Literature DB >> 30051280

Fibroblast growth factor 21 induces lipolysis more efficiently than it suppresses lipogenesis in goat adipocytes.

Yongfeng Zhang1,2, Li Li1,2, Qin Wang1,2, Siyuan Zhan1,2, Linjie Wang1,2, Tao Zhong1,2, Jiazhong Guo1, Hongping Zhang3.   

Abstract

Fibroblast growth factor 21 (FGF21) potentially regulates glucose and lipid metabolism in energy homeostasis. We investigated dynamic changes in goat adipocytes treated with 75 nM FGF21 for 24, 36 and 48 h. Compared to controls, FGF21-treated adipocytes displayed smaller lipid droplets and altered levels of the mRNA transcripts encoding several lipolysis genes. The genes with elevated mRNA levels included: ATGL, HSL, CPT-1, and UCP1, and this was observed mainly at 24 and 36 h (P < 0.05). Some gene expression was attenuated including lipogenesis genes, such as SREBP1, PPARγ, C/EBPα, and ACC. This attenuation was observed mainly at 24 h (P < 0.05). Among the genes that were significantly induced or inhibited, ATGL, PGC1α, and C/EBPα were observed a significant effect at 48 h (P < 0.05). In addition, FGF21 treatment greatly increased number of mitochondria and the expression of genes implicated in mitochondrial biogenesis, such as PGC1α, NRF1, and TFAM. These results suggest that FGF21 treatment induced lipolysis more effectively than it suppressed lipogenesis in goat adipocytes, and that mitochondrial biogenesis plays an important role in these cells.

Entities:  

Keywords:  Adipocyte; FGF21; Lipogenesis; Lipolysis; Mitochondria

Year:  2018        PMID: 30051280      PMCID: PMC6214847          DOI: 10.1007/s10616-018-0237-1

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  43 in total

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8.  Fibroblast growth factor 21-deficient mice demonstrate impaired adaptation to ketosis.

Authors:  Michael K Badman; Anja Koester; Jeffrey S Flier; Alexei Kharitonenkov; Eleftheria Maratos-Flier
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