Truong H T, Ferrell J E, Huestis W H
Blood. 1986 Jan;67(1):214-21.
Metabolic crenation of red cells is reversible; on addition of nutrients, echinocytes recover the normal discoid shape. When the shape recovery takes place in the presence of reducing agents such as dithiothreitol (DTT), morphological change continues until the cells are stomatocytic. The degree of stomatocytosis varies, depending on the cell morphology when the nutrients and reducing agent are added. DTT has minimal effect on the shape of normal discocytes, but in its presence, mildly echinocytic cells become slightly cupped and advanced-stage echinocytes become severely stomatocytic. DTT must be present continuously for development and retention of stomatocytosis; echinocytes preincubated with or metabolically depleted in DTT do not become stomatocytic when supplemented in the absence of DTT, and DTT-induced stomatocytes revert to discocytes when the reducing agent is removed. DTT has no effect on adenosine triphosphate synthesis or equilibrium cell glutathione levels, and the induced stomatocytosis is not inhibited by excluding oxygen from cells during depletion. Spectrin phosphorylation and phosphate turnover are not affected by DTT. The echinocyte-to-discocyte transformation coincides with phosphorylation of membrane inner monolayer lipids (diacylglycerol to phosphatidic acid and phosphatidylinositol to phosphatidylinositol-4,5-bisphosphate). Overphosphorylation of these phospholipids is not responsible for the exaggerated shape recovery seen with reducing agents; phosphorylation of inner monolayer lipids proceeds identically in the presence and absence of DTT.
红细胞的代谢性皱缩是可逆的;添加营养物质后,棘红细胞可恢复正常的盘状形态。当在二硫苏糖醇(DTT)等还原剂存在的情况下发生形态恢复时,形态变化会持续进行,直到细胞变成口形细胞。口形细胞增多的程度各不相同,这取决于添加营养物质和还原剂时的细胞形态。DTT对正常盘状细胞的形态影响极小,但在其存在的情况下,轻度棘红细胞会变得稍有凹陷,而晚期棘红细胞会变成严重的口形细胞。DTT必须持续存在才能使口形细胞增多得以发展和维持;预先用DTT孵育或代谢耗尽DTT的棘红细胞,在没有DTT补充的情况下不会变成口形细胞,而当去除还原剂时,DTT诱导的口形细胞会恢复为盘状细胞。DTT对三磷酸腺苷合成或细胞内谷胱甘肽平衡水平没有影响,并且在耗尽过程中通过排除细胞内的氧气并不能抑制诱导的口形细胞增多。血影蛋白磷酸化和磷酸周转不受DTT影响。棘红细胞向盘状细胞的转变与膜内单分子层脂质的磷酸化(二酰基甘油转变为磷脂酸,磷脂酰肌醇转变为磷脂酰肌醇 - 4,5 - 二磷酸)同时发生。这些磷脂的过度磷酸化并不是还原剂导致的过度形态恢复的原因;在有和没有DTT的情况下,内单分子层脂质的磷酸化过程是相同的。