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遗传性球形红细胞增多症、遗传性椭圆形红细胞增多症和热异形红细胞症中红细胞膜骨架超微结构的改变。

Alteration of the erythrocyte membrane skeletal ultrastructure in hereditary spherocytosis, hereditary elliptocytosis, and pyropoikilocytosis.

作者信息

Liu S C, Derick L H, Agre P, Palek J

机构信息

Department of Biomedical Research, St Elizabeth's Hospital, Boston, MA 02135.

出版信息

Blood. 1990 Jul 1;76(1):198-205.

PMID:2364170
Abstract

The membrane skeleton of normal erythrocytes is largely organized into a hexagonal lattice of junctional complexes (JC) crosslinked by spectrin tetramers, and occasional double tetramers and hexamers. To explore possible skeletal alterations in hereditary spherocytosis (HS), elliptocytosis (HE), and pyropoikilocytosis (HPP), we have studied the ultrastructure of the spread membrane skeletons from a subpopulation of HS patients with a partial spectrin deficiency ranging from 43% to 86% of normal levels, and in patients with HPP who, in addition to a mild spectrin deficiency, also carried a mutant spectrin that was dysfunctional, thus reducing the ability of spectrin dimers to assemble into tetramers. Membrane skeletons derived from Triton-treated erythrocyte ghosts were examined by negative staining electron microscopy. HS membrane skeletons contained structural elements, consisting of JC and spectrin filaments similar to the normal skeleton. However, less spectrin filaments interconnected the JC, and the decrease of spectrin filaments attached to JC appeared to correlate with the severity of spectrin deficiency. Only in severe HS associated with severe spectrin deficiency was the loss of spectrin sufficient enough to disrupt the overall skeletal architecture. In contrast, membrane skeletons prepared from red blood cells (RBCs) of subjects with HPP were strikingly different from HS RBCs with a comparable degree of spectrin deficiency. Although HPP RBCs were only mildly deficient in spectrin, their skeletal lattice was grossly disrupted, in contrast to only mild ultrastructural abnormalities of HS membrane skeletons with a nearly identical degree of spectrin deficiency. Skeletons from patients with common mild HE or asymptomatic carriers, carrying the mutant spectrin but having normal spectrin content, exhibited a moderate disruption of the skeletal lattice. We propose that the above differences in skeletal ultrastructure may underlie differences in the biomechanical properties and morphology of HS, HE, and HPP RBCs.

摘要

正常红细胞的膜骨架主要组织成由血影蛋白四聚体交联的连接复合物(JC)的六边形晶格,偶尔还有双四聚体和六聚体。为了探究遗传性球形红细胞增多症(HS)、椭圆形红细胞增多症(HE)和热异形红细胞增多症(HPP)中可能存在的骨架改变,我们研究了来自部分血影蛋白缺乏程度在正常水平的43%至86%之间的HS患者亚群以及HPP患者(除了轻度血影蛋白缺乏外,还携带功能失调的突变血影蛋白,从而降低了血影蛋白二聚体组装成四聚体的能力)的铺展膜骨架的超微结构。通过负染色电子显微镜检查经Triton处理的红细胞血影得到的膜骨架。HS膜骨架包含与正常骨架相似的由JC和血影蛋白丝组成的结构元件。然而,连接JC的血影蛋白丝较少,且附着于JC的血影蛋白丝的减少似乎与血影蛋白缺乏的严重程度相关。只有在与严重血影蛋白缺乏相关的严重HS中,血影蛋白的缺失才足以破坏整体骨架结构。相比之下,从HPP受试者的红细胞(RBC)制备的膜骨架与具有相当程度血影蛋白缺乏的HS RBC有显著不同。尽管HPP RBC仅轻度缺乏血影蛋白,但其骨架晶格严重破坏,而具有几乎相同程度血影蛋白缺乏的HS膜骨架仅表现出轻度超微结构异常。患有常见轻度HE或无症状携带者的患者,其携带突变血影蛋白但血影蛋白含量正常,其骨架晶格表现出中度破坏。我们认为,上述骨架超微结构的差异可能是HS、HE和HPP RBC生物力学特性和形态差异的基础。

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