Brunauer L S, Moxness M S, Huestis W H
Department of Chemistry, Santa Clara University, California 95053.
Biochemistry. 1994 Apr 19;33(15):4527-32. doi: 10.1021/bi00181a013.
The effects of oxidative damage on membrane phospholipid organization were examined in human erythrocytes. Exposure to H2O2 induced shape changes in these cells; normal discocytes became echinocytic, and stomatocytes generated by foreign phosphatidylserine incorporation reverted to discoid morphology. H2O2 treatment also inhibited phosphatidylserine transport from the outer to inner membrane monolayer, consistent with earlier reports on oxidative sensitivity of the aminophospholipid translocator. The morphological changes are consistent with movement of inner monolayer lipids to the outer monolayer, as might be expected if aminophospholipid sequestration is compromised. However, lipid extraction and prothrombinase activation assays showed no increased exposure of phosphatidylserine on the cell surface. Instead, phosphatidylserine was found associated with the cytosolic fraction of H2O2-treated cells. These observations suggest that oxidative damage alters the lipid organization of erythrocyte membranes, not by randomizing the lipid classes within the bilayer, but by inducing extraction of inner monolayer components into the cytosol.
在人类红细胞中研究了氧化损伤对膜磷脂组织的影响。暴露于过氧化氢会诱导这些细胞发生形态变化;正常的盘状红细胞变成棘状红细胞,而通过掺入外源磷脂酰丝氨酸产生的口形红细胞则恢复为盘状形态。过氧化氢处理还抑制了磷脂酰丝氨酸从外膜单层向内膜单层的转运,这与早期关于氨基磷脂转运体氧化敏感性的报道一致。形态变化与内膜单层脂质向外膜单层的移动一致,如果氨基磷脂隔离受损,可能会出现这种情况。然而,脂质提取和凝血酶原激活试验表明,细胞表面磷脂酰丝氨酸的暴露没有增加。相反,发现磷脂酰丝氨酸与过氧化氢处理细胞的胞质部分相关。这些观察结果表明,氧化损伤改变了红细胞膜的脂质组织,不是通过使双层内的脂质类别随机化,而是通过诱导内膜单层成分进入胞质溶胶。