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囊泡在人嗜碱性粒细胞分泌中的作用。

A role for vesicles in human basophil secretion.

作者信息

Dvorak A M

机构信息

Department of Pathology, East Campus, Beth Israel Deaconess Medical Center and Harvard Medical School, 330 Brookline Avenue, Boston, MA 02215, USA.

出版信息

Cell Tissue Res. 1998 Jul;293(1):1-22. doi: 10.1007/s004410051093.

Abstract

The evidence for vesicular transport as a mechanism for secretion by human basophils is reviewed. Initially, direct electron-microscopic inspection of experimentally produced and sequentially biopsied contact allergy skin lesions revealed a unique form of secretion termed piecemeal degranulation, characterized by the slow emptying of secretory granule contents (with retention of empty containers) in the absence of extrusion of entire granules. Budding of small vesicles to/from secretory granules was observed, and cytoplasmic vesicles were abundant. A generalized degranulation model was proposed to unify classical regulated secretion and this new form of secretion. Investigation of the mechanism(s) of secretion from human basophils required the development of numerous tools and resources. Chief among these were: (a) isolation and purification of circulating basophils; (b) identification of specific growth factors to increase the supply of this rare granulocyte; (c) understanding of secretogogue mechanisms and reliable analyses of secreted basophil products; and (d) development of ultrastructural preparations allowing imaging of small vesicles and quantifiable small electron-dense tags for granule materials in small vesicles. Applications of these tools to well-defined models of basophil secretion have established a role for vesicles as a mechanism for effecting secretion of histamine and the Charcot-Leyden crystal protein from activated human basophils.

摘要

本文综述了囊泡运输作为人类嗜碱性粒细胞分泌机制的证据。最初,通过对实验诱导并经连续活检的接触性过敏皮肤损伤进行直接电子显微镜检查,发现了一种独特的分泌形式,称为逐片脱颗粒,其特征是在没有整个颗粒挤出的情况下,分泌颗粒内容物缓慢排空(空容器保留)。观察到分泌颗粒与小囊泡之间的出芽现象,并且细胞质囊泡丰富。提出了一个通用的脱颗粒模型,以统一经典的调节性分泌和这种新的分泌形式。对人类嗜碱性粒细胞分泌机制的研究需要开发大量工具和资源。其中主要包括:(a)循环嗜碱性粒细胞的分离和纯化;(b)鉴定特定生长因子以增加这种稀有粒细胞的供应;(c)了解促分泌机制并对分泌的嗜碱性粒细胞产物进行可靠分析;(d)开发超微结构制剂,以便对小囊泡进行成像,并对小囊泡中的颗粒物质进行可量化的小电子致密标记。将这些工具应用于明确的嗜碱性粒细胞分泌模型,已确定囊泡作为从活化的人类嗜碱性粒细胞中分泌组胺和嗜酸性粒细胞趋化因子的一种机制所起的作用。

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