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Nonmuscle myosin IIA (myosin heavy polypeptide 9): a novel class of signal transducer mediating the activation of G alpha h/phospholipase C-delta 1 pathway.

机译:非肌肉肌球蛋白IIA(肌球蛋白重多肽9):一类新型的信号转导子,介导G alpha h /磷脂酶C-delta 1途径的激活。

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摘要

The dimeric Gh protein is comprised of alpha (tissue transglutaminase) and beta (Calreticulin) subunits and known to be associated with FSH-, oxytocin-, or epinephrine-receptors/functions in their respective target cells. After establishing the FSH-induced activation of G alpha h/phospholipase C (PLC)-delta 1 pathway in rat Sertoli cells (SCs), we have attempted to identify a possible G alpha h-coupled novel FSH receptor (FSH-R). Remarkably, a protein with approximately 240-kDa molecular mass was coimmunoprecipitated with G alpha h in the fractionated membrane proteins of rat SCs. The protein was identified as myosin heavy polypeptide 9 (MyH9) by mass spectrometric analysis and immunoblotting. In addition, immunoprecipitation analysis reveals that MyH9 is constitutively associated with classical Gs-coupled FSH-R and inactive GDP-bound G alpha h at resting state of rat SCs, but did not interact with FSH directly as judged by Far-Western analysis. Upon the stimulation of higher levels of extracellular FSH (>1000 IU/liter), classical FSH-R induces the phosphorylation of MyH9, the dissociation of active GTP-bound G alpha h from FSH-R:MyH9 complexes, and the elicitation of G alpha h/PLC-delta 1 pathway-dependent Ca(2+)-influx in rat SCs. Furthermore, the specific inhibition of MyH9 ATPase activity with Blebbistatin dose-dependently suppressed FSH-induced G alpha h/PLC-delta 1 signaling and Ca(2+)-influx, but not intracellular cAMP accumulation in rat SCs, implying that MyH9 mediates FSH-induced activation of G alpha h/PLC-delta 1/IP(3)/Ca(2+)-influx pathway in rat SCs. This is the first to demonstrate that the filament protein MyH9 constitutively forms a ternary complex with FSH-R and inactive GDP-bound G alpha h. At higher FSH levels, this ternary complex executes an alternative signaling of classical Gs-coupled FSH-R through activating a Gs/cAMP-independent, G alpha h/PLC-delta 1 pathway in rat SCs.
机译:二聚体Gh蛋白由α(组织转谷氨酰胺酶)和β(钙网蛋白)亚基组成,已知与各自靶细胞中的FSH,催产素或肾上腺素受体/功能有关。在大鼠支持细胞(SC)中建立FSH诱导的Gαh /磷脂酶C(PLC)-δ1途径的激活后,我们试图鉴定可能的Gαh偶联的新型FSH受体(FSH-R)。值得注意的是,在大鼠SC的分离膜蛋白中,分子量约为240 kDa的蛋白与G alpha h共免疫沉淀。通过质谱分析和免疫印迹将该蛋白鉴定为肌球蛋白重多肽9(MyH9)。此外,免疫沉淀分析表明,在大鼠SC的静止状态下,MyH9与经典的Gs偶联的FSH-R和无活性的GDP结合的G alpha h组成性相关,但未根据Far-Western分析判断与FSH直接相互作用。在刺激更高水平的细胞外FSH(> 1000 IU /升)后,经典的FSH-R诱导MyH9磷酸化,活性GTP结合的G alpha h从FSH-R:MyH9复合物中解离,并诱导G在大鼠SC中的alpha h / PLC-delta 1途径依赖性Ca(2+)流入。此外,Blebbistatin对MyH9 ATPase活性的特异性抑制作用可剂量依赖性地抑制FSH诱导的G alpha h / PLC-delta 1信号传导和Ca(2+)流入,但不抑制大鼠SC中的细胞内cAMP积累,这意味着MyH9介导FSH。诱导大鼠SCs中的G alpha h /PLC-δ1 / IP(3)/ Ca(2 +)-流入途径的激活。这是第一个证明细丝蛋白MyH9与FSH-R和无活性的GDP结合的G alpha h构成三元复合物。在较高的FSH水平下,该三元复合物通过激活大鼠SC中的Gs / cAMP独立的G alpha h / PLC-delta 1途径,执行经典的Gs-偶联的FSH-R的替代信号传导。

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