果蝇幼虫唾液腺细胞中独立于发育程序的分泌颗粒降解。

IF 3.6 3区 生物学 Q3 CELL BIOLOGY Traffic Pub Date : 2022-12-01 DOI:10.1111/tra.12871
Tamás Csizmadia, Anna Dósa, Erika Farkas, Belián Valentin Csikos, Eszter Adél Kriska, Gábor Juhász, Péter Lőw
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引用次数: 1

摘要

构成分泌和调节分泌都需要能够储存和释放分泌货物的细胞器。在发育过程中,果蝇幼虫的唾液腺最初产生大量含胶的未成熟小分泌颗粒,这些颗粒相互融合,达到正常的3-3.5 μm大小。在分泌爆发后,废弃的胶粒通过一种被称为吞噬的过程直接与晚期内体或溶酶体融合,导致分泌货物的快速降解和再循环。然而,在这些细胞中阻碍内核体到tgn的逆行运输会导致异常小的胶粒,这些胶粒不能相互融合。在这里,我们发现SNARE基因Syntaxin 16 (Syx16)和Synaptobrevin (Syb),小GTPase Rab6和GARP系扎复合物成员Vps53和Scattered (Vps54)的功能缺失都参与逆行运输,通过独立于发育程序的噬噬导致未成熟胶粒的强烈早期降解。此外,这些基因的沉默也会引起幼虫发育过程中的分泌失败和噬噬加速。我们的研究结果更好地理解了分泌、分泌颗粒成熟和降解之间的关系,并为进一步研究其他后生动物的这些联系铺平了道路。
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Developmental program-independent secretory granule degradation in larval salivary gland cells of Drosophila.

Both constitutive and regulated secretion require cell organelles that are able to store and release the secretory cargo. During development, the larval salivary gland of Drosophila initially produces high amount of glue-containing small immature secretory granules, which then fuse with each other and reach their normal 3-3.5 μm in size. Following the burst of secretion, obsolete glue granules directly fuse with late endosomes or lysosomes by a process called crinophagy, which leads to fast degradation and recycling of the secretory cargo. However, hindering of endosome-to-TGN retrograde transport in these cells causes abnormally small glue granules which are not able to fuse with each other. Here, we show that loss of function of the SNARE genes Syntaxin 16 (Syx16) and Synaptobrevin (Syb), the small GTPase Rab6 and the GARP tethering complex members Vps53 and Scattered (Vps54) all involved in retrograde transport cause intense early degradation of immature glue granules via crinophagy independently of the developmental program. Moreover, silencing of these genes also provokes secretory failure and accelerated crinophagy during larval development. Our results provide a better understanding of the relations among secretion, secretory granule maturation and degradation and paves the way for further investigation of these connections in other metazoans.

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来源期刊
Traffic
Traffic 生物-细胞生物学
CiteScore
8.10
自引率
2.20%
发文量
50
审稿时长
2 months
期刊介绍: Traffic encourages and facilitates the publication of papers in any field relating to intracellular transport in health and disease. Traffic papers span disciplines such as developmental biology, neuroscience, innate and adaptive immunity, epithelial cell biology, intracellular pathogens and host-pathogen interactions, among others using any eukaryotic model system. Areas of particular interest include protein, nucleic acid and lipid traffic, molecular motors, intracellular pathogens, intracellular proteolysis, nuclear import and export, cytokinesis and the cell cycle, the interface between signaling and trafficking or localization, protein translocation, the cell biology of adaptive an innate immunity, organelle biogenesis, metabolism, cell polarity and organization, and organelle movement. All aspects of the structural, molecular biology, biochemistry, genetics, morphology, intracellular signaling and relationship to hereditary or infectious diseases will be covered. Manuscripts must provide a clear conceptual or mechanistic advance. The editors will reject papers that require major changes, including addition of significant experimental data or other significant revision. Traffic will consider manuscripts of any length, but encourages authors to limit their papers to 16 typeset pages or less.
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