Xu Jie, Messina Joseph L
Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama 35294-0019, USA.
Vitam Horm. 2009;80:125-53. doi: 10.1016/S0083-6729(08)00606-7.
Growth Hormone (GH) is a major growth-promoting and metabolic regulatory hormone. Interaction of GH with its cell surface GH receptor (GHR) causes activation of the GHR-associated cytoplasmic tyrosine kinase, JAK2, and activation of several signaling pathways, including the STATs, ERK1/2, and PI3K pathways. Insulin is also a key hormone regulating metabolism and growth. Insulin binding to the insulin receptor (IR) results in phosphorylation/activation of the IR, and activates the PI3K/Akt and ERK1/2 pathways. Due to their important roles in growth and metabolism, GH and insulin can functionally interact with each other, regulating cellular metabolism. In addition, recent data suggests that GH and insulin can directly interact by signaling crosstalk. Insulin regulation of GH signaling depends on the duration of exposure to insulin. Transient insulin exposure enhances GH-induced activation of MEK/ERK pathway through post-GHR mechanisms, whereas prolonged insulin exposure inhibits GH-induced signaling at both receptor and postreceptor levels. Chronic excessive GH interferes with insulin's activation of the IR/IRS/PI3K pathway and several proteins are involved in the mechanisms underlying GH-induced insulin resistance.
生长激素(GH)是一种主要的促进生长和调节代谢的激素。GH与其细胞表面生长激素受体(GHR)相互作用,导致与GHR相关的细胞质酪氨酸激酶JAK2激活,并激活包括信号转导和转录激活因子(STATs)、细胞外信号调节激酶1/2(ERK1/2)和磷脂酰肌醇-3激酶(PI3K)途径在内的多种信号通路。胰岛素也是调节代谢和生长的关键激素。胰岛素与胰岛素受体(IR)结合会导致IR磷酸化/激活,并激活PI3K/Akt和ERK1/2途径。由于GH和胰岛素在生长和代谢中发挥重要作用,它们在功能上可以相互作用,调节细胞代谢。此外,最近的数据表明,GH和胰岛素可通过信号串扰直接相互作用。胰岛素对GH信号的调节取决于胰岛素暴露的持续时间。短暂的胰岛素暴露通过GHR后的机制增强GH诱导的MEK/ERK途径激活,而长时间的胰岛素暴露在受体和受体后水平均抑制GH诱导的信号传导。慢性过量的GH会干扰胰岛素对IR/胰岛素受体底物(IRS)/PI3K途径的激活,并且几种蛋白质参与了GH诱导的胰岛素抵抗的潜在机制。