Protein tyrosine phosphorylation and protein tyrosine nitration in redox signaling

Protein tyrosine phosphorylation and protein tyrosine nitration in redox signaling

Autor Monteiro, Hugo P. Autor UNIFESP Google Scholar
Arai, Roberto J. Autor UNIFESP Google Scholar
Travassos, Luiz R. Autor UNIFESP Google Scholar
Instituição Universidade Federal de São Paulo (UNIFESP)
Resumo Reversible phosphorylation of protein tyrosine residues by polypeptide growth factor-receptor protein tyrosine kinases is implicated in the control of fundamental cellular processes including the cell cycle, cell adhesion, and cell survival, as well as cell proliferation and differentiation. During the last decade, it has become apparent that receptor protein tyrosine kinases and the signaling pathways they activate belong to a large signaling network. Such a network can be regulated by various extracellular cues, which include cell adhesion, agonists of G protein-coupled receptors, and oxidants. It is well documented that signaling initiated by receptor protein tyrosine kinases is directly dependent on the intracellular production of oxidants, including reactive oxygen and nitrogen species. Accumulated evidence indicates that the intracellular redox environment plays a major role in the mechanisms underlying the actions of growth factors. Oxidation of cysteine thiols and nitration of tyrosine residues on signaling proteins are described as posttranslational modifications that regulate, positively or negatively, protein tyrosine phosphorylation (PTP). Early observations described the inhibition of PTP activities by oxidants, resulting in increased levels of proteins phosphorylated on tyrosine. Therefore, a redox circuitry involving the increasing production of intracellular oxidants associated with growth-factor stimulation/cell adhesion, oxidative reversible inhibition of protein tyrosine phosphatases, and the activation of protein tyrosine kinases can be delineated.
Idioma Inglês
Data de publicação 2008-05-01
Publicado em Antioxidants & Redox Signaling. New Rochelle: Mary Ann Liebert Inc, v. 10, n. 5, p. 843-889, 2008.
ISSN 1523-0864 (Sherpa/Romeo, fator de impacto)
Publicador Mary Ann Liebert Inc
Extensão 843-889
Fonte http://dx.doi.org/10.1089/ars.2007.1853
Direito de acesso Acesso restrito
Tipo Resenha
Web of Science WOS:000254129600001
Endereço permanente http://repositorio.unifesp.br/handle/11600/30657

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