4.5 Article

Glucose-induced production of hydrogen sulfide may protect the pancreatic beta-cells from apoptotic cell death by high glucose

Journal

FEBS LETTERS
Volume 583, Issue 2, Pages 377-382

Publisher

WILEY
DOI: 10.1016/j.febslet.2008.12.026

Keywords

Hydrogen sulfide; Pancreatic beta-cell; Cystathionine-gamma-lyase (CSE); Cystathionine-beta-synthase (CBS); Apoptosis; L-Cysteine

Funding

  1. Japan Society Promotion of Science [19591060]
  2. Oita Broadcasting System Cultural Foundation
  3. Oita University Venture Business Laboratory
  4. Grants-in-Aid for Scientific Research [21790154, 19591060] Funding Source: KAKEN

Ask authors/readers for more resources

We examined the expression of the major H2S-producing enzymes, cystathionine-beta-synthase (CBS) and cystathionine-gamma-lyase (CSE). CBS was ubiquitously distributed in the mouse pancreas, but CSE was found only in the exocrine. Freshly isolated islets expressed CBS, while CSE was faint. However, high glucose increased the CSE expression in the beta-cells. L-Cysteine or NaHS suppressed islet cell apoptosis with high glucose, and increased glutathione content in MIN6 beta-cells. Pretreatment with L-cysteine improved the secretory responsiveness following stimulation with glucose. The CSE inhibitor DL-propargylglycine antagonized these L-cysteine effects. We suggest H2S may function as an 'intrinsic brake' which protects beta-cells from glucotoxicity. (C) 2008 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.

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