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RhoB 通过信号素 3A/神经丛蛋白 A4 促进早孕子宫内膜基质细胞蜕膜化。

RhoB Promotes Endometrial Stromal Cells Decidualization Via Semaphorin3A/PlexinA4 Signaling in Early Pregnancy.

机构信息

NHC Key Lab of Reproduction Regulation (Shanghai Institute of Planned Parenthood Research), Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases, Hospital of Obstetrics and Gynecology, Fudan University Shanghai Medical College, Shanghai, China.

Laboratory for Reproductive Immunology, Hospital of Obstetrics and Gynecology, Fudan University Shanghai Medical College, Shanghai, China.

出版信息

Endocrinology. 2022 Oct 11;163(11). doi: 10.1210/endocr/bqac134.

Abstract

Endometrial decidualization refers to a series of morphological changes and functional remodeling of the uterine endometrium to accept the embryo under the effect of estrogen and progesterone secreted by ovaries after ovulation. During decidualization, endometrial stromal cells (ESCs) proliferate and differentiate into decidual stromal cells, undergoing cytoskeletal rearrangement-mediated morphological changes and expressing decidualization markers, such as insulin-like growth factor-binding protein-1 and prolactin. Ras homology (Rho) proteins, a family of small G proteins, are well known as regulators of cellular morphology and involved in multiple other cellular processes. In this study, we found ras homolog family member B (RHOB) was the most significantly upregulated gene in the Rho protein family after the in vitro decidualization of human primary ESCs. RhoB expression was induced mainly by 3',5'-cyclic adenosine 5'-monophosphate (cAMP) / protein kinase A (PKA) / cyclic adenosine monophosphate-response element binding protein signaling and partly by progesterone signaling. Knockdown of RhoB in ESCs greatly inhibited actin cytoskeletal rearrangement, cell morphological transformation, and upregulation of insulin-like growth factor-binding protein-1, suggesting an indispensable role of RhoB in decidualization. Mechanistically, the downstream target of RhoB was semaphorin3A (Sema3A), which mediated its signaling via interacting with the receptor, plexinA4. More importantly, decreased expression of RhoB, Sema3A, and plexinA4 were detected in deciduas from patients with unexplained spontaneous miscarriage. Collectively, our results indicate that RhoB/Sema3A/plexinA4 signaling plays a positive role in endometrial decidualization and relates to unexplained spontaneous miscarriage, which is worthy of further exploration so as to provide new insights into therapeutic strategies for pregnancy diseases associated with poor decidualization.

摘要

子宫内膜蜕膜化是指在卵巢排卵后分泌的雌激素和孕激素的作用下,子宫子宫内膜发生一系列形态变化和功能重塑,以接受胚胎。在蜕膜化过程中,子宫内膜基质细胞(ESCs)增殖并分化为蜕膜基质细胞,经历细胞骨架重排介导的形态变化,并表达蜕膜化标志物,如胰岛素样生长因子结合蛋白-1和催乳素。Ras 同源(Rho)蛋白家族是一类小 G 蛋白,作为细胞形态的调节剂而闻名,并参与许多其他细胞过程。在这项研究中,我们发现 ras 同源家族成员 B(RHOB)是 Rho 蛋白家族中在人原代 ESCs 体外蜕膜化后上调最显著的基因。RhoB 的表达主要由 3',5'-环磷酸腺苷(cAMP)/蛋白激酶 A(PKA)/环磷酸腺苷反应元件结合蛋白信号转导诱导,部分由孕激素信号转导诱导。在 ESCs 中敲低 RhoB 会极大地抑制肌动蛋白细胞骨架重排、细胞形态转化和胰岛素样生长因子结合蛋白-1 的上调,表明 RhoB 在蜕膜化中不可或缺。从机制上讲,RhoB 的下游靶标是神经纤毛蛋白 3A(Sema3A),它通过与受体plexinA4 相互作用来介导其信号转导。更重要的是,在不明原因自然流产患者的蜕膜中检测到 RhoB、Sema3A 和 plexinA4 的表达减少。总之,我们的研究结果表明,RhoB/Sema3A/plexinA4 信号在子宫内膜蜕膜化中发挥积极作用,并与不明原因自然流产有关,这值得进一步探索,以便为与蜕膜不良相关的妊娠疾病的治疗策略提供新的见解。

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