Fibroblast growth factor-1 (FGF-1) promotes adipogenesis by downregulation of carboxypeptidase A4 (CPA4) – a negative regulator of adipogenesis implicated in the modulation of local and systemic insulin sensitivity

脂肪生成 内分泌学 脂肪组织 内科学 FGF21型 成纤维细胞生长因子 下调和上调 基因敲除 调节器 生物 细胞生物学 生长因子 胰岛素 化学 受体 基因 医学 生物化学
作者
Jingjing He,Daniel L. Chen,Dorit Samocha‐Bonet,Kevin R. Gillinder,Johanna L. Barclay,Graham Magor,Andrew C. Perkins,Jerry R. Greenfield,Gongshe Yang,Jonathan P. Whitehead
出处
期刊:Growth Factors Journal [Taylor & Francis]
卷期号:34 (5-6): 210-216 被引量:14
标识
DOI:10.1080/08977194.2017.1285764
摘要

Fibroblast growth factor-1 (FGF-1) promotes differentiation of human preadipocytes into mature adipocytes via modulation of a BMP and Activin Membrane-Bound Inhibitor (BAMBI)/Peroxisome proliferator-activated receptor (PPARγ)-dependent network. Here, we combined transcriptomic and functional investigations to identify novel downstream effectors aligned with complementary analyses of gene expression in human adipose tissue to explore relationships with insulin sensitivity. RNA-Seq and qRT-PCR analysis revealed significant down-regulation of carboxypeptidase A4 (CPA4) following FGF-1 treatment or induction of differentiation of human preadipocytes in a BAMBI/PPARγ-independent manner. siRNA-mediated knockdown of CPA4 resulted in enhanced differentiation of human preadipocytes. Furthermore, expression of CPA4 in subcutaneous adipose tissue correlated negatively with indices of local and systemic (liver and muscle) insulin sensitivity. These results identify CPA4 as a negative regulator of adipogenesis that is down-regulated by FGF-1 and a putative deleterious modulator of local and systemic insulin sensitivity. Further investigations are required to define the molecular mechanism(s) involved and potential therapeutic opportunities.

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