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  1. Artikel: Spatial organization of adenylyl cyclase and its impact on dopamine signaling in neurons.

    Ripoll, Léa / von Zastrow, Mark

    bioRxiv : the preprint server for biology

    2023  

    Abstract: The cAMP cascade is widely recognized to transduce its physiological effects locally through spatially limited cAMP gradients. However, little is known about how the adenylyl cyclase enzymes, which initiate cAMP gradients, are localized. Here we answer ... ...

    Abstract The cAMP cascade is widely recognized to transduce its physiological effects locally through spatially limited cAMP gradients. However, little is known about how the adenylyl cyclase enzymes, which initiate cAMP gradients, are localized. Here we answer this question in physiologically relevant striatal neurons and delineate how AC localization impacts downstream signaling functions. We show that the major striatal AC isoforms are differentially sorted between ciliary and extraciliary domains of the plasma membrane, and that AC9 is uniquely targeted to endosomes. We identify key sorting determinants in the N-terminal cytoplasmic domain responsible for isoform-specific localization. We also show that AC9-containing endosomes accumulate activated dopamine receptors and form an elaborately intertwined network with juxtanuclear PKA stores bound to Golgi membranes. Finally, we show that endosomal localization is critical for AC9 to selectively elevate PKA activity in the nucleus relative to the cytoplasm. These results reveal a precise spatial landscape of the cAMP cascade in neurons and a key role of AC localization in directing downstream signal transduction to the nucleus.
    Sprache Englisch
    Erscheinungsdatum 2023-12-06
    Erscheinungsland United States
    Dokumenttyp Preprint
    DOI 10.1101/2023.12.06.570478
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Illuminating the dark side of recycling endosomes.

    Ripoll, Léa / Heiligenstein, Xavier / Raposo, Graça / Delevoye, Cédric

    Cell cycle (Georgetown, Tex.)

    2016  Band 15, Heft 10, Seite(n) 1309–1310

    Mesh-Begriff(e) Animals ; Annexin A2/metabolism ; Carrier Proteins/genetics ; Cell Line, Tumor ; Endosomes/metabolism ; HeLa Cells ; Humans ; Intracellular Signaling Peptides and Proteins ; Kinesin/genetics ; Kinesin/metabolism ; Lectins/genetics ; Melanins/biosynthesis ; Melanocytes/metabolism ; Melanosomes/metabolism ; Mice ; Nerve Tissue Proteins/metabolism
    Chemische Substanzen ANXA2 protein, human ; Annexin A2 ; BLOC1S1 protein, human ; Bloc1s6 protein, mouse ; Carrier Proteins ; Intracellular Signaling Peptides and Proteins ; KIF13A protein, human ; KIF13A protein, mouse ; Lectins ; Melanins ; Nerve Tissue Proteins ; Kinesin (EC 3.6.4.4)
    Sprache Englisch
    Erscheinungsdatum 2016-05-17
    Erscheinungsland United States
    Dokumenttyp Editorial
    ZDB-ID 2146183-1
    ISSN 1551-4005 ; 1538-4101 ; 1554-8627
    ISSN (online) 1551-4005
    ISSN 1538-4101 ; 1554-8627
    DOI 10.1080/15384101.2016.1160682
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: AP-1/KIF13A Blocking Peptides Impair Melanosome Maturation and Melanin Synthesis.

    Campagne, Cécile / Ripoll, Léa / Gilles-Marsens, Floriane / Raposo, Graça / Delevoye, Cédric

    International journal of molecular sciences

    2018  Band 19, Heft 2

    Abstract: Melanocytes are specialized cells that generate unique organelles called melanosomes in which melanin is synthesized and stored. Melanosome biogenesis and melanocyte pigmentation require the transport and delivery of melanin synthesizing enzymes, such as ...

