of six extracellular matrix (ECM)-associated proteins that regulate development, cell adhesion and proliferation, ECM remodeling, inflammation, and tumorigenesis. In the last two decades, metabolic regulation by these matricellular proteins has been studied extensively, several excellent reviews have covered the roles of CCN1, -2 and − 5. In this brief review, we will focus on those lesser-known members and more recent discoveries, together with other recent articles presenting a more complete picture of the current state of knowledge. We have found that CCN2, -4, and − 5 promote pancreatic islet function, while CCN3 plays a unique and negative role. CCN3 and − 4 are pro-adiposity leading to insulin resistance, but CCN5 and − 6 are anti-adiposity. While CCN2 and − 4 promote tissue fibrosis and inflammation, all other four members are clearly anti-fibrotic. As for cellular signaling, they are known to interact with integrins, other cell membrane proteins and ECM thereby regulate Akt/protein kinase B, myocardin-related transcription factor (MRTF), and focal adhesion kinase. Yet, a cohesive mechanism of action to comprehensively explain those major functions is still lacking.

细胞通讯网络因子(CCN) 3,4和6在肥胖、肝纤维化和胰岛调节中的作用研究进展
CCN/WISP(细胞通信网络因子,或wnt诱导分泌蛋白)蛋白家族由六种细胞外基质(ECM)相关蛋白组成,这些蛋白调节发育、细胞粘附和增殖、ECM重塑、炎症和肿瘤发生。在过去的二十年中,这些基质细胞蛋白的代谢调节已经得到了广泛的研究,一些优秀的综述已经涵盖了CCN1, -2和- 5的作用。在这篇简短的综述中,我们将重点关注那些不太为人所知的成员和最近的发现,以及其他最近的文章,这些文章展示了当前知识状态的更完整的图景。我们发现CCN2、-4和- 5促进胰岛功能,而CCN3发挥独特的负作用。CCN3和- 4是促肥胖导致胰岛素抵抗,而CCN5和- 6是抗肥胖。虽然CCN2和- 4促进组织纤维化和炎症,但其他四种成员都明显具有抗纤维化作用。在细胞信号方面,已知它们与整合素、其他细胞膜蛋白和ECM相互作用,从而调节Akt/蛋白激酶B、心肌素相关转录因子(MRTF)和局灶黏附激酶。然而,目前还缺乏一个连贯的作用机制来全面解释这些主要功能。
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来源期刊
CiteScore
6.40
自引率
4.90%
发文量
40
期刊介绍: The Journal of Cell Communication and Signaling provides a forum for fundamental and translational research. In particular, it publishes papers discussing intercellular and intracellular signaling pathways that are particularly important to understand how cells interact with each other and with the surrounding environment, and how cellular behavior contributes to pathological states. JCCS encourages the submission of research manuscripts, timely reviews and short commentaries discussing recent publications, key developments and controversies. Research manuscripts can be published under two different sections : In the Pathology and Translational Research Section (Section Editor Andrew Leask) , manuscripts report original research dealing with celllular aspects of normal and pathological signaling and communication, with a particular interest in translational research. In the Molecular Signaling Section (Section Editor Satoshi Kubota) manuscripts report original signaling research performed at molecular levels with a particular interest in the functions of intracellular and membrane components involved in cell signaling.
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