Exosomal miR-143-3p derived from follicular fluid promotes granulosa cell apoptosis by targeting BMPR1A in polycystic ovary syndrome

Abstract Polycystic ovary syndrome (PCOS) is an endocrine disorder that occurs in women of reproductive age. Anovulation caused by abnormal follicular development is still the main characteristic of PCOS patients with infertile. Granulosa cell (GC) is an important part of the follicular microenviron...

Full description

Bibliographic Details
Main Authors: Yuanyuan Zhao, Shuhong Pan, Yunying Li, Xiaohua Wu
Format: Article
Language:English
Published: Nature Portfolio 2022-03-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-022-08423-6
_version_ 1818321028177199104
author Yuanyuan Zhao
Shuhong Pan
Yunying Li
Xiaohua Wu
author_facet Yuanyuan Zhao
Shuhong Pan
Yunying Li
Xiaohua Wu
author_sort Yuanyuan Zhao
collection DOAJ
description Abstract Polycystic ovary syndrome (PCOS) is an endocrine disorder that occurs in women of reproductive age. Anovulation caused by abnormal follicular development is still the main characteristic of PCOS patients with infertile. Granulosa cell (GC) is an important part of the follicular microenvironment, the dysfunction of which can affect follicular development. Increasing evidence indicates that exosomal miRNAs derived from the follicular fluid (FF) of patients play critical roles during PCOS. However, which follicular fluid-derived exosomal miRNAs play a pivotal role in controlling granulosa cell function and consequently follicular development remain largely unknown, as does the underlying mechanism. Herein, we showed that miR-143-3p is highly expressed in the follicular fluid exosomes of patients with PCOS and can be delivered into granulosa cells. Furthermore, functional experiments showed that translocated miR-143-3p promoted granulosa cell apoptosis, which is important in follicle development. Mechanistically, BMPR1A was identified as a direct target of miR-143-3p. Overexpression of BMPR1A reversed the effects of exosomal miR-143-3p on GC apoptosis and proliferation by activating the Smad1/5/8 signaling pathway. These results demonstrate that miR-143-3p-containing exosomes derived from PCOS follicular fluid promoted granulosa cell apoptosis by targeting BMPR1A and blocking the Smad1/5/8 signaling pathway. Our findings provide a novel mechanism underlying the roles of exosomal-miRNAs in the follicular fluid of PCOS patients and facilitate the development of therapeutic strategies for PCOS.
first_indexed 2024-12-13T10:34:23Z
format Article
id doaj.art-f317d25061cd48e0ba615e305e4bdfc4
institution Directory Open Access Journal
issn 2045-2322
language English
last_indexed 2024-12-13T10:34:23Z
publishDate 2022-03-01
publisher Nature Portfolio
record_format Article
series Scientific Reports
spelling doaj.art-f317d25061cd48e0ba615e305e4bdfc42022-12-21T23:50:46ZengNature PortfolioScientific Reports2045-23222022-03-0112111210.1038/s41598-022-08423-6Exosomal miR-143-3p derived from follicular fluid promotes granulosa cell apoptosis by targeting BMPR1A in polycystic ovary syndromeYuanyuan Zhao0Shuhong Pan1Yunying Li2Xiaohua Wu3Center for Reproductive Medicine, The Fourth Hospital of Shijiazhuang (Gynecology and Obstetrics Hospital Affiliated to Hebei Medical University)Center for Reproductive Medicine, The Fourth Hospital of Shijiazhuang (Gynecology and Obstetrics Hospital Affiliated to Hebei Medical University)Center for Reproductive Medicine, The Fourth Hospital of Shijiazhuang (Gynecology and Obstetrics Hospital Affiliated to Hebei Medical University)Center for Reproductive Medicine, The Fourth Hospital of Shijiazhuang (Gynecology and Obstetrics Hospital Affiliated to Hebei Medical University)Abstract Polycystic ovary syndrome (PCOS) is an endocrine disorder that occurs in women of reproductive age. Anovulation caused by abnormal follicular development is still the main characteristic of PCOS patients with infertile. Granulosa cell (GC) is an important part of the follicular microenvironment, the dysfunction of which can affect follicular development. Increasing evidence indicates that exosomal miRNAs derived from the follicular fluid (FF) of patients play critical roles during PCOS. However, which follicular fluid-derived exosomal miRNAs play a pivotal role in controlling granulosa cell function and consequently follicular development remain largely unknown, as does the underlying mechanism. Herein, we showed that miR-143-3p is highly expressed in the follicular fluid exosomes of patients with PCOS and can be delivered into granulosa cells. Furthermore, functional experiments showed that translocated miR-143-3p promoted granulosa cell apoptosis, which is important in follicle development. Mechanistically, BMPR1A was identified as a direct target of miR-143-3p. Overexpression of BMPR1A reversed the effects of exosomal miR-143-3p on GC apoptosis and proliferation by activating the Smad1/5/8 signaling pathway. These results demonstrate that miR-143-3p-containing exosomes derived from PCOS follicular fluid promoted granulosa cell apoptosis by targeting BMPR1A and blocking the Smad1/5/8 signaling pathway. Our findings provide a novel mechanism underlying the roles of exosomal-miRNAs in the follicular fluid of PCOS patients and facilitate the development of therapeutic strategies for PCOS.https://doi.org/10.1038/s41598-022-08423-6
spellingShingle Yuanyuan Zhao
Shuhong Pan
Yunying Li
Xiaohua Wu
Exosomal miR-143-3p derived from follicular fluid promotes granulosa cell apoptosis by targeting BMPR1A in polycystic ovary syndrome
Scientific Reports
title Exosomal miR-143-3p derived from follicular fluid promotes granulosa cell apoptosis by targeting BMPR1A in polycystic ovary syndrome
title_full Exosomal miR-143-3p derived from follicular fluid promotes granulosa cell apoptosis by targeting BMPR1A in polycystic ovary syndrome
title_fullStr Exosomal miR-143-3p derived from follicular fluid promotes granulosa cell apoptosis by targeting BMPR1A in polycystic ovary syndrome
title_full_unstemmed Exosomal miR-143-3p derived from follicular fluid promotes granulosa cell apoptosis by targeting BMPR1A in polycystic ovary syndrome
title_short Exosomal miR-143-3p derived from follicular fluid promotes granulosa cell apoptosis by targeting BMPR1A in polycystic ovary syndrome
title_sort exosomal mir 143 3p derived from follicular fluid promotes granulosa cell apoptosis by targeting bmpr1a in polycystic ovary syndrome
url https://doi.org/10.1038/s41598-022-08423-6
work_keys_str_mv AT yuanyuanzhao exosomalmir1433pderivedfromfollicularfluidpromotesgranulosacellapoptosisbytargetingbmpr1ainpolycysticovarysyndrome
AT shuhongpan exosomalmir1433pderivedfromfollicularfluidpromotesgranulosacellapoptosisbytargetingbmpr1ainpolycysticovarysyndrome
AT yunyingli exosomalmir1433pderivedfromfollicularfluidpromotesgranulosacellapoptosisbytargetingbmpr1ainpolycysticovarysyndrome
AT xiaohuawu exosomalmir1433pderivedfromfollicularfluidpromotesgranulosacellapoptosisbytargetingbmpr1ainpolycysticovarysyndrome