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聚(乙二醇)-胆固醇诱导棘红细胞的超微结构研究

Ultrastructural study of echinocytes induced by poly (ethylene glycol)-cholesterol.

作者信息

Baba Takeshi, Terada Nobuo, Fujii Yasuhisa, Ohno Nobuhiko, Ohno Shinichi, Sato Satoshi B

机构信息

Department of Anatomy, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, 1110 Shimokato, Tamaho, 409-3898 Yamanashi, Japan.

出版信息

Histochem Cell Biol. 2004 Dec;122(6):587-92. doi: 10.1007/s00418-004-0723-8. Epub 2004 Nov 18.

Abstract

Poly (ethylene glycol)-cholesterol (PEG-Chol) consists of a hydrophilic PEG and hydrophobic cholesterol moiety. When PEG-Chol was applied to erythrocytes, the reagent quantitatively induced protrusions by exclusively distributing in the outer monolayer of the membrane. This kind of response has been regarded as a general response that reduces the stress of expansion of the outer monolayer. However, the relationship between the membrane architecture and the distribution of such molecules is unknown. In this study, we examined the distribution of tagged PEG-Chol along the shape change pathway. The echinocytic shape was initiated by the initial formation of bumps on the rim of the discoid, which subsequently elongated as protrusions. These protrusions contained aggregates of granular structures, which appeared to accommodate the increase in the outer monolayer area. At higher concentrations, PEG-Chol further induced sphero-echinocytosis that resulted in numerous branched protrusion processes. We found that PEG-Chol was exclusively distributed in these protrusions and, in particular, accumulated at the tips. These results suggested that externally intercalated PEG-Chol was sequestrated from erythrocytes as membrane protrusions through an as-yet-unknown mechanism.

摘要

聚(乙二醇)-胆固醇(PEG-Chol)由亲水性的聚乙二醇和疏水性的胆固醇部分组成。当PEG-Chol应用于红细胞时,该试剂通过仅分布在膜的外单层中定量诱导突起。这种反应被认为是一种普遍反应,可减轻外单层扩张的压力。然而,膜结构与此类分子分布之间的关系尚不清楚。在本研究中,我们沿着形状变化途径研究了标记的PEG-Chol的分布。棘状细胞形态由盘状边缘上最初形成的凸起引发,这些凸起随后作为突起伸长。这些突起包含颗粒状结构的聚集体,似乎适应了外单层面积的增加。在较高浓度下,PEG-Chol进一步诱导球形棘状红细胞增多症,导致许多分支突起过程。我们发现PEG-Chol仅分布在这些突起中,特别是在尖端积累。这些结果表明,外部插入的PEG-Chol通过一种尚不清楚的机制作为膜突起从红细胞中隔离出来。

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