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Updated: Jun 4, 2026

A Seminiferous Tubule Squash Technique for the Cytological Analysis of Spermatogenesis Using the Mouse Model
Published on: February 6, 2018
CD147 is required for matrix metalloproteinases-2 production and germ cell migration during spermatogenesis
Hao Chen1, Kin Lam Fok, Sidney Yu
1Guangdong Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Shenzhen PKU-HKUST Medical Center, Shenzhen, PR China.
Abstract:
Spermatogenesis is a highly programmed process that requires the degradation of the extracellular matrix and the remodeling of tight junctions (TJ) to facilitate differentiating germ cell migration. Matrix metalloproteinases (MMPs) are essential in regulating Sertoli cell TJ in the testis. CD147 is known to stimulate the production of MMPs in tumor metastasis and its knockout mice are infertile. However, the functional relationship between CD147 and MMPs in spermatogenesis has not been investigated. In the present study, we examined the expression profile of CD147 and MMPs during mouse testicular development by RT-PCR, western blot and immunofluorescence staining. We also examined CD147 involvement in the production of MMP-2 and the migration of germ cells (GC-1 and GC-2 cells) using CD147 antibody or synthetic microRNA mimics-mediated knockdown. The results showed that CD147 was present at all stages of testicular development from 7 to 56 days post-partum (dpp). CD147 expression was found to increase after 21 days from moderate levels in 7 and 14 days. Of the eight MMPs studied, MMP-2, MMP-7, MMP-9 and MMP-23 were detected to have changes in expression during testicular development, with MMP-2 showing the largest change. CD147 and MMP-2 were co-localized in spermatogonia, spermatocytes and round spermatids in mouse testis, while in human testis, they were co-localized in spermatocytes and round spermatids. MMP-2 expression and migration of GC-1 and GC-2 cells were reduced by interfering with CD147 expression and function in vitro. These data suggest that CD147 regulates migration of spermatogonia and spermatocytes via induction of MMP-2 production during spermatogenesis.
Insights
CD147 protein regulates spermatogenesis by stimulating MMP-2 production, which is crucial for germ cell migration. This study investigates CD147
Area of Science:
- Reproductive biology and molecular endocrinology
- Cellular and molecular physiology
- Developmental biology
Background:
- Spermatogenesis involves extracellular matrix degradation and tight junction remodeling for germ cell migration.
- Matrix metalloproteinases (MMPs) are key regulators of Sertoli cell tight junctions.
- CD147's role in MMP production and its link to infertility warrant investigation in spermatogenesis.
Purpose of the Study:
- To investigate the functional relationship between CD147 and MMPs during mouse testicular development.
- To examine the expression profiles of CD147 and specific MMPs throughout spermatogenesis.
- To determine CD147's involvement in MMP-2 production and germ cell migration.
Main Methods:
- Real-time PCR (RT-PCR), Western blotting, and immunofluorescence staining were used to analyze CD147 and MMP expression.
- In vitro studies utilized CD147 antibody and microRNA mimics for knockdown experiments.
- Germ cell migration was assessed using GC-1 and GC-2 cell lines.
Main Results:
- CD147 expression was detected throughout testicular development, increasing after 21 days post-partum.
- MMP-2, MMP-7, MMP-9, and MMP-23 showed altered expression during testicular development, with MMP-2 exhibiting the most significant changes.
- CD147 and MMP-2 were co-localized in germ cells of both mouse and human testes.
- Interference with CD147 function in vitro reduced MMP-2 expression and germ cell migration.
Conclusions:
- CD147 plays a significant role in regulating spermatogenesis.
- CD147 likely controls spermatogonia and spermatocyte migration by inducing MMP-2 production.
- These findings highlight CD147 as a potential target for understanding male infertility.
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