    Abstract Melanocytes are specialized cells that generate unique organelles called melanosomes in which melanin is synthesized and stored. Melanosome biogenesis and melanocyte pigmentation require the transport and delivery of melanin synthesizing enzymes, such as tyrosinase and related proteins (e.g., TYRP1), from endosomes to maturing melanosomes. Among the proteins controlling endosome-melanosome transport, AP-1 together with KIF13A coordinates the endosomal sorting and trafficking of TYRP1 to melanosomes. We identify here β1-adaptin AP-1 subunit-derived peptides of 5 amino acids that block the interaction of KIF13A with AP-1 in cells. Incubating these peptides with human MNT-1 cells or 3D-reconstructed pigmented epidermis decreases pigmentation by impacting the maturation of melanosomes in fully pigmented organelles. This study highlights that peptides targeting the intracellular trafficking of melanocytes are candidate molecules to tune pigmentation in health and disease.
    Mesh-Begriff(e) Adaptor Protein Complex 1/metabolism ; Adaptor Protein Complex beta Subunits/chemistry ; Adaptor Protein Complex beta Subunits/metabolism ; Endosomes/metabolism ; HeLa Cells ; Humans ; Kinesin/metabolism ; Melanins/biosynthesis ; Melanosomes/drug effects ; Melanosomes/metabolism ; Peptides/pharmacology ; Protein Transport
    Chemische Substanzen Adaptor Protein Complex 1 ; Adaptor Protein Complex beta Subunits ; KIF13A protein, human ; Melanins ; Peptides ; Kinesin (EC 3.6.4.4)
    Sprache Englisch
    Erscheinungsdatum 2018-02-14
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms19020568
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Myosin VI and branched actin filaments mediate membrane constriction and fission of melanosomal tubule carriers.

    Ripoll, Léa / Heiligenstein, Xavier / Hurbain, Ilse / Domingues, Lia / Figon, Florent / Petersen, Karl J / Dennis, Megan K / Houdusse, Anne / Marks, Michael S / Raposo, Graça / Delevoye, Cédric

    The Journal of cell biology

    2018  Band 217, Heft 8, Seite(n) 2709–2726

    Abstract: Vesicular and tubular transport intermediates regulate organellar cargo dynamics. Transport carrier release involves local and profound membrane remodeling before fission. Pinching the neck of a budding tubule or vesicle requires mechanical forces, ... ...

    Abstract Vesicular and tubular transport intermediates regulate organellar cargo dynamics. Transport carrier release involves local and profound membrane remodeling before fission. Pinching the neck of a budding tubule or vesicle requires mechanical forces, likely exerted by the action of molecular motors on the cytoskeleton. Here, we show that myosin VI, together with branched actin filaments, constricts the membrane of tubular carriers that are then released from melanosomes, the pigment containing lysosome-related organelles of melanocytes. By combining superresolution fluorescence microscopy, correlative light and electron microscopy, and biochemical analyses, we find that myosin VI motor activity mediates severing by constricting the neck of the tubule at specific melanosomal subdomains. Pinching of the tubules involves the cooperation of the myosin adaptor optineurin and the activity of actin nucleation machineries, including the WASH and Arp2/3 complexes. The fission and release of these tubules allows for the export of components from melanosomes, such as the SNARE VAMP7, and promotes melanosome maturation and transfer to keratinocytes. Our data reveal a new myosin VI- and actin-dependent membrane fission mechanism required for organelle function.
    Mesh-Begriff(e) Actin Cytoskeleton/metabolism ; Actin Cytoskeleton/physiology ; Cell Line ; Humans ; Melanosomes/metabolism ; Melanosomes/ultrastructure ; Microtubules ; Myosin Heavy Chains/genetics ; Myosin Heavy Chains/metabolism ; Myosin Heavy Chains/physiology ; Transcription Factor TFIIIA/metabolism ; Transcription Factor TFIIIA/physiology
    Chemische Substanzen OPTN protein, human ; Transcription Factor TFIIIA ; myosin VI ; Myosin Heavy Chains (EC 3.6.4.1)
    Sprache Englisch
    Erscheinungsdatum 2018-06-06
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 218154-x
    ISSN 1540-8140 ; 0021-9525
    ISSN (online) 1540-8140
    ISSN 0021-9525
    DOI 10.1083/jcb.201709055
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel ; Online: BLOC-1 Brings Together the Actin and Microtubule Cytoskeletons to Generate Recycling Endosomes.

    Delevoye, Cédric / Heiligenstein, Xavier / Ripoll, Léa / Gilles-Marsens, Floriane / Dennis, Megan K / Linares, Ricardo A / Derman, Laura / Gokhale, Avanti / Morel, Etienne / Faundez, Victor / Marks, Michael S / Raposo, Graça

    Current biology : CB

    2016  Band 26, Heft 1, Seite(n) 1–13

    Abstract: Recycling endosomes consist of a tubular network that emerges from vacuolar sorting endosomes and diverts cargoes toward the cell surface, the Golgi, or lysosome-related organelles. How recycling tubules are formed remains unknown. We show that recycling ...

