Abstract

Circular RNAs (circRNAs) are thought to play essential roles in multiple biological processes, including apoptosis, an important process in antral follicle atresia. We aimed to investigate the potential involvement of circRNAs in granulosa cell apoptosis and thus antral follicle atresia. CircRNA expression profiles were generated from porcine granulosa cells isolated from healthy antral (HA) and atretic antral (AA) follicles. Over 9632 circRNAs were identified, of which 62 circRNAs were differentially expressed (DE-circRNAs). Back-splicing, RNase R resistance, and stability of DE-circRNAs were validated, and miRNA binding sites and related target genes were predicted. Two exonic circRNAs with low false discovery rate (FDR) high fold change, miRNA binding sites, and relevant biological functions—circ_CBFA2T2 and circ_KIF16B—were selected for further characterization. qRT-PCR and linear regression analysis confirmed expression and correlation of the targeted genes—the antioxidant gene GCLC (potential target of circ_CBFA2T2) and the apoptotic gene TP53 (potential target of circ_KIF16B). Increased mRNA content of TP53 in granulosa cells of AA follicles was further confirmed by strong immunostaining of both p53 and its downstream target pleckstrin homology like domain family a member 3 (PHLDA3) in AA follicles compared to negligible staining in granulosa cells of HA follicles. Therefore, we concluded that aberrantly expressed circRNAs presumably play a potential role in antral follicular atresia.

Highlights

  • Each estrous cycle, a cohort of small antral follicles in, is recruited to enter the pool of growing antral follicles

  • Misotl.oSlcoi.g2i0c2a0l, 2a1n, d521H7ormone Characteristics between Healthy Antral (HA) and Atretic Antra3l of 25 (AA) Follicles ovarIiannatnistrsaulef,owlleicclehsowseittho ausweethlle-vpaisgcuaslaarnizaendimfoalllicmuoladrewl taollinavnedstcilgeaatreftohlleicruollearoffluciirdc,RtNheAcseilnlsafnrotrmal tfhoelligcrualnarulaotsreasilaa.yeFrorwtherise ptiugrhptolysea, dthheerfeedatutoreesaocfhciortchReNr,Ains dinicpaotirvceinoefgarahneuallothsaycaenlltsradlerfoivlleidclefr.oImn fhoellailctlheys wanitdhaatrpeotiocralyntvraasl cfuolllaircilzeesdwfeorlelicsutuladriewdaullsainngdRaNraAth-seerqo, pfoalqlouwe eadppbeyaqraRnTc-eP,CthReingrcaonmulboisnaatcieolnl lwayitehr cwircaRs NdAis-omrgiRanNizAe-dm, RaNndA nneutmweorrokucsonasptorupctotitoicn acneldlsvawliedraetiponre.sent; in some cases, apoptotic g2r.aRneusluosltas cells were found to be dispersed throughout the antrum, indicative of follicular degeneration

  • We showed that the p53/PHLDA3 pathway might participate in granulosa cell apoptosis

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Summary

Introduction

A cohort of small antral follicles in, is recruited to enter the pool of growing antral follicles. From this pool, dominant follicles are selected by a process highly dependent on follicle-stimulating hormone (FSH) [1,2]. Granulosa cell death by apoptosis is the main cause of antral follicular atresia [5]. Initiation of granulosa apoptosis can be triggered by extrinsic factors, such as inflammation, and intrinsic factors, such as oxidative stress [6]. The underlying regulatory mechanism, which determines whether granulosa cells of selected antral follicles will undergo apoptosis, is still not fully characterized

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