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在小鼠模型中,促黄体生成素可维持原始阶段暴露于烷化剂化疗的生长卵泡中卵母细胞-颗粒细胞的通讯。

Luteinizing Hormone Preserves Oocyte-Granulosa Cell Communication in Growing Follicles Exposed to Chemotherapy with Alkylating Agents at the Primordial Stage in a Mouse Model.

作者信息

Del Castillo Luis Miguel, Ramírez-Martín Noelia, Soriano María José, Martínez Jessica, Pellicer Nuria, Pellicer Antonio, Herraiz Sonia

机构信息

Department of Pediatrics, Obstetrics and Gynecology, School of Medicine, University of Valencia, 46010, Valencia, Spain.

IVIRMA Global Research Alliance, IVI Foundation, Instituto de Investigación Sanitaria La Fe (IIS La Fe), 46026, Valencia, Spain.

出版信息

Reprod Sci. 2025 Aug 6. doi: 10.1007/s43032-025-01936-1.

Abstract

Reciprocal communication between the oocyte and adjacent granulosa cells (GC) throughout folliculogenesis can be disrupted by chemotherapy. Recent work suggests that luteinizing hormone (LH) may protect the quality of metaphase-II oocytes derived from primordial follicles exposed to chemotherapy in mice. Here, we showed that LH improved the follicular yield of CD1 mice ovaries exposed to alkylating chemotherapy by primarily protecting the smallest follicles, i.e., the primordial and primary populations. LH treatment reverted the chemotherapy-induced impairment of oocyte-GC communication at the gene and protein levels in secondary and later-stage follicles exposed to alkylating chemotherapy at the primordial phase by preserving the germ and somatic cell compartments. These changes are follicle-specific, as supported by the absence of differences in ovarian stroma. LH also restored the immunofluorescence signal for cell junction proteins Cx37, E-Cad and Cx43, and for oocyte-secreted factors GDF9 and BMP15. The alteration of signal intensity associated with these cell junction proteins and oocyte-secreted factors by chemotherapy was detected beyond the secondary stage, suggesting that attenuation of oocyte-GC crosstalk might happen during the primary-secondary transition. Our results suggest that LH-treated primordial follicles retain the ability to properly establish oocyte-GC interactions and crosstalk during follicular growth representing a novel mechanism triggered by LH that would explain the reported protective effects of LH on oocyte quality and female fertility. However, this is an animal model study that should be validated in larger studies with human samples.

摘要

在整个卵泡发生过程中,卵母细胞与相邻颗粒细胞(GC)之间的相互通讯可能会被化疗破坏。最近的研究表明,促黄体生成素(LH)可能会保护小鼠中来自暴露于化疗的原始卵泡的中期II期卵母细胞的质量。在这里,我们表明,LH主要通过保护最小的卵泡,即原始卵泡和初级卵泡群体,提高了暴露于烷化化疗的CD1小鼠卵巢的卵泡产量。LH处理通过保留生殖细胞和体细胞区室,在基因和蛋白质水平上逆转了原始阶段暴露于烷化化疗的次级及后期卵泡中化疗诱导的卵母细胞-GC通讯损伤。这些变化是卵泡特异性的,卵巢基质中没有差异支持了这一点。LH还恢复了细胞连接蛋白Cx37、E-钙黏蛋白和Cx43以及卵母细胞分泌因子GDF9和BMP15的免疫荧光信号。化疗对这些细胞连接蛋白和卵母细胞分泌因子信号强度的改变在次级阶段之后被检测到,这表明卵母细胞-GC串扰的减弱可能发生在初级-次级转变期间。我们的结果表明,LH处理的原始卵泡在卵泡生长过程中保留了正确建立卵母细胞-GC相互作用和串扰的能力,这代表了一种由LH触发的新机制,该机制可以解释LH对卵母细胞质量和女性生育能力的保护作用。然而,这是一项动物模型研究,应该在更大规模的人体样本研究中进行验证。

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