Literature DB >> 9398602

Cardiac expressions of HIF-1 alpha and HLF/EPAS, two basic loop helix/PAS domain transcription factors involved in adaptative responses to hypoxic stresses.

A Ladoux1, C Frelin.   

Abstract

Expression of many mammalian genes is regulated by oxygen tension. HIF-1 alpha and HLF/EPAS are two basic helix-loop-helix/PAS domain transcription factors that bind to hypoxia sensitive elements in the promoters /enhancers of hypoxia sensitive genes such as vascular endothelial growth factor (VEGF). This paper describes the structure of rat HIF-1 alpha and analyses expressions HIF-1 alpha and of HLF/EPAS mRNAs in lung and cardiac tissues from the rat. HLF/EPAS mRNAs appear at birth in the two tissues and are maintained at high levels throughout adult life. HIF-1 alpha mRNAs are expressed at a constant level during lung development. Their abundance increase transiently at birth in cardiac tissues. Cultured cardiomyocytes from new born rats only express HIF-1 alpha mRNAs. HIF-1 alpha mRNA expression is increased by phorbol myristate acetate but not by anoxia or cobalt. The results indicate (i) that HIF-1 alpha and HLF/EPAS are expressed in a cell specific manner and (ii) that the hypoxic induction of VEGF mRNA expression by isolated cardiomyocytes is independent of HLF/EPAS. Finally, they suggest that protein kinase C may prime hypoxia induced gene regulation by inducing expression of HIF-1 alpha mRNAs.

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Year:  1997        PMID: 9398602     DOI: 10.1006/bbrc.1997.7708

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  12 in total

1.  Perivenous expression of the mRNA of the three hypoxia-inducible factor alpha-subunits, HIF1alpha, HIF2alpha and HIF3alpha, in rat liver.

Authors:  T Kietzmann; Y Cornesse; K Brechtel; S Modaressi; K Jungermann
Journal:  Biochem J       Date:  2001-03-15       Impact factor: 3.857

2.  Regulation of endothelin-1 gene expression in human microvascular endothelial cells by hypoxia and cobalt: role of hypoxia responsive element.

Authors:  A Minchenko; J Caro
Journal:  Mol Cell Biochem       Date:  2000-05       Impact factor: 3.396

Review 3.  Natural product-derived small molecule activators of hypoxia-inducible factor-1 (HIF-1).

Authors:  Dale G Nagle; Yu-Dong Zhou
Journal:  Curr Pharm Des       Date:  2006       Impact factor: 3.116

Review 4.  Hypoxia and fetal heart development.

Authors:  A J Patterson; L Zhang
Journal:  Curr Mol Med       Date:  2010-10       Impact factor: 2.222

Review 5.  Vasotrophic regulation of age-dependent hypoxic cerebrovascular remodeling.

Authors:  Jinjutha Silpanisong; William J Pearce
Journal:  Curr Vasc Pharmacol       Date:  2013-09       Impact factor: 2.719

6.  Targeting HIF-α for robust prevascularization of human cardiac organoids.

Authors:  Robert C Coyle; Ryan W Barrs; Dylan J Richards; Emma P Ladd; Donald R Menick; Ying Mei
Journal:  J Tissue Eng Regen Med       Date:  2020-12-08       Impact factor: 3.963

7.  Oxygen Sensing, Cardiac Ischemia, HIF-1α and Some Emerging Concepts.

Authors:  Shyamal K Goswami; Dipak K Das
Journal:  Curr Cardiol Rev       Date:  2010-11

8.  Skeletal muscle HIF-1alpha expression is dependent on muscle fiber type.

Authors:  Didier F Pisani; Claude A Dechesne
Journal:  J Gen Physiol       Date:  2005-08       Impact factor: 4.086

9.  Prognostic Role of Hypoxia-Inducible Factor-2α Tumor Cell Expression in Cancer Patients: A Meta-Analysis.

Authors:  Eloy Moreno Roig; Ala Yaromina; Ruud Houben; Arjan J Groot; Ludwig Dubois; Marc Vooijs
Journal:  Front Oncol       Date:  2018-06-11       Impact factor: 6.244

10.  RhoA regulation of cardiomyocyte differentiation.

Authors:  Mari Kaarbø; Denis I Crane; Wayne G Murrell
Journal:  ScientificWorldJournal       Date:  2013-06-27
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