4.3 Article

The lipocalin alpha(1)-microglobulin protects erythroid K562 cells against oxidative damage induced by heme and reactive oxygen species

期刊

FREE RADICAL RESEARCH
卷 42, 期 8, 页码 725-736

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/10715760802337265

关键词

antioxidation; alpha(1)-microglobulin; red cell; ROS; heme

资金

  1. Swedish Research Council [2005-7144, 2005-6582]
  2. King Gustav V's 80-year Foundation
  3. Swedish Society for Medical Research, the Royal Physiographic Society in Lund
  4. Foundations of Greta and Johan Kock and Alfred Osterlund
  5. Swedish Foundation for International Cooperation in Research and Higher Education (STINT)
  6. Blood and Defence Network
  7. Lund University
  8. Crafoord Foundation
  9. Thelma Zoega Foundation

向作者/读者索取更多资源

alpha(1)-Microglobulin is a 26 kDa plasma and tissue glycoprotein that belongs to the lipocalin protein superfamily. Recent reports show that it is a reductase and radical scavenger and that it binds heme and has heme-degrading properties. This study has investigated the protective effects of alpha(1)-microglobulin against oxidation by heme and reactive oxygen species in the human erythroid cell line, K562. The results show that alpha(1)-microglobulin prevents intracellular oxidation and up-regulation of heme oxygenase-1 induced by heme, hydrogen peroxide and Fenton reaction-generated hydroxyl radicals in the culture medium. It also reduces the cytosol of non-oxidized cells. Endogeneous expression of alpha(1)-microglobulin was up-regulated by these oxidants and silencing of the alpha(1)-microglobulin expression increased the cytosol oxidation. alpha(1)-microglobulin also inhibited cell death caused by heme and cleared cells from bound heme. Binding of heme to alpha(1)-microglobulin increased the radical reductase activity of the protein as compared to the apo-protein. Finally, alpha(1)-microglobulin was localized mainly at the cell surface both when administered exogeneously and in non-treated cells. The results suggest that alpha(1)-microglobulin is involved in the defence against oxidative cellular injury caused by haemoglobin and heme and that the protein may employ both heme-scavenging and one-electron reduction of radicals to achieve this.

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