| Literature DB >> 15485662 |
Yulia Y Tyurina1, Vladimir A Tyurin, Qing Zhao, Mirjana Djukic, Peter J Quinn, Bruce R Pitt, Valerian E Kagan.
Abstract
Selective oxidation of phosphatidylserine (PS) during apoptosis precedes its externalization in plasma membrane and is essential for the engulfment of apoptotic cells. To experimentally test whether PS oxidation stimulates its externalization via its effects on aminophospholipid translocase (APT) or by enhanced PS scrambling, action of oxidized PS (PSox) was studied using leukemia HL-60 cells and lymphoma Raji cells. Both PS and PSox were equally well recognized by APT. PSox did not inhibit APT. Rate of transmembrane PS diffusion was fourfold higher in cells with integrated PSox than with PS. Thus, PSox acts as a "non-enzymatic scramblase" likely contributing to PS externalization.Entities:
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Year: 2004 PMID： 15485662 DOI： 10.1016/j.bbrc.2004.09.102
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN： 0006-291X Impact factor: 3.575