Aoyama Masato, Shiraishi Akira, Matsubara Shin, Horie Kaoru, Osugi Tomohiro, Kawada Tsuyoshi, Yasuda Keiko, Satake Honoo
Department of Chemistry, Biology, and Environmental Science, Faculty of Science, Nara Women's University, Nara, Japan.
Bioorganic Research Institute, Suntory Foundation for Life Sciences, Kyoto, Japan.
Front Endocrinol (Lausanne). 2019 Aug 14;10:553. doi: 10.3389/fendo.2019.00553. eCollection 2019.
Theca/interstitial cells are responsible for the growth and maturation of ovarian follicles. However, little is known about the theca/interstitial cell-specific genes and their functions. In this study, we explored transcriptomes of theca/interstitial cells by RNA-seq, and the novel biological roles of a theca cell marker, asporin (Aspn)/periodontal ligament-associated protein 1 (PLAP-1). RNA-seq detected 432 and 62 genes expressed specifically in theca/interstitial cells and granulosa cells isolated from 3-weeks old mouse ovaries. Gene ontology analysis demonstrated that these genes were largely categorized into four major groups: extracellular matrix organization-related terms, chemotaxis-related terms, the angiogenesis-related terms, and morphogenesis-related terms. hybridization demonstrated that the newly detected representative gene, , was detected specifically in the outer layer of theca cells in contrast with the expression of the basal lamina-specific gene, Nidgen-1. Intriguingly, an Aspn/PLAP-1 antibody completely arrested the growth of secondary follicles that is the gonadotropin-independent follicle developmental stage. Furthermore, transforming growth factor-β (TGF-β)-triggered signaling was induced by the Aspn/PLAP-1 antibody treatment, which is consistent with the inhibitory effect of Aspn/PLAP-1 on TGF-β. Altogether, these results suggest that theca cells are classified into subpopulations on the basis of new marker genes and their biological functions, and provide evidence that Aspn/PLAP-1 is expressed exclusively in the outer layer of theca cells and plays a pivotal role in the growth of secondary follicles via downregulation of the canonical TGF-β signaling cascade.
卵泡膜/间质细胞负责卵巢卵泡的生长和成熟。然而,关于卵泡膜/间质细胞特异性基因及其功能却知之甚少。在本研究中,我们通过RNA测序探索了卵泡膜/间质细胞的转录组,以及卵泡膜细胞标志物骨桥蛋白(Aspn)/牙周膜相关蛋白1(PLAP-1)的新生物学作用。RNA测序检测到从3周龄小鼠卵巢分离的卵泡膜/间质细胞和颗粒细胞中分别有432个和62个特异性表达的基因。基因本体分析表明,这些基因主要分为四大类:细胞外基质组织相关术语、趋化性相关术语、血管生成相关术语和形态发生相关术语。原位杂交表明,与基底膜特异性基因Nidgen-1的表达相反,新检测到的代表性基因Aspn/PLAP-1在卵泡膜细胞外层特异性表达。有趣的是,一种Aspn/PLAP-1抗体完全抑制了次级卵泡的生长,次级卵泡处于不依赖促性腺激素的卵泡发育阶段。此外,Aspn/PLAP-1抗体处理可诱导转化生长因子-β(TGF-β)触发的信号传导,这与Aspn/PLAP-1对TGF-β的抑制作用一致。总之,这些结果表明,卵泡膜细胞可根据新的标志物基因及其生物学功能分为不同亚群,并提供证据表明Aspn/PLAP-1仅在卵泡膜细胞外层表达,并通过下调经典TGF-β信号级联在次级卵泡生长中起关键作用。