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维生素D通过抑制NLRP3来保护精原细胞和支持细胞免受热应激损伤。

Vitamin D protects spermatogonia and Sertoli cells from heat stress damage by inhibiting NLRP3.

作者信息

Chu Han, Deng Qi-Fei, Fang Yuan

机构信息

The Department of Pediatric Urology Surgery, Anhui Provincial Children's Hospital, Hefei, Anhui, China.

Pathology Department, Anhui Provincial Children's Hospital, Hefei, Anhui, China.

出版信息

Front Pediatr. 2025 Jan 7;12:1495310. doi: 10.3389/fped.2024.1495310. eCollection 2024.

Abstract

INTRODUCTION

Cryptorchidism can damage cells in the cryptorchid testes due to elevated local temperatures, potentially impacting the fertility of the child in adulthood. Research indicates that vitamin D enhances sperm quality in adult males. This study aimed to explore whether vitamin D inhibits NLRP3 activation, thus helping to mitigate heat stress damage to testicular spermatogenic and Sertoli cells.

MATERIALS AND METHODS

Five cases of normal testicular tissue adjacent to a tumor (testis removed due to tumorous growth) and five cases of atrophied cryptorchid testicular tissue (testis removed) were analyzed for immunohistochemistry to determine NLRP3 expression in cryptorchid tissue. In Phase I, spermatogonia (GC-1) and Sertoli cells (TM4) were separated into blank and heat stress groups. Apoptosis, inflammatory factor levels, and the expression of Bcl-2 and NLRP3 genes and proteins were measured at 2, 6, and 10 h after heat stress treatment. In Phase II, the cells were re-cultured and divided into three groups: heat stress, siRNA + heat stress, and VD + heat stress. After 10 h, the apoptosis, inflammatory factor levels, and gene and protein expressions of Bcl-2 and NLRP3 were reassessed in each group.

RESULTS

Immunohistochemistry indicated NLRP3 expression in cryptorchid tissue. Phase I, extending heat stress duration led to increased apoptosis in spermatogonia (GC-1) and testicular Sertoli cells (TM4), heightened levels of inflammatory factors, reduced BCL-2 expression, and elevated NLRP3 expression compared to the control group. Phase II, both the siRNA + heat stress and VD + heat stress groups showed decreased apoptosis in spermatogonia and Sertoli cells, lower inflammatory factor levels, increased BCL-2 expression, and decreased NLRP3 expression compared to the heat stress-only group, with statistically significant differences ( < 0.05).

CONCLUSIONS

This is the first time we found the expression of NLRP3 in cryptorchidism. Vitamin D can inhibit the expression of NLRP3 and reduce the damage of heat stress on testicular spermatogenic cells and Sertoli cells, and play a protective role for testicular spermatogenic cells and Sertoli cells. This provides a theoretical basis for preserving testicular function during the "treatment gap" in boys with cryptorchidism who have not received surgical treatment.

摘要

引言

隐睾症可因局部温度升高而损害隐睾中的细胞,这可能会影响孩子成年后的生育能力。研究表明,维生素D可提高成年男性的精子质量。本研究旨在探讨维生素D是否能抑制NLRP3激活,从而有助于减轻热应激对睾丸生精细胞和支持细胞的损伤。

材料与方法

对5例肿瘤旁正常睾丸组织(因肿瘤生长而切除的睾丸)和5例萎缩性隐睾睾丸组织(切除的睾丸)进行免疫组织化学分析,以确定隐睾组织中NLRP3的表达。在第一阶段,将精原细胞(GC-1)和支持细胞(TM4)分为空白组和热应激组。在热应激处理后2、6和10小时测量细胞凋亡、炎症因子水平以及Bcl-2和NLRP3基因与蛋白的表达。在第二阶段,将细胞重新培养并分为三组:热应激组、siRNA+热应激组和VD+热应激组。10小时后,重新评估每组细胞的凋亡、炎症因子水平以及Bcl-2和NLRP3的基因与蛋白表达。

结果

免疫组织化学显示隐睾组织中有NLRP3表达。第一阶段,与对照组相比,延长热应激持续时间导致精原细胞(GC-1)和睾丸支持细胞(TM4)凋亡增加、炎症因子水平升高、BCL-2表达降低以及NLRP3表达升高。第二阶段,与仅热应激组相比,siRNA+热应激组和VD+热应激组的精原细胞和支持细胞凋亡均减少、炎症因子水平降低、BCL-2表达增加以及NLRP3表达降低,差异具有统计学意义(<0.05)。

结论

这是我们首次发现NLRP3在隐睾症中的表达。维生素D可抑制NLRP3的表达,减轻热应激对睾丸生精细胞和支持细胞的损伤,对睾丸生精细胞和支持细胞起到保护作用。这为未接受手术治疗的隐睾症男孩在“治疗间隙”期间保留睾丸功能提供了理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df39/11747411/d980b9538c84/fped-12-1495310-g001.jpg

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