Your browser doesn't support javascript.
loading
The modulation of the phosphorylation status of NKCC1 in organ cultured bovine lenses: Implications for the regulation of fiber cell and overall lens volume.
Vorontsova, Irene; Donaldson, Paul J; Kong, Zhiying; Wickremesinghe, Chiharu; Lam, Leo; Lim, Julie C.
Afiliação
  • Vorontsova I; Department of Physiology, School of Medical Sciences, New Zealand National Eye Centre, The University of Auckland, New Zealand; Department of Physiology and Biophysics, Department of Developmental and Cell Biology, University of California, Irvine, CA, USA.
  • Donaldson PJ; Department of Physiology, School of Medical Sciences, New Zealand National Eye Centre, The University of Auckland, New Zealand.
  • Kong Z; Department of Physiology, School of Medical Sciences, New Zealand National Eye Centre, The University of Auckland, New Zealand.
  • Wickremesinghe C; Department of Physiology, School of Medical Sciences, New Zealand National Eye Centre, The University of Auckland, New Zealand.
  • Lam L; Department of Physiology, School of Medical Sciences, New Zealand National Eye Centre, The University of Auckland, New Zealand.
  • Lim JC; Department of Physiology, School of Medical Sciences, New Zealand National Eye Centre, The University of Auckland, New Zealand. Electronic address: j.lim@auckland.ac.nz.
Exp Eye Res ; 165: 164-174, 2017 12.
Article em En | MEDLINE | ID: mdl-28818393
ABSTRACT
In previous work, we have shown the Sodium/Potassium/2 Chloride Cotransporter (NKCC1) to be a key effector of lens fiber cell volume regulation. Since others have shown that the activity of NKCC1 is regulated via its phosphorylation status, the purpose of this study was to investigate whether NKCC1 phosphorylation can be modulated in organ cultured bovine lenses, and to see how this relates to changes in lens wet weight. Western blotting was first used to confirm the expression of NKCC1, phosphorylated NKCC1 (NKCC1-P) and the regulatory kinases WNK/SPAK and phosphatases PP1/PP2A in bovine lenses at the protein level. Changes to NKCC1-P status were then assessed by organ culturing bovine lenses in either isotonic, hypertonic or hypotonic solutions in the presence or absence of the NKCC inhibitor, bumetanide, or phosphatase inhibitors okadaic acid and calyculin A. After 1-22 h of culturing, lenses were weighed, assessed for transparency and the cortical protein fractions analyzed by western blot using antibodies to detect total NKCC1 and NKCC1-P. NKCC1, NKCC1-P, SPAK, PP1 and PP2A were all detected in the membrane fraction of bovine lenses. Under hypertonic conditions, NKCC1 is phosphorylated and activated to mediate a regulatory volume increase. Finally, NKCC1-P signal increased in the presence of phosphatase inhibitors indicating that PP1/PP2A can dephosphorylate NKCC1. These results show that the phosphorylation status and hence activity of NKCC1 is dynamically regulated and that in response to hypertonic stress, NKCC1 activity is increased to effect a regulatory volume increase that limits cell shrinkage. These findings support the view that the lens dynamically regulates ion fluxes to maintain steady state lens volume, and suggest that dysfunction of this regulation maybe an initiating factor in the localized fiber cell swelling that is a characteristic of diabetic lens cataract.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Membro 2 da Família 12 de Carreador de Soluto / Cristalino Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Exp Eye Res Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Membro 2 da Família 12 de Carreador de Soluto / Cristalino Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Exp Eye Res Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos