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

被引:3
作者
Xega, Viktoria [1 ,2 ]
Alami, Tara [1 ,2 ]
Liu, Jun-Li [1 ,2 ]
机构
[1] McGill Univ, Med Program, Res Inst, Hlth Ctr, 1001 Decarie Blvd, Montreal, PQ H4A 3J1, Canada
[2] McGill Univ, Dept Med, Div Endocrinol & Metab, Montreal, PQ H4A 3J1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Matricellular proteins; Integrins; Inflammation; Insulin resistance; Knockout; Mitogen-activated protein kinase (MAPK); SIGNALING PATHWAY PROTEIN-1; GROWTH-FACTOR CTGF; GENE-EXPRESSION; BETA-CELLS; PROLIFERATION; CCN1/CYR61; SENESCENCE; INDUCTION; BIOMARKER; MODEL;
D O I
10.1007/s12079-023-00765-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:297 / 306
页数:10
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