Biogenesis and Function of Multivesicular Bodies

THE UBIQUITIN SYSTEM

Hershko, A., & Ciechanover, A. (1998) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.67.1.425 · Cited by 8,840

Global analysis of protein localization in budding yeast

Huh, W.-K., Falvo, J. V., Gerke, L. C., Carroll, A. S., Howson, R. W., Weissman, J. S., & O'Shea, E. K. (2003) · Nature · doi:10.1038/nature02026 · Cited by 4,248 · cited 1×

Fate of the transferrin receptor during maturation of sheep reticulocytes in vitro: Selective externalization of the receptor

Pan, B., & Johnstone, R. M. (1983) · Cell · doi:10.1016/0092-8674(83)90040-5 · Cited by 2,042

Proteomic Analysis of Dendritic Cell-Derived Exosomes: A Secreted Subcellular Compartment Distinct from Apoptotic Vesicles

Théry, C., Boussac, M., Véron, P., Ricciardi‐Castagnoli, P., Raposo, G., Garin, J., & Amigorena, S. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.12.7309 · Cited by 1,564

Activated Platelets Release Two Types of Membrane Vesicles: Microvesicles by Surface Shedding and Exosomes Derived From Exocytosis of Multivesicular Bodies and -Granules

Heijnen, H. F. G., Schiel, A. E., Fijnheer, R., Geuze, H. J., & Sixma, J. J. (1999) · Blood · doi:10.1182/blood.v94.11.3791 · Cited by 1,488

Ubiquitin-Dependent Sorting into the Multivesicular Body Pathway Requires the Function of a Conserved Endosomal Protein Sorting Complex, ESCRT-I

Katzmann, D. J., Babst, M., & Emr, S