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顶浆分泌——事实还是假象?

Apocrine secretion--fact or artifact?

作者信息

Aumüller G, Wilhelm B, Seitz J

机构信息

Department of Anatomy and Cell Biology, Philipps-Universität, Marburg, Germany.

出版信息

Ann Anat. 1999 Sep;181(5):437-46. doi: 10.1016/S0940-9602(99)80020-X.

Abstract

In this review, the history of apocrine secretion and the essential categories are briefly mentioned and fused into a more generally applicable terminology. Using the coagulating gland of the male rat as a model, the mechanisms of apocrine secretion, the participation of the cytoskeleton in the formation of the apocrine blebs ("aposomes") and the structure of the secretory proteins, as well as the hormonal regulation of their biosynthesis are described. Apocrine secreted proteins share the following peculiarities: (i) Their biosynthesis and post-translational modification (including an unusual form of glycosylation) take place in the cytoplasm. (ii) Intracellular transport proceeds without participation of the endomembrane system, the Golgi apparatus and secretion granules. (iii) Blood serum derived transsudated albumin entering the secretory cells functions as a carrier of the apocrine-released proteins. Some common molecular features are specific for the apocrine-synthesized proteins studied so far by our group: (a) Their primary sequence is synthesized without a signal peptide. (b) Their N-terminus is blocked by acetylation. (c) The substituting glycanes are neither O- nor N-linked. (d) At least one of the apocrine-synthesized proteins (secretory transglutaminase) contains a glycerol-phosphoinositol (GPI-) anchor. There are a number of still open questions in apocrine secretion, pertaining to (I) the intracellular transport and targeting of the proteins, (II) the coordination of simultaneously occurring apocrine and merocrine secretion in several of the apocrine glands, (III) the biosynthesis of the apical membrane proteins surrounding the aposomes and (IV) the repair mechanisms of the apical cell pole following the release of the aposomes. In conclusion, apocrine release is not an artifact but rather an alternative extrusion mechanism of soluble and membrane-associated proteins, usually linked with sex- or reproductive-related glands, such as the prostate, the mammary glands, apocrine sweat glands or epididymis.

摘要

在本综述中,简要提及了顶浆分泌的历史和基本类别,并将其融合为一个更普遍适用的术语。以雄性大鼠的凝固腺为模型,描述了顶浆分泌的机制、细胞骨架在顶浆小泡(“顶浆体”)形成中的参与以及分泌蛋白的结构,以及它们生物合成的激素调节。顶浆分泌的蛋白质具有以下特点:(i)它们的生物合成和翻译后修饰(包括一种不寻常的糖基化形式)在细胞质中进行。(ii)细胞内运输在没有内膜系统、高尔基体和分泌颗粒参与的情况下进行。(iii)进入分泌细胞的血清衍生漏出白蛋白作为顶浆释放蛋白的载体。我们小组目前研究的顶浆合成蛋白具有一些共同的分子特征:(a)它们的一级序列在没有信号肽的情况下合成。(b)它们的N端被乙酰化阻断。(c)取代聚糖既不是O-连接也不是N-连接。(d)至少一种顶浆合成蛋白(分泌型转谷氨酰胺酶)含有甘油磷酸肌醇(GPI-)锚定。顶浆分泌中仍有许多未解决的问题,涉及(I)蛋白质的细胞内运输和靶向,(II)几种顶浆腺中同时发生的顶浆分泌和局部分泌的协调,(III)围绕顶浆体的顶膜蛋白的生物合成,以及(IV)顶浆体释放后顶细胞极的修复机制。总之,顶浆释放不是一种假象,而是可溶性和膜相关蛋白的一种替代挤出机制,通常与性或生殖相关的腺体有关,如前列腺、乳腺、顶泌汗腺或附睾。

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