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蛋白质激素在分泌颗粒中的储存:浓缩和分选机制。

Protein hormone storage in secretory granules: mechanisms for concentration and sorting.

作者信息

Dannies P S

机构信息

Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

出版信息

Endocr Rev. 1999 Feb;20(1):3-21. doi: 10.1210/edrv.20.1.0354.

Abstract

Recent findings in cell biology have demonstrated there are several kinds of active sorting from the trans-Golgi network in all cells. The presence of several sorting pathways, using more than one sorting signal, in neuroendocrine cells means that mutations that direct a hormone to a constitutive pathway instead of a regulated one may not simply be interpreted as a signal for sorting to a regulated pathway. The use of three-dimensional electron microscopy of lactotrophs and the possibility that the trans-Golgi network is consumed during sorting has suggested a major role for hormone aggregation, not only as a sorting mechanism, but also as a mechanism for granule formation, in that other transport vesicles may bud from the trans-Golgi network, leaving the aggregated protein as the dense core granule. If aggregation plays such a role, it is unclear how it works in cases where the prohormone must be processed one or more times; does a porous aggregate or colloid form? Obtaining information about the kinds of aggregates that occur in cells is difficult, because at this time there is not a definitive way of knowing whether an aggregate that occurs in solution also occurs in cells. Although secretory granule proteins tend to aggregate relatively easily in solution, the separate treatment of different secretory granule proteins in the same cell make it unlikely that aggregation is a purely passive process, but suggests that the process of aggregation of each hormone is actively controlled in cells. Even if the ability to aggregate accounts for most of the sorting of cargo-secretory granule proteins into granules, other sorting must still occur to get correct membrane proteins necessary for transport and exocytosis into secretory granule membranes. Possible recognition sites for these secretory granule membrane proteins include the cargo itself in an aggregated form, membrane lipids in some unrecognized way, or the proteins and factors that specifically control aggregation of the cargo.

摘要

细胞生物学领域的最新研究发现,所有细胞的反式高尔基体网络中都存在几种活跃的分选过程。神经内分泌细胞中存在多种分选途径,且使用不止一种分选信号,这意味着那些将激素导向组成型途径而非调节型途径的突变,可能不能简单地被解释为分选至调节型途径的信号。对催乳细胞进行三维电子显微镜观察,以及反式高尔基体网络在分选过程中可能被消耗的情况,表明激素聚集不仅作为一种分选机制,而且作为颗粒形成的一种机制发挥着重要作用,因为其他运输小泡可能从反式高尔基体网络出芽,留下聚集的蛋白质作为致密核心颗粒。如果聚集起到这样的作用,那么在激素原必须经过一次或多次加工的情况下,它是如何发挥作用的尚不清楚;会形成多孔聚集体还是胶体呢?获取细胞中发生的聚集体种类的信息很困难,因为目前还没有确定的方法来知晓溶液中出现的聚集体在细胞中是否也会出现。尽管分泌颗粒蛋白在溶液中相对容易聚集,但同一细胞中不同分泌颗粒蛋白的单独处理表明,聚集不太可能是一个纯粹的被动过程,而是暗示细胞中每种激素的聚集过程是受到积极控制的。即使聚集能力解释了大多数货物分泌颗粒蛋白分选进入颗粒的过程,仍必须进行其他分选,以将运输和胞吐所需的正确膜蛋白纳入分泌颗粒膜中。这些分泌颗粒膜蛋白可能的识别位点包括聚集形式的货物本身、某种未被识别方式的膜脂,或特异性控制货物聚集的蛋白质和因子。

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