4.5 Article

The late endosomal adaptor p14 is a macrophage host-defense factor against Salmonella infection

期刊

JOURNAL OF CELL SCIENCE
卷 125, 期 11, 页码 2698-2708

出版社

COMPANY OF BIOLOGISTS LTD
DOI: 10.1242/jcs.100073

关键词

LAMTOR2; Macrophage; MAPK; Phagosome; Salmonella

资金

  1. Austrian Research Funds 'Cell Proliferation and Cell Death in Tumors' [SFB021, FWF-P19664, P19486-B12]

向作者/读者索取更多资源

The outcome of an infection depends on the balance between host resistance and bacterial virulence. Here, we show that the late endosomal adaptor p14 (also known as LAMTOR2) is one of the components for cellular host defense against the intracellular pathogen Salmonella enterica serovar Typhimurium. During Salmonella infection, the complex of p14 and MP1 is required for the accurately timed transport of Salmonella through the endolysosomal system. Loss of p14 opens a time window that allows Salmonella to populate a replication niche, in which early and late antimicrobial effector systems, comprising NADPH phagocytic oxidase and inducible nitric oxide synthase, respectively, are inappropriately activated. Thus, p14 supports the accurate transport of Salmonella through the endolysosomal system, thereby limiting bacterial replication in both, professional phagocytes and in non-phagocytic cells in vitro, and helps mice to successfully battle Salmonella infection in vivo.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Developmental Biology

Papillae revisited and the nature of the adhesive secreting collocytes

Fan Zeng, Julia Wunderer, Willi Salvenmoser, Michael W. Hess, Peter Ladurner, Ute Rothbaecher

DEVELOPMENTAL BIOLOGY (2019)

Article Multidisciplinary Sciences

A mechanism for temporary bioadhesion

Julia Wunderer, Birgit Lengerer, Robert Pjeta, Philip Bertemes, Leopold Kremser, Herbert Lindner, Thomas Ederth, Michael W. Hess, David Stock, Willi Salvenmoser, Peter Ladurner

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2019)

Article Neurosciences

Subcellular Localization of Sprouty2 in Human Glioma Cells

Barbara Hausott, Jong-Whi Park, Taras Valovka, Martin Offterdinger, Michael W. Hess, Stephan Geley, Lars Klimaschewski

FRONTIERS IN MOLECULAR NEUROSCIENCE (2019)

Article Cardiac & Cardiovascular Systems

miR-19a-3p containing exosomes improve function of ischaemic myocardium upon shock wave therapy

Can Gollmann-Tepekoeylue, Leo Poelzl, Michael Graber, Jakob Hirsch, Felix Naegele, Daniela Lobenwein, Michael W. Hess, Michael J. Blumer, Elke Kirchmair, Johannes Zipperle, Carina Hromada, Severin Muehleder, Hubert Hackl, Martin Hermann, Hemse Al Khamisi, Martin Foerster, Michael Lichtenauer, Rainer Mittermayr, Patrick Paulus, Helga Fritsch, Nikolaos Bonaros, Rudolf Kirchmair, Joost P. G. Sluijter, Sean Davidson, Michael Grimm, Johannes Holfeld

CARDIOVASCULAR RESEARCH (2020)

Article Biochemistry & Molecular Biology

LAMTOR/Ragulator regulates lipid metabolism in macrophages and foam cell differentiation

Giorgia Lamberti, Cedric H. De Smet, Mihaela Angelova, Leopold Kremser, Nicole Taub, Caroline Herrmann, Michael W. Hess, Johannes Rainer, Ivan Tancevski, Ruerdiger Schweigreiter, Reinhard Kofler, Thomas Schmiedinger, Ilja Vietor, Zlatko Trajanoski, Christer S. Ejsing, Herbert H. Lindner, Lukas A. Huber, Taras Stasyk

FEBS LETTERS (2020)

Article Biology

Temporary adhesion of the proseriate flatworm Minona ileanae

Robert Pjeta, Julia Wunderer, Philip Bertemes, Teresa Hofer, Willi Salvenmoser, Birgit Lengerer, Stefan Coassin, Gertraud Erhart, Christian Beisel, Daniel Sobral, Leopold Kremser, Herbert Lindner, Marco Curini-Galletti, Claus-Peter Stelzer, Michael W. Hess, Peter Ladurner

PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES (2019)

Review Cell Biology

Lysosomal size matters

Mariana E. G. de Araujo, Gudrun Liebscher, Michael W. Hess, Lukas A. Huber

TRAFFIC (2020)

Article Medicine, General & Internal

Advanced Microscopy for Liver and Gut Ultrastructural Pathology in Patients with MVID and PFIC Caused by MYO5B Mutations

Michael W. Hess, Iris M. Krainer, Przemyslaw A. Filipek, Barbara Witting, Karin Gutleben, Ilja Vietor, Heinz Zoller, Denise Aldrian, Ekkehard Sturm, James R. Goldenring, Andreas R. Janecke, Thomas Mueller, Lukas A. Huber, Georg F. Vogel

Summary: The study thoroughly characterized the ultrastructural and immuno-cytochemical phenotype of hepatocytes and duodenal enterocytes from a unique case of an adult MYO5B-PFIC patient. Advanced methods were used in combination with standard procedures to reveal various abnormalities related to this rare disease.

