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Kwon, Hyug Moo
Immunometabolism and Cancer Lab.
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Tonicity-independent regulation of the osmosensitive transcription factor TonEBP (NFAT5)

Author(s)
Halterman, Julia A.Kwon, H. MooWamhoff, Brian R.
Issued Date
2012-01
DOI
10.1152/ajpcell.00327.2011
URI
https://scholarworks.unist.ac.kr/handle/201301/4681
Fulltext
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=83455176314
Citation
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, v.302, no.1, pp.C1 - C8
Abstract
Halterman JA, Kwon HM, Wamhoff BR. Tonicity-independent regulation of the osmosensitive transcription factor TonEBP (NFAT5). Am J Physiol Cell Physiol 302: C1-C8, 2012. First published October 12, 2011; doi:10.1152/ajpcell.00327.2011.-Tonicity-responsive enhancer binding protein (TonEBP/nuclear factor of activated T-cells 5 [NFAT5]) is a Rel homology transcription factor classically known for its osmosensitive role in regulating cellular homeostasis during states of hypo-and hypertonic stress. A recently growing body of research indicates that TonEBP is not solely regulated by tonicity, but that it can be stimulated by various tonicity-independent mechanisms in both hypertonic and isotonic tissues. Physiological and pathophysiological stimuli such as cytokines, growth factors, receptor and integrin activation, contractile agonists, ions, and reactive oxygen species have been implicated in the positive regulation of TonEBP expression and activity in diverse cell types. These new data demonstrate that tonicity-independent stimulation of TonEBP is critical for tissue-specific functions like enhanced cell survival, migration, proliferation, vascular remodeling, carcinoma invasion, and angiogenesis. Continuing research will provide a better understanding as to how these and other alternative TonEBP stimuli regulate gene expression in both health and disease.
Publisher
AMER PHYSIOLOGICAL SOC
ISSN
0363-6143
Keyword (Author)
nuclear factor of activated T-cells 5gene expressionosmotic stress
Keyword
ENHANCER-BINDING PROTEINNUCLEUS PULPOSUS CELLSOXYGEN SPECIES CONTRIBUTEINTERVERTEBRAL DISC CELLSNACL-INDUCED ACTIVATIONOSMOTIC-STRESSRHEUMATOID-ARTHRITISOSMOPROTECTIVE GENESNITRIC-OXIDEARTICULAR-CARTILAGE

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