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Updated: Aug 2, 2025

A Tissue Culture Model of Estrogen-producing Primary Bovine Granulosa Cells
Published on: September 6, 2018
MiR-145 regulates steroidogenesis in mouse primary granulosa cells by targeting Arpc5 and subsequent cytoskeleton
Lanfang Ma1, Shuo Wang2, Jun Yang3
1Department of Obstetrics and Gynecology, Guiyang Maternity and Child Health Care Hospital, Guizhou 550003, People's Republic of China.
Abstract:
MicroRNA (miR)-145 is enriched in the follicular granulosa cells (GCs) of 3-week-old mice. Downregulating miR-145 inhibits the proliferation and differentiation of GCs and induces evident changes in their cytoskeleton. In this study, we examined how miR-145 induces cytoskeletal changes in mouse GCs and its potential mechanism in regulating GC steroidogenesis. We found that actin related protein 2/3 complex subunit 5 (Arpc5) is a target of miR-145. The miR-145 antagomir increased ARPC5 expression but not β-ACTIN, β-TUBULIN, and PAXILLIN expression. Arpc5 overexpression inhibited GC proliferation, differentiation, and progesterone synthesis. Furthermore, the expression of progesterone synthesis-associated enzymes was downregulated in the Arpc5 overexpression group, and the GC cytoskeleton exhibited evident changes. We conclude that Arpc5, a new target of miR-145, regulates primary GC proliferation and progesterone production by regulating the cytoskeleton remodeling.
Insights
MicroRNA-145 (miR-145) targets actin-related protein 5 (Arpc5) in mouse granulosa cells. Arpc5 regulates cell proliferation, differentiation, and progesterone production via cytoskeleton remodeling.
Area of Science:
- Reproductive Biology
- Molecular Endocrinology
- Cell Biology
Background:
- MicroRNA-145 (miR-145) is abundant in mouse follicular granulosa cells (GCs).
- Downregulation of miR-145 impairs GC proliferation, differentiation, and alters cytoskeleton structure.
Purpose of the Study:
- To investigate the mechanism by which miR-145 influences GC cytoskeleton.
- To determine miR-145's role in regulating GC steroidogenesis.
Main Methods:
- Quantitative real-time PCR and Western blotting to assess gene and protein expression.
- Overexpression and knockdown studies of miR-145 and its target Arpc5 in GCs.
- Assessment of GC proliferation, differentiation markers, and progesterone synthesis.
Main Results:
- Actin-related protein 2/3 complex subunit 5 (Arpc5) was identified as a direct target of miR-145.
- Arpc5 overexpression mimicked the effects of miR-145 downregulation, inhibiting GC proliferation, differentiation, and progesterone synthesis.
- Arpc5 overexpression led to significant alterations in the GC cytoskeleton and downregulated key steroidogenic enzymes.
Conclusions:
- Arpc5 is a novel target of miR-145 that plays a crucial role in regulating granulosa cell proliferation and progesterone production.
- miR-145/Arpc5 axis impacts GC function through modulation of cytoskeleton remodeling and steroidogenesis.
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