Construction and evaluation of a cell model simulating the change of testicular microenvironment mediated by hypoxic and high-pressure conditions in varicocele mice.
- Author:
Shu-Lin LIANG
1
;
Li-Guo GENG
2
;
Ling HAN
1
;
Chu-Nan RONG
1
;
Zhan QIN
2
;
Juan DU
2
;
Chao-Ba HE
2
;
Shao-Ying YUAN
1
Author Information
1. The Second Clinical College, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong 510006, China.
2. Department of Andrology, Guangdong Hospital (Zhuhai Branch) of Traditional Chinese Medicine, Zhuhai, Guangdong 510915, China.
- Publication Type:Journal Article
- Keywords:
varicocele； infertility;
hypoxia;
high-pressure;
cell model;
testicular cells;
mice
- MeSH:
Male;
Animals;
Varicocele/pathology*;
Mice;
Testis/metabolism*;
Hypoxia-Inducible Factor 1, alpha Subunit/metabolism*;
Cell Hypoxia;
Cobalt;
Sertoli Cells/metabolism*;
Osmotic Pressure;
Spermatogenesis;
Cellular Microenvironment;
Infertility, Male;
Disease Models, Animal
- From:
National Journal of Andrology
2025;31(6):483-491
- CountryChina
- Language:Chinese
-
Abstract:
Objective： Varicocele (VC) induces male infertility by mediating changes in the testicular microenvironment, in which testicular hypoxia and high-pressure are important pathological conditions. This study aims to compare the mouse spermatogenesis (GC-2spd) cells and Sertoli (TM4) cells of mouse testis after hypoxic modeling and hypoxic and high-pressure combined modeling, and to explore the feasibility of establishing a hypoxic and high-pressure combined cell model. Methods： On the basis of cell hypoxia induced by CoCl2, the complex model of testicular cell hypoxia and high pressure was constructed by changing the osmotic pressure of GC-2 and TM4 cell medium with a high concentration of NaCl solution. After selecting the intervention concentration of CoCl2 by MTT test and detecting the expression level of HIF-1α for the determination of the optimal osmotic pressure conditions of the cell model, the cells were divided into normal group, hypoxia model group and composite model group. And the levels of OS, programmed cell death, inflammatory factors, and the expression levels of pyroptosis-related proteins were compared between the normal group and the groups with different modeling methods. Results： The optimal intervention concentration of CoCl2 in GC-2 and TM4 cells was 150 and 250μmol/L, respectively, and the expression of HIF-1α was the highest in both cells under osmotic pressure of 500 mOsmol/kg (P<0.05). Compared with the normal group, the SOD levels of GC-2 and TM4 cells decreased (all P<0.05), CAT level decreased (all P<0.05), and MDA level increased (all P<0.01), and the OS level of GC-2 and TM4 cells was more obvious than that of the hypoxia model group (all P<0.05). Compared with the normal group, apoptosis occurred in GC-2 and TM4 cells after composite modeling (all P<0.05). Compared with the normal group, the mRNA expressions of IL-1β, IL-18, TNF-α and COX-2 in GC-2 and TM4 cells significantly increased (P<0.01) and higher than those in hypoxia model group (P<0.05) and induced pyroptosis (P<0.01). The expression level of GSDMD increased (P<0.05). Conclusion： The cell model with hypoxia and high pressure combined modeling can not only induce oxidative stress and apoptosis of cells better than that with hypoxia alone, but also further cause inflammatory response damage and pyroptosis, which simulates the changes of testis microenvironment mediated by hypoxia and high pressure combined conditions in VC. This cell model can be used for studying the pathogenesis of VC-associated male infertility, evaluating drug efficacy, and exploring pharmacological mechanisms.
