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Recent progress on the role of cellular communication network factors (CCN) 3, 4 and 6 in regulating adiposity, liver fibrosis and pancreatic islets.
Xega, Viktoria; Alami, Tara; Liu, Jun-Li.
Afiliação
  • Xega V; MeDiC Program, The Research Institute of McGill University Health Centre, 1001 Decarie Blvd, Montreal, QC, H4A 3J1, Canada.
  • Alami T; Division of Endocrinology and Metabolism, Department of Medicine, McGill University, Montreal, QC, H4A 3J1, Canada.
  • Liu JL; MeDiC Program, The Research Institute of McGill University Health Centre, 1001 Decarie Blvd, Montreal, QC, H4A 3J1, Canada.
J Cell Commun Signal ; 17(2): 297-306, 2023 Jun.
Article em En | MEDLINE | ID: mdl-37245185
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article