人红细胞的膜筏。

Q3 Biochemistry, Genetics and Molecular Biology Molecular Membrane Biology Pub Date : 2014-03-01 Epub Date: 2014-04-10 DOI:10.3109/09687688.2014.896485
Annarita Ciana, Cesare Achilli, Giampaolo Minetti
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引用次数: 26

摘要

在质膜膜筏的研究中,很少考虑到用于细胞膜研究的细胞类型——哺乳动物无核红细胞。然而,抗洗涤剂膜(DRM)实际上首先是在人类红细胞中被描述的,作为一种抵抗非离子洗涤剂Triton X-100增溶的部分。这些drm是高密度的不溶性实体,很容易通过离心成粒,这与现在公认的脂质筏状膜组分的概念相反,它们是漂浮在蔗糖梯度的低密度区域的物质。本文从历史的角度回顾了关于人红细胞中膜筏/DRMs的现有文献,描述了为上述差异提供解决方案的实验,并提出了膜筏领域的可能研究途径,从研究最多的活细胞膜模型,红细胞,也可以与其他细胞类型相关。
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Membrane rafts of the human red blood cell.

The cell type of election for the study of cell membranes, the mammalian non-nucleated erythrocyte, has been scarcely considered in the research of membrane rafts of the plasma membrane. However, detergent-resistant-membranes (DRM) were actually first described in human erythrocytes, as a fraction resisting solubilization by the nonionic detergent Triton X-100. These DRMs were insoluble entities of high density, easily pelleted by centrifugation, as opposed to the now accepted concept of lipid raft-like membrane fractions as material floating in low-density regions of sucrose gradients. The present article reviews the available literature on membrane rafts/DRMs in human erythrocytes from an historical point of view, describing the experiments that provided the solution to the above described discrepancy and suggesting possible avenue of research in the field of membrane rafts that, moving from the most studied model of living cell membrane, the erythrocyte's, could be relevant also for other cell types.

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来源期刊
Molecular Membrane Biology
Molecular Membrane Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Cessation. Molecular Membrane Biology provides a forum for high quality research that serves to advance knowledge in molecular aspects of biological membrane structure and function. The journal welcomes submissions of original research papers and reviews in the following areas: • Membrane receptors and signalling • Membrane transporters, pores and channels • Synthesis and structure of membrane proteins • Membrane translocation and targeting • Lipid organisation and asymmetry • Model membranes • Membrane trafficking • Cytoskeletal and extracellular membrane interactions • Cell adhesion and intercellular interactions • Molecular dynamics and molecular modelling of membranes. • Antimicrobial peptides.
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