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溶酶体生物发生过程中内体的重塑涉及由rab5调控的“吻-跑”融合事件。

Remodeling of endosomes during lysosome biogenesis involves 'kiss and run' fusion events regulated by rab5.

作者信息

Duclos Sophie, Corsini Rachel, Desjardins Michel

机构信息

Département de pathologie et biologie cellulaire, Université de Montréal, CP 6128, Succ. Centre ville, Montréal, QC, H3C 3J7, Canada.

出版信息

J Cell Sci. 2003 Mar 1;116(Pt 5):907-18. doi: 10.1242/jcs.00259.

Abstract

The small GTPase rab5 has been shown to play key roles in the function of both endocytic and phagocytic organelles. Although these organelles share several additional common features, different processes have been proposed to explain their biogenesis. In the present study, we provide evidence that lysosome biogenesis involves mechanisms similar to those previously described for the formation of phagolysosomes. Transient interactions ('kiss and run') between endocytic organelles are shown to occur during lysosome biogenesis. These interactions are regulated initially by the GTPase activity of rab5, as demonstrated by the loss of size-selective fusion between endosomes in cells expressing a GTPase-deficient mutant of rab5. Endocytic compartments in these cells sequentially display properties of early and late endosomes. However, the formation of lysosomes and the sorting of endocytic solute materials to small electron dense vacuoles are not affected by the rab5 mutation. Together, our results indicate that endosome maturation occurs during the early part of lysosome biogenesis. This process involves transient fusion events regulated, in part, by the small GTPase rab5.

摘要

小GTP酶rab5已被证明在胞吞和吞噬细胞器的功能中发挥关键作用。尽管这些细胞器还有其他几个共同特征,但人们提出了不同的过程来解释它们的生物发生。在本研究中,我们提供证据表明溶酶体生物发生涉及的机制类似于先前描述的吞噬溶酶体形成机制。在溶酶体生物发生过程中,胞吞细胞器之间会发生短暂相互作用(“吻跑”)。如在表达rab5的GTP酶缺陷突变体的细胞中,内体之间大小选择性融合的丧失所证明,这些相互作用最初受rab5的GTP酶活性调节。这些细胞中的胞吞区室依次表现出早期和晚期内体的特性。然而,溶酶体的形成以及胞吞溶质物质向小电子致密液泡的分选不受rab5突变的影响。总之,我们的结果表明内体成熟发生在溶酶体生物发生的早期阶段。这个过程涉及部分由小GTP酶rab5调节的短暂融合事件。

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