首页> 外文OA文献 >Luteinizing Hormone Receptor-Stimulated Progesterone Production by Preovulatory Granulosa Cells Requires Protein Kinase A-Dependent Activation/Dephosphorylation of the Actin Dynamizing Protein Cofilin
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Luteinizing Hormone Receptor-Stimulated Progesterone Production by Preovulatory Granulosa Cells Requires Protein Kinase A-Dependent Activation/Dephosphorylation of the Actin Dynamizing Protein Cofilin

机译:排卵前颗粒细胞促黄体激素受体刺激的孕酮生产需要蛋白激酶A依赖的肌动蛋白活化蛋白Cofilin的激活/去磷酸化

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摘要

Activation of the LH receptor (LHR) on preovulatory granulosa cells stimulates the cAMP/protein kinase A (PKA) pathway to regulate expression of genes required for ovulation and luteinization. LHR signaling also initiates rearrangement of the actin cytoskeleton. Because disruption of the actin cytoskeleton has been causally linked to steroidogenesis in various cell models, we sought to identify the cellular mechanisms that may modulate reorganization of the actin cytoskeleton and to determine whether cytoskeletal reorganization is required for steroidogenesis. Herein we report that LHR signaling in preovulatory granulosa cells promotes rapid dephosphorylation of the actin-depolymerizing factor cofilin at Ser3 that is dependent on PKA. The LHR-stimulated dephosphorylation of cofilin(Ser3) switches on cofilin activity to bind actin filaments and enhance their dynamics. Basal phosphorylation of cofilin(Ser3) is mediated by active/GTP-bound Rho and downstream protein kinases; LHR signaling promotes a decrease in active/GTP-bound Rho by a PKA-dependent mechanism. LHR-dependent Rho inactivation and subsequent activation of cofilin does not involve ERK, epidermal growth factor receptor, or phosphatidylinositol 3-kinase pathways downstream of PKA. To understand the biological significance of cofilin activation, preovulatory granulosa cells were transduced with a mutant cofilin adenoviral vector in which Ser3 was mutated to Glu (S-E cofilin). Inactive S-E cofilin abolished LHR-mediated reorganization of the actin cytoskeleton and caused a 70% decrease in LHR-stimulated progesterone that is obligatory for ovulation. Taken together, these results show that LHR signaling via PKA activates a cofilin-regulated rearrangement of the actin cytoskeleton and that active cofilin is required to initiate progesterone secretion by preovulatory granulosa cells.
机译:排卵前颗粒细胞上LH受体(LHR)的激活刺激cAMP /蛋白激酶A(PKA)通路,调节排卵和黄体化所需基因的表达。 LHR信号转导也引发肌动蛋白细胞骨架的重排。由于肌动蛋白细胞骨架的破坏已与各种细胞模型中的类固醇生成有因果关系,因此我们试图确定可调节肌动蛋白细胞骨架重组的细胞机制,并确定类固醇生成是否需要细胞骨架重组。本文中我们报道排卵前颗粒细胞中的LHR信号促进了依赖于PKA的Ser3上肌动蛋白解聚因子cofilin的快速去磷酸化。 LHR刺激的cofilin(Ser3)的去磷酸化可切换cofilin活性以结合肌动蛋白丝并增强其动力学。活化/ GTP结合的Rho和下游蛋白激酶介导cofilin(Ser3)的基础磷酸化; LHR信号通过依赖PKA的机制促进活性/ GTP结合的Rho降低。依赖LHR的Rho失活以及随后的cofilin激活不涉及PKA下游的ERK,表皮生长因子受体或磷脂酰肌醇3激酶途径。为了了解cofilin激活的生物学意义,用突变的cofilin腺病毒载体转导了排卵前的颗粒细胞,其中Ser3突变为Glu(S-E cofilin)。无效的S-E纤溶蛋白消除了LHR介导的肌动蛋白细胞骨架的重组,并导致LHR刺激的黄体酮减少70%,这是排卵所必须的。综上所述,这些结果表明,经由PKA的LHR信号激活了肌动蛋白细胞骨架的cofilin调节的重排,并且需要主动cofilin来启动排卵前颗粒细胞分泌孕酮。

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