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Promyelocytic leukaemia zinc finger protein (PLZF) is a glucocorticoid‐ and progesterone‐induced transcription factor in human endometrial stromal cells and myometrial smooth muscle cells

The promyelocytic leukaemia zinc finger (PLZF) protein belongs to the family of Krüppel‐like zinc finger proteins. It is a transcriptional repressor involved in cell cycle control and has been implicated in limb development, differentiation of myeloid cells, and spermatogenesis. Little is known abo...

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Bibliographic Details
Published in:Molecular human reproduction 2003-10, Vol.9 (10), p.611-623
Main Authors: Fahnenstich, Jasmin, Nandy, Andreas, Milde‐Langosch, Karin, Schneider‐Merck, Tanja, Walther, Norbert, Gellersen, Birgit
Format: Article
Language:English
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Summary:The promyelocytic leukaemia zinc finger (PLZF) protein belongs to the family of Krüppel‐like zinc finger proteins. It is a transcriptional repressor involved in cell cycle control and has been implicated in limb development, differentiation of myeloid cells, and spermatogenesis. Little is known about the regulation of PLZF expression. In search for mediators of progesterone signalling in the female reproductive tract, we discovered induction of PLZF mRNA in primary cultures of human endometrial stromal cells and myometrial smooth muscle cells (SMC) in response to progesterone. Surprisingly, dexamethasone was a more potent inducer of PLZF expression than progesterone and elicited a sustained up‐regulation of PLZF mRNA levels within 2 h. Immunofluorescence showed localization of PLZF to the nuclei of dexamethasone‐treated SMC. In uterine biopsies, nuclear staining for PLZF was found in myometrial cells and endometrial stromal cells of the secretory phase. The transcriptional start site of the PLZF gene was located to position –5801 in SMC. Transfected promoter constructs containing up to 4.1 kb of 5′‐flanking DNA were not induced by activated glucocorticoid or progesterone receptor. In contrast, co‐transfection of c‐jun and c‐fos expression vectors resulted in stimulation of reporter gene activity, indicating an involvement of AP‐1 transcription factors in PLZF expression.
ISSN:1360-9947
1460-2407
1460-2407
DOI:10.1093/molehr/gag080