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      Identification of an immune-regulated phagosomal Rab cascade in macrophages

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          ABSTRACT

          Interferon-γ (IFN-γ) has been shown to regulate phagosome trafficking and function in macrophages, but the molecular mechanisms involved are poorly understood. Here, we identify Rab20 as part of the machinery by which IFN-γ controls phagosome maturation. We found that IFN-γ stimulates the association of Rab20 with early phagosomes in macrophages. By using imaging of single phagosomes in live cells, we found that Rab20 induces an early delay in phagosome maturation and extends the time for which Rab5a and phosphatidylinositol 3-phosphate (PI3P) remain associated with phagosomes. Moreover, Rab20 depletion in macrophages abrogates the delay in phagosome maturation induced by IFN-γ. Finally, we demonstrate that Rab20 interacts with the Rab5a guanine nucleotide exchange factor Rabex-5 (also known as RABGEF1) and that Rab20 knockdown impairs the IFN-γ-dependent recruitment of Rabex-5 and Rab5a into phagosomes. Taken together, here, we uncover Rab20 as a key player in the Rab cascade by which IFN-γ induces a delay in phagosome maturation in macrophages.

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          Most cited references37

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          Rab GTPase regulation of membrane identity.

          S Pfeffer (2013)
          A fundamental question in cell biology is how cells determine membrane compartment identity and the directionality with which cargoes pass through the secretory and endocytic pathways. The discovery of so-called 'Rab cascades' provides a satisfying molecular mechanism that helps to resolve this paradox. One Rab GTPase has the ability to template the localization of the subsequent acting Rab GTPase along a given transport pathway. Thus, in addition to determining compartment identity and functionality, Rab GTPases are likely able to order the events of membrane trafficking. This review will highlight recent advances in our understanding of Rabs and Rab cascades. Copyright © 2013 Elsevier Ltd. All rights reserved.
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            Distinct roles of class I and class III phosphatidylinositol 3-kinases in phagosome formation and maturation

            Phagosomes acquire their microbicidal properties by fusion with lysosomes. Products of phosphatidylinositol 3-kinase (PI 3-kinase) are required for phagosome formation, but their role in maturation is unknown. Using chimeric fluorescent proteins encoding tandem FYVE domains, we found that phosphatidylinositol 3-phosphate (PI[3]P) accumulates greatly but transiently on the phagosomal membrane. Unlike the 3′-phosphoinositides generated by class I PI 3-kinases which are evident in the nascent phagosomal cup, PI(3)P is only detectable after the phagosome has sealed. The class III PI 3-kinase VPS34 was found to be responsible for PI(3)P synthesis and essential for phagolysosome formation. In contrast, selective ablation of class I PI 3-kinase revealed that optimal phagocytosis, but not maturation, requires this type of enzyme. These results highlight the differential functional role of the two families of kinases, and raise the possibility that PI(3)P production by VPS34 may be targeted during the maturation arrest induced by some intracellular parasites.
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              T helper 2 cytokines inhibit autophagic control of intracellular Mycobacterium tuberculosis.

              Autophagy is a recently recognized immune effector mechanism against intracellular pathogens. The role of autophagy in innate immunity has been well established, but the extent of its regulation by the adaptive immune response is less well understood. The T helper 1 (Th1) cell cytokine IFN-gamma induces autophagy in macrophages to eliminate Mycobacterium tuberculosis. Here, we report that Th2 cytokines affect autophagy in macrophages and their ability to control intracellular M. tuberculosis. IL-4 and IL-13 abrogated autophagy and autophagy-mediated killing of intracellular mycobacteria in murine and human macrophages. Inhibition of starvation-induced autophagy by IL-4 and IL-13 was dependent on Akt signaling, whereas the inhibition of IFN-gamma-induced autophagy was Akt independent and signal transducer and activator of transcription 6 (STAT6) dependent. These findings establish a mechanism through which Th1-Th2 polarization differentially affects the immune control of intracellular pathogens.
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                Author and article information

                Journal
                J Cell Sci
                J. Cell. Sci
                joces
                jcs
                Journal of Cell Science
                The Company of Biologists (Bidder Building, 140 Cowley Road, Cambridge, CB4 0DL, UK )
                0021-9533
                1477-9137
                1 May 2014
                1 May 2014
                : 127
                : 9
                : 2071-2082
                Affiliations
                [1 ]Research Group Phagosome Biology, Helmholtz Centre for Infection Research , Inhoffenstrasse 7, 38124 Braunschweig, Germany
                [2 ]Department of Biosciences, University of Oslo , Blindernveien 31, 0371 Oslo, Norway
                [3 ]Division of Mycobacterial Research, Medical Research Council, National Institute for Medical Research , The Ridgeway, London NW7 1AA, UK
                Author notes
                [* ]Author for correspondence ( mgutier@ 123456nimr.mrc.ac.uk )
                Article
                10.1242/jcs.144923
                4004979
                24569883
                0d23c571-98e2-4f05-93b2-8f76ede1a40e
                © 2014. Published by The Company of Biologists Ltd

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 21 October 2013
                : 28 January 2014
                Categories
                Research Article

                Cell biology
                macrophage,rab,phagosome,rabex-5,lysosome
                Cell biology
                macrophage, rab, phagosome, rabex-5, lysosome

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