    Abstract Recycling endosomes consist of a tubular network that emerges from vacuolar sorting endosomes and diverts cargoes toward the cell surface, the Golgi, or lysosome-related organelles. How recycling tubules are formed remains unknown. We show that recycling endosome biogenesis requires the protein complex BLOC-1. Mutations in BLOC-1 subunits underlie an inherited disorder characterized by albinism, the Hermansky-Pudlak Syndrome, and are associated with schizophrenia risk. We show here that BLOC-1 coordinates the kinesin KIF13A-dependent pulling of endosomal tubules along microtubules to the Annexin A2/actin-dependent stabilization and detachment of recycling tubules. These components cooperate to extend, stabilize and form tubular endosomal carriers that function in cargo recycling and in the biogenesis of pigment granules in melanocytic cells. By shaping recycling endosomal tubules, our data reveal that dysfunction of the BLOC-1-KIF13A-Annexin A2 molecular network underlies the pathophysiology of neurological and pigmentary disorders.
    Mesh-Begriff(e) Actins/metabolism ; Annexin A2/metabolism ; Cell Membrane/metabolism ; Endosomes/metabolism ; Golgi Apparatus/metabolism ; HeLa Cells ; Humans ; Kinesin/metabolism ; Lysosomes/metabolism ; Melanocytes/metabolism ; Microtubules/metabolism ; Nerve Tissue Proteins/metabolism ; Protein Transport
    Chemische Substanzen ANXA2 protein, human ; Actins ; Annexin A2 ; BLOC1S1 protein, human ; KIF13A protein, human ; Nerve Tissue Proteins ; Kinesin (EC 3.6.4.4)
    Sprache Englisch
    Erscheinungsdatum 2016-01-11
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 1071731-6
    ISSN 1879-0445 ; 0960-9822
    ISSN (online) 1879-0445
    ISSN 0960-9822
    DOI 10.1016/j.cub.2015.11.020
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: Membrane protrusion powers clathrin-independent endocytosis of interleukin-2 receptor.

    Basquin, Cyril / Trichet, Michaël / Vihinen, Helena / Malardé, Valérie / Lagache, Thibault / Ripoll, Léa / Jokitalo, Eija / Olivo-Marin, Jean-Christophe / Gautreau, Alexis / Sauvonnet, Nathalie

    The EMBO journal

    2015  Band 34, Heft 16, Seite(n) 2147–2161

    Abstract: Endocytosis controls many functions including nutrient uptake, cell division, migration and signal transduction. A clathrin- and caveolin-independent endocytosis pathway is used by important physiological cargos, including interleukin-2 receptors (IL-2R). ...

    Abstract Endocytosis controls many functions including nutrient uptake, cell division, migration and signal transduction. A clathrin- and caveolin-independent endocytosis pathway is used by important physiological cargos, including interleukin-2 receptors (IL-2R). However, this process lacks morphological and dynamic data. Our electron microscopy (EM) and tomography studies reveal that IL-2R-pits and vesicles are initiated at the base of protrusions. We identify the WAVE complex as a specific endocytic actor. The WAVE complex interacts with IL-2R, via a WAVE-interacting receptor sequence (WIRS) present in the receptor polypeptide, and allows for receptor clustering close to membrane protrusions. In addition, using total internal reflection fluorescent microscopy (TIRF) and automated analysis we demonstrate that two timely distinct bursts of actin polymerization are required during IL-2R uptake, promoted first by the WAVE complex and then by N-WASP. Finally, our data reveal that dynamin acts as a transition controller for the recruitment of Arp2/3 activators required for IL-2R endocytosis. Altogether, our work identifies the spatio-temporal specific role of factors initiating clathrin-independent endocytosis by a unique mechanism that does not depend on the deformation of a flat membrane, but rather on that of membrane protrusions.
    Mesh-Begriff(e) Actins/metabolism ; Cell Line ; Cell Membrane/chemistry ; Cell Membrane/metabolism ; Cell Membrane/ultrastructure ; Electron Microscope Tomography ; Endocytosis ; Humans ; Microscopy, Electron, Transmission ; Microscopy, Fluorescence ; Protein Interaction Mapping ; Protein Multimerization ; Receptors, Interleukin-2/metabolism ; Wiskott-Aldrich Syndrome Protein Family/metabolism
    Chemische Substanzen Actins ; Receptors, Interleukin-2 ; Wiskott-Aldrich Syndrome Protein Family
    Sprache Englisch
    Erscheinungsdatum 2015-06-29
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 586044-1
    ISSN 1460-2075 ; 0261-4189
    ISSN (online) 1460-2075
    ISSN 0261-4189
    DOI 10.15252/embj.201490788
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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