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1.
PLoS Pathog ; 13(10): e1006700, 2017 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-29084291

RESUMO

Salmonella enterica serovar typhimurium extensively remodels the host late endocytic compartments to establish its vacuolar niche within the host cells conducive for its replication, also known as the Salmonella-containing vacuole (SCV). By maintaining a prolonged interaction with late endosomes and lysosomes of the host cells in the form of interconnected network of tubules (Salmonella-induced filaments or SIFs), Salmonella gains access to both membrane and fluid-phase cargo from these compartments. This is essential for maintaining SCV membrane integrity and for bacterial intravacuolar nutrition. Here, we have identified the multisubunit lysosomal tethering factor-HOPS (HOmotypic fusion and Protein Sorting) complex as a crucial host factor facilitating delivery of late endosomal and lysosomal content to SCVs, providing membrane for SIF formation, and nutrients for intravacuolar bacterial replication. Accordingly, depletion of HOPS subunits significantly reduced the bacterial load in non-phagocytic and phagocytic cells as well as in a mouse model of Salmonella infection. We found that Salmonella effector SifA in complex with its binding partner; SKIP, interacts with HOPS subunit Vps39 and mediates recruitment of this tethering factor to SCV compartments. The lysosomal small GTPase Arl8b that binds to, and promotes membrane localization of Vps41 (and other HOPS subunits) was also required for HOPS recruitment to SCVs and SIFs. Our findings suggest that Salmonella recruits the host late endosomal and lysosomal membrane fusion machinery to its vacuolar niche for access to host membrane and nutrients, ensuring its intracellular survival and replication.


Assuntos
Endossomos/metabolismo , Lisossomos/metabolismo , Complexos Multiproteicos/metabolismo , Infecções por Salmonella/metabolismo , Salmonella typhimurium/metabolismo , Animais , Proteínas de Bactérias/metabolismo , Endossomos/microbiologia , Glicoproteínas/metabolismo , Células HEK293 , Células HeLa , Humanos , Membranas Intracelulares/metabolismo , Lisossomos/microbiologia , Fusão de Membrana , Camundongos , Células RAW 264.7
2.
J Cell Biol ; 216(4): 1051-1070, 2017 04 03.
Artigo em Inglês | MEDLINE | ID: mdl-28325809

RESUMO

Endocytic, autophagic, and phagocytic vesicles move on microtubule tracks to fuse with lysosomes. Small GTPases, such as Rab7 and Arl8b, recruit their downstream effectors to mediate this transport and fusion. However, the potential cross talk between these two GTPases is unclear. Here, we show that the Rab7 effector PLEKHM1 simultaneously binds Rab7 and Arl8b, bringing about clustering and fusion of late endosomes and lysosomes. We show that the N-terminal RUN domain of PLEKHM1 is necessary and sufficient for interaction with Arl8b and its subsequent localization to lysosomes. Notably, we also demonstrate that Arl8b mediates recruitment of HOPS complex to PLEKHM1-positive vesicle contact sites. Consequently, Arl8b binding to PLEKHM1 is required for its function in delivery and, therefore, degradation of endocytic and autophagic cargo in lysosomes. Finally, we also show that PLEKHM1 competes with SKIP for Arl8b binding, which dictates lysosome positioning. These findings suggest that Arl8b, along with its effectors, orchestrates lysosomal transport and fusion.


Assuntos
Fatores de Ribosilação do ADP/metabolismo , Proteínas Adaptadoras de Transdução de Sinal/metabolismo , Lisossomos/metabolismo , Lisossomos/fisiologia , Glicoproteínas de Membrana/metabolismo , Proteínas rab de Ligação ao GTP/metabolismo , Animais , Autofagia/fisiologia , Transporte Biológico/fisiologia , Linhagem Celular , Linhagem Celular Tumoral , Endossomos/metabolismo , Endossomos/fisiologia , Células HEK293 , Células HeLa , Humanos , Microtúbulos/metabolismo , Ligação Proteica/fisiologia , proteínas de unión al GTP Rab7
3.
Database (Oxford) ; 2014: bau011, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24578356

RESUMO

A large repertoire of gene-centric data has been generated in the field of zebrafish biology. Although the bulk of these data are available in the public domain, most of them are not readily accessible or available in nonstandard formats. One major challenge is to unify and integrate these widely scattered data sources. We tested the hypothesis that active community participation could be a viable option to address this challenge. We present here our approach to create standards for assimilation and sharing of information and a system of open standards for database intercommunication. We have attempted to address this challenge by creating a community-centric solution for zebrafish gene annotation. The Zebrafish GenomeWiki is a 'wiki'-based resource, which aims to provide an altruistic shared environment for collective annotation of the zebrafish genes. The Zebrafish GenomeWiki has features that enable users to comment, annotate, edit and rate this gene-centric information. The credits for contributions can be tracked through a transparent microattribution system. In contrast to other wikis, the Zebrafish GenomeWiki is a 'structured wiki' or rather a 'semantic wiki'. The Zebrafish GenomeWiki implements a semantically linked data structure, which in the future would be amenable to semantic search. Database URL: http://genome.igib.res.in/twiki.


Assuntos
Crowdsourcing/métodos , Genoma/genética , Internet , Anotação de Sequência Molecular/métodos , Peixe-Zebra/genética , Animais , Bases de Dados Genéticas
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