JOURNAL OF CLINICAL MEDICINE (2021)

Article Immunology

P80 Natural Essence Exerts Efficient Anti-HIV-1- as Well as Adjuvant Effects in DCs

Viktoria Zaderer, Wilfried Posch, Ronald Gstir, Przemyslaw A. Filipek, Guenther K. Bonn, Pornanong Aramwit, Lukas A. Huber, Doris Wilflingseder

Summary: The natural essence P80 has been shown to affect the function of DCs, with high concentrations leading to increased cell death and moderate concentrations showing effective antiviral effects. P80 natural essence significantly enhances DC maturation and co-stimulatory capacity through p38 MAPK phosphorylation, providing a defense against HIV-1 virus.

VACCINES (2021)

Article Cell Biology

The SZT2 Interactome Unravels New Functions of the KICSTOR Complex

Cecilia Cattelani, Dominik Lesiak, Gudrun Liebscher, Isabel I. Singer, Taras Stasyk, Moritz H. Wallnoefer, Alexander M. Heberle, Corrado Corti, Michael W. Hess, Kristian Pfaller, Marcel Kwiatkowski, Peter P. Pramstaller, Andrew A. Hicks, Kathrin Thedieck, Thomas Muller, Lukas A. Huber, Mariana Eca Guimaraes de Araujo

Summary: The study reveals the role of SZT2 in the amino acid-sensing branch of mTORC1, with mutations in this gene causing severe neurodevelopmental and epileptic encephalopathy. Further analysis indicates enhanced mTORC1 signaling activation and higher levels of autophagic components in SZT2 ablated cells.
Article Multidisciplinary Sciences

Structure of the lysosomal mTORC1-TFEB-Rag-Ragulator megacomplex

Zhicheng Cui, Gennaro Napolitano, Mariana E. G. de Araujo, Alessandra Esposito, Jlenia Monfregola, Lukas A. A. Huber, Andrea Ballabio, James H. H. Hurley

Summary: The transcription factor TFEB is phosphorylated by mTORC1, which is unique in its mechanism and dependent on the activation of FLCN6,7. The cryogenic-electron microscopy analysis reveals that two Rag-Ragulator complexes present each TFEB molecule to mTOR active site. The non-canonical Rag dimer binds the first helix of TFEB with a RagC(GDP)-dependent aspartate clamp and plays a crucial role in TFEB phosphorylation.

NATURE (2023)

Article Biology

A CRISPR screen in intestinal epithelial cells identifies novel factors for polarity and apical transport

Katharina M. C. Klee, Michael W. Hess, Michael Lohmueller, Sebastian Herzog, Kristian Pfaller, Thomas Mueller, Georg F. Vogel, Lukas A. Huber, Michel Bagnat

Summary: In this study, we conducted a genome-wide CRISPR/Cas9 screen combined with FACS to identify novel regulators of epithelial polarization and protein secretion in human polarized epithelial cells. Through high-resolution microscopy, we confirmed the role of TM9SF4, anoctamin 8, and ARHGAP33 in epithelial polarization and apical cargo secretion. This study provides a powerful tool for studying these processes and offers a dataset for the investigation of novel congenital diseases associated with epithelial polarization and polarized transport.
Article Genetics & Heredity

SLC5A1 Variants in Turkish Patients with Congenital Glucose-Galactose Malabsorption

Ferda O. Hosnut, Andreas R. Janecke, Gulseren Sahin, Georg F. Vogel, Naz G. Lafci, Paul Bichler, Thomas Mueller, Lukas A. Huber, Taras Valovka, Aysel U. Aksu

Summary: Congenital glucose-galactose malabsorption is a rare autosomal recessive disorder caused by mutations in SLC5A1 gene. Our study reports clinical and molecular data from 11 affected individuals in four unrelated Turkish families. Two novel SLC5A1 missense variants, p.Gly43Arg and p.Ala92Val, were identified in two families and linked to the disease. Our findings expand the mutational spectrum of this rare disorder.
暂无数据