Literature DB >> 20051481

Krüppel-like factor 4 is widely expressed in the mouse male and female reproductive tract and responds as an immediate early gene to activation of the protein kinase A in TM4 Sertoli cells.

M Godmann1, C Kosan, R Behr.   

Abstract

Krüppel-like factor 4 (KLF4) is a zinc finger transcription factor critically involved in cell proliferation, differentiation, and carcinogenesis. Recently, KLF4 has also been used for the generation of induced pluripotent stem cells. In this study, we analyzed Klf4 expression in different mouse tissues using northern blot analysis and immunohistochemistry. Focusing on the male and female reproductive tract, we showed for the first time that KLF4 is expressed in the epithelia of the murine uterus and the vagina. In the male reproductive tract, we detected KLF4 in the epithelia of the epididymis, ductus deferens, coagulating gland, and the penis. As KLF4 is strongly inducible by FSH signaling in Sertoli cells and as this transcription factor is also involved in Sertoli cell development, we employed the mouse Sertoli cell line TM4 as a model system to investigate i) the induction kinetics of Klf4 upon activation of the cAMP/protein kinase A pathway by forskolin and ii) the effects of Klf4 induction on TM4 cell cycle progression. Interestingly, Klf4 mRNA and protein were rapidly but transiently induced, reaching peak levels after 90-120 min and declining to basal levels within 4 h. Compared with the inducible cAMP early repressor, an immediate early response gene, the induction kinetics of Klf4 is much faster. In conclusion, Klf4 is an immediate early gene in TM4 cells and its expression in several epithelia of the male and female reproductive tract suggests an important role of Klf4 in mouse reproductive functions.

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Year:  2010        PMID: 20051481     DOI: 10.1530/REP-09-0531

Source DB:  PubMed          Journal:  Reproduction        ISSN: 1470-1626            Impact factor:   3.906


  14 in total

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Journal:  Gene       Date:  2017-02-22       Impact factor: 3.688

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Journal:  Cell Stem Cell       Date:  2020-04-02       Impact factor: 24.633

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Journal:  Age (Dordr)       Date:  2014-07-12

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Journal:  J Mol Biol       Date:  2013-04-29       Impact factor: 5.469

10.  Gs-coupled GPCR signalling in AgRP neurons triggers sustained increase in food intake.

Authors:  Ken-ichiro Nakajima; Zhenzhong Cui; Chia Li; Jaroslawna Meister; Yinghong Cui; Ou Fu; Adam S Smith; Shalini Jain; Bradford B Lowell; Michael J Krashes; Jürgen Wess
Journal:  Nat Commun       Date:  2016-01-08       Impact factor: 14.919

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