Literature DB >> 10072529

NF-ATc isoforms are differentially expressed and regulated in murine T and mast cells.

M A Sherman1, D R Powell, D L Weiss, M A Brown.   

Abstract

NF of activated T cells (NF-AT) denotes a family of transcription factors that regulate the activation-dependent expression of many immunologically important proteins. At least four distinct genes encode the various family members, and several isoforms of these have been identified as well. The overlapping expression patterns and similar in vitro binding and trans-activation activities on various promoter elements of NF-AT-regulated genes suggest some redundancy in the function of these proteins. However, the phenotypic analysis of NF-AT-deficient mice supports the idea that there are tissue- and gene-specific functions as well. In this study we have characterized the expression of NF-AT cDNAs in murine mast cells. The majority of clones identified correspond to two NF-ATc isoforms that differ only in their amino-terminal sequence. Despite minimal discrepancies in the coding region, there are striking tissue- and cell type-specific differences in isoform expression patterns. Detection of NF-ATc.alpha mRNA is strictly dependent on cell activation signals in both T and mast cell lines. In contrast, the beta isoform is expressed at very low constitutive levels in both cell types but is only up-regulated in response to mast cell activation signals delivered through the FcepsilonRI or via calcium ionophores. These results demonstrate another level of regulation within the NF-AT family that can contribute to cell type-specific gene expression.

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Year:  1999        PMID: 10072529

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  5 in total

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Authors:  Pedro I Lucena; Douglas V Faget; Emilia Pachulec; Marcela C Robaina; Claudete E Klumb; Bruno K Robbs; João P B Viola
Journal:  Mol Cell Biol       Date:  2015-10-19       Impact factor: 4.272

2.  Interferon regulatory factor 2 binding protein 2 is a new NFAT1 partner and represses its transcriptional activity.

Authors:  Flávia R G Carneiro; Renata Ramalho-Oliveira; Giuliana P Mognol; João P B Viola
Journal:  Mol Cell Biol       Date:  2011-05-16       Impact factor: 4.272

3.  c-Jun NH(2)-terminal kinase inhibits targeting of the protein phosphatase calcineurin to NFATc1.

Authors:  C W Chow; C Dong; R A Flavell; R J Davis
Journal:  Mol Cell Biol       Date:  2000-07       Impact factor: 4.272

4.  Interleukin-10 inhibits osteoclastogenesis by reducing NFATc1 expression and preventing its translocation to the nucleus.

Authors:  Kathryn E Evans; Simon W Fox
Journal:  BMC Cell Biol       Date:  2007-01-19       Impact factor: 4.241

5.  Polyoma virus-induced osteosarcomas in inbred strains of mice: host determinants of metastasis.

Authors:  Palanivel Velupillai; Chang Kyoo Sung; Yu Tian; Jean Dahl; John Carroll; Roderick Bronson; Thomas Benjamin
Journal:  PLoS Pathog       Date:  2010-01-22       Impact factor: 6.823

  5 in total

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