Proliferation of adult Sertoli cells following conditional knockout of the gap junctional protein GJA1 (Connexin 43) in mice

被引:182
作者
Sridharan, Santhi
Simon, Liz
Meling, Daryl D.
Cyr, Daniel G.
Gutstein, David E.
Fishman, Glenn I.
Guillou, Florian
Cooke, Paul S.
机构
[1] Univ Illinois, Dept Vet Biosci, Urbana, IL 61802 USA
[2] Univ Quebec, Inst Natl Rech Sci Sante, Pointe Claire, PQ H9R 1G6, Canada
[3] NYU, Sch Med, Leon H Charney Div Cardiol, New York, NY 10016 USA
[4] Univ Tours, CNRS, INRA, UMR 6175, F-37380 Nouzilly, France
关键词
cytokines; gamete biology; Sertoli cell differentiation and proliferation; spermatogenesis; spermatogonia; testis;
D O I
10.1095/biolreprod.106.059212
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
GJA1 (also known and referred to here as connexin 43 and abbreviated CX43) is the predominant testicular gap junction protein, and CX43 may regulate Sertoli cell maturation and spermatogenesis. We hypothesized that lack of CX43 would inhibit Sertoli cell differentiation and extend proliferation. To test this, a Sertoli cell-specific Cx43 knockout (SC-Cx43 KO) mouse was generated using Cre-lox technology. Immunohistochemistry indicated that CX43 was not expressed in the Sertoli cells of SC-Cx43 KO mice, but was normal in organs such as the heart. Testicular weight was reduced by 41% and 76% in SC-Cx43 KO mice at 20 and 60 days, respectively, vs. wild-type (wt) mice. Seminiferous tubules of SC-Cx43 KO mice contained only Sertoli cells and actively proliferating early spermatogonia. Sertoli cells normally cease proliferation at 2 wk of age in mice and become terminally differentiated. However, proliferating Sertoli cells were present in SC-Cx43 KO but not wt mice at 20 and 60 days of age. Thyroid hormone receptor alpha (THRA) is high in proliferating Sertoli cells, then declines sharply in adulthood. Thra mRNA expression was increased in 20-day SCCx43 KO vs. wt mice, and it showed a trend toward an increase in 60-day mice, indicating that loss of CX43 in Sertoli cells inhibited their maturation. In conclusion, we have generated mice lacking CX43 in Sertoli cells but not other tissues. Our data indicate that CX43 in Sertoli cells is essential for spermatogenesis but not spermatogonial maintenance/proliferation. SC-Cx43 KO mice showed continued Sertoli cell proliferation and delayed maturation in adulthood, indicating that CX43 plays key roles in Sertoli cell development.
引用
收藏
页码:804 / 812
页数:9
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