He Jingjing, Chen Daniel L, Samocha-Bonet Dorit, Gillinder Kevin R, Barclay Johanna L, Magor Graham W, Perkins Andrew C, Greenfield Jerry R, Yang Gongshe, Whitehead Jonathan P
a Laboratory of Animal Fat Deposition and Muscle Development , College of Animal Science and Technology, Northwest A&F University , Yangling , P.R. China.
b Mater Research Institute-University of Queensland, Translational Research Institute , Brisbane , Australia.
Growth Factors. 2016 Dec;34(5-6):210-216. doi: 10.1080/08977194.2017.1285764.
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.
成纤维细胞生长因子-1(FGF-1)通过调节骨形态发生蛋白和激活素膜结合抑制剂(BAMBI)/过氧化物酶体增殖物激活受体(PPARγ)依赖性网络,促进人脂肪前体细胞分化为成熟脂肪细胞。在此,我们结合转录组学和功能研究,以鉴定与人类脂肪组织基因表达的互补分析相一致的新型下游效应器,从而探索与胰岛素敏感性的关系。RNA测序和定量逆转录聚合酶链反应分析显示,在FGF-1处理或以不依赖BAMBI/PPARγ的方式诱导人脂肪前体细胞分化后,羧肽酶A4(CPA4)显著下调。小干扰RNA介导的CPA4敲低导致人脂肪前体细胞分化增强。此外,皮下脂肪组织中CPA4的表达与局部和全身(肝脏和肌肉)胰岛素敏感性指标呈负相关。这些结果确定CPA4是脂肪生成的负调节因子,其被FGF-1下调,并且是局部和全身胰岛素敏感性的假定有害调节因子。需要进一步研究来确定其中涉及的分子机制和潜在的治疗机会。