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Krüppel样因子4参与睾丸支持细胞的功能分化。

Krüppel-like factor 4 is involved in functional differentiation of testicular Sertoli cells.

作者信息

Godmann Maren, Katz Jonathan P, Guillou Florian, Simoni Manuela, Kaestner Klaus H, Behr Rüdiger

机构信息

Institute of Anatomy, Developmental Biology, University of Duisburg-Essen Medical School, 45122 Essen, Germany.

出版信息

Dev Biol. 2008 Mar 15;315(2):552-66. doi: 10.1016/j.ydbio.2007.12.018. Epub 2008 Feb 20.

Abstract

Krüppel-like factor 4 (KLF4) is a pleiotropic zinc finger transcription factor that regulates genes being involved in differentiation and cell-cycle control. Knockout studies revealed a critical function for KLF4 in the terminal differentiation of many epithelial cells. In testicular Sertoli cells, Klf4 is strongly inducible by the glycoprotein follicle stimulating hormone (FSH). Because KLF4 is essential for postnatal survival in mice, we deleted Klf4 specifically in Sertoli cells using the Cre/loxP system. Importantly, around postnatal day 18, a critical period of terminal Sertoli cell differentiation, mutant seminiferous tubules exhibited a disorganized germinal epithelium and delayed lumen formation. The ultrastructural finding of highly vacuolized Sertoli cell cytoplasm and the identification of differentially expressed genes, which are known to play roles during vesicle transport and fusion or for maintenance of the differentiated cell state, suggest impaired apical secretion of the Sertoli cell. Interestingly, a high proportion of all identified genes was localized in a small subregion of chromosome 7, suggesting coordinated regulation. Intriguingly, adult mutant mice are fertile and show normal testicular morphology, although the testosterone levels are decreased. In summary, KLF4 plays a significant role for proper and timely Sertoli cell differentiation in pubertal mice.

摘要

Krüppel样因子4(KLF4)是一种多效性锌指转录因子,可调节参与分化和细胞周期控制的基因。基因敲除研究揭示了KLF4在许多上皮细胞终末分化中的关键作用。在睾丸支持细胞中,Klf4可被糖蛋白促卵泡激素(FSH)强烈诱导。由于KLF4对小鼠出生后的存活至关重要,我们使用Cre/loxP系统在支持细胞中特异性删除了Klf4。重要的是,在出生后第18天左右,即支持细胞终末分化的关键时期,突变型生精小管的生精上皮出现紊乱,管腔形成延迟。支持细胞胞质高度空泡化的超微结构发现以及已知在囊泡运输和融合过程中发挥作用或维持分化细胞状态的差异表达基因的鉴定,提示支持细胞的顶端分泌受损。有趣的是,所有鉴定出的基因中有很大一部分位于7号染色体的一个小亚区域,提示存在协同调控。耐人寻味的是,成年突变小鼠虽然睾酮水平降低,但仍可育且睾丸形态正常。总之,KLF4在青春期小鼠支持细胞的正常及时分化中发挥着重要作用。

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