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Updated: Jul 8, 2025

Author Spotlight: Investigating the Mechanisms and Inducing Models of Polycystic Ovary Syndrome
Published on: July 5, 2024
Reduced PATL2 Impairs the Proliferation of Ovarian Granulosa Cells by Decreasing ADM2 Expression in Patients with
Jun Tan1,2, Pei-Pei Liu3,4, Li-Yun Cao3,4
1Reproductive Medicine Center, Jiangxi Maternal and Child Health Hospital, No. 318, Bayi Avenue, Donghu District, Nanchang, Jiangxi Province, China. tanjun561127@163.com.
Abstract:
It is recognized that PCOS patients are often accompanied with aberrant follicular development, which is an important factor leading to infertility in patients. However, the relevant regulatory mechanisms of abnormal follicular development are not well understood. In the present study, by collecting human ovarian granulosa cells (GCs) from PCOS patients who underwent in vitro fertilization (IVF), we found that the proliferation ability of GCs in PCOS patients was significantly reduced. Surprisingly, PATL2 and adrenomedullin 2 (ADM2) were obviously decreased in the GCs of PCOS patients. To further explore the potential roles of PATL2 and ADM2 on GC, we transfected PATL2 siRNA into KGN cells to knock down the expression of PATL2. The results showed that the growth of GCs remarkably repressed after knocking down the PATL2, and ADM2 expression was also weakened. Subsequently, to study the relationship between PATL2 and ADM2, we constructed PATL2 mutant plasmid lacking the PAT construct and transfected it into KGN cells. The cells showed the normal PATL2 expression, but attenuated ADM2 expression and impaired proliferative ability of GCs. Finally, the rat PCOS model experiments further confirmed our findings in KGN cells. In conclusion, our study suggests that PATL2 promoted the proliferation of ovarian GCs by stabilizing the expression of ADM2 through "PAT" structure, which is beneficial to follicular development, whereas, in the ovary with polycystic lesions, reduction of PATL2 could result in the decreased expression of ADM2, subsequently weakened the proliferation ability of GCs and finally led to the occurrence of aberrant follicles.
Insights
Polycystic ovary syndrome (PCOS) impairs ovarian granulosa cell (GC) proliferation due to reduced PATL2, which stabilizes adrenomedullin 2 (ADM2). This leads to aberrant follicular development and infertility in PCOS patients.
Area of Science:
- Reproductive biology
- Cellular and molecular endocrinology
Background:
- Polycystic ovary syndrome (PCOS) is linked to aberrant follicular development and infertility.
- The regulatory mechanisms underlying abnormal follicular development in PCOS remain poorly understood.
Purpose of the Study:
- To investigate the roles of PATL2 and adrenomedullin 2 (ADM2) in the proliferation of ovarian granulosa cells (GCs) from PCOS patients.
- To elucidate the mechanism by which PATL2 influences GC proliferation and ADM2 expression.
Main Methods:
- Collected human ovarian granulosa cells (GCs) from PCOS patients undergoing in vitro fertilization (IVF).
- Utilized siRNA to knock down PATL2 expression in KGN cells (a GC line).
- Constructed and transfected a PATL2 mutant plasmid into KGN cells.
- Performed experiments on a rat PCOS model.
Main Results:
- GCs from PCOS patients exhibited significantly reduced proliferation ability.
- PATL2 and ADM2 expression were decreased in GCs from PCOS patients.
- Knocking down PATL2 in KGN cells repressed GC growth and weakened ADM2 expression.
- A PATL2 mutant lacking the "PAT" structure attenuated ADM2 expression and impaired GC proliferation.
Conclusions:
- PATL2 promotes ovarian GC proliferation by stabilizing ADM2 expression via its "PAT" structure, supporting follicular development.
- Reduced PATL2 in PCOS ovaries leads to decreased ADM2 expression, impaired GC proliferation, and aberrant follicle formation.
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