Medical Research Laboratory, Department of Clinical Medicine, Health, Aarhus University, Aarhus, Denmark.
Department of Endocrinology, Aarhus University Hospital, Aarhus, Denmark.
Physiol Rep. 2020 Feb;8(3):e14373. doi: 10.14814/phy2.14373.
Since GH stimulates lipolysis in vivo after a 2-hr lag phase, we studied whether this involves GH signaling and gene expression in adipose tissue (AT).
Human subjects (n = 9) each underwent intravenous exposure to GH versus saline with measurement of serum FFA, and GH signaling, gene array, and protein in AT biopsies after 30-120 min. Human data were corroborated in adipose-specific GH receptor knockout (FaGHRKO) mice versus wild-type mice. Expression of candidate genes identified in the array were investigated in 3T3-L1 adipocytes.
GH increased serum FFA and AT phosphorylation of STAT5b in human subjects. This was replicated in wild-type mice, but not in FaGHRKO mice. The array identified 53 GH-regulated genes, and Ingenuity Pathway analysis showed downregulation of PDE3b, an insulin-dependent antilipolytic signal, upregulation of PTEN that inhibits insulin-dependent antilipolysis, and downregulation of G0S2 and RASD1, both encoding antilipolytic proteins. This was confirmed in 3T3-L1 adipocytes, except for PDE3B, including reciprocal effects of GH and insulin on mRNA expression of PTEN, RASD1, and G0S2.
(a) GH directly stimulates AT lipolysis in a GHR-dependent manner, (b) this involves suppression of antilipolytic signals at the level of gene expression, (c) the underlying GH signaling pathways remain to be defined.
由于 GH 在经历 2 小时的滞后阶段后会在体内刺激脂肪分解,我们研究了这是否涉及脂肪组织 (AT) 中的 GH 信号转导和基因表达。
9 名受试者每人接受静脉内 GH 暴露与盐水暴露,在 30-120 分钟后测量血清 FFA 以及 AT 活检中的 GH 信号转导、基因阵列和蛋白质。人类数据在脂肪特异性 GH 受体敲除 (FaGHRKO) 小鼠与野生型小鼠中得到证实。在 3T3-L1 脂肪细胞中研究了阵列中鉴定出的候选基因的表达。
GH 增加了人体血清 FFA 和 AT 中 STAT5b 的磷酸化。这在野生型小鼠中得到了复制,但在 FaGHRKO 小鼠中没有。该阵列鉴定出 53 个 GH 调节基因,Ingenuity 通路分析显示 PDE3b 的下调,PDE3b 是一种依赖胰岛素的抗脂肪分解信号,PTEN 的上调抑制依赖胰岛素的抗脂肪分解,以及 G0S2 和 RASD1 的下调,两者均编码抗脂肪分解蛋白。这在 3T3-L1 脂肪细胞中得到了证实,除了 PDE3B 之外,还包括 GH 和胰岛素对 PTEN、RASD1 和 G0S2 mRNA 表达的相互作用。
(a) GH 以 GHR 依赖的方式直接刺激 AT 脂肪分解,(b) 这涉及基因表达水平上抗脂肪分解信号的抑制,(c) 潜在的 GH 信号通路仍有待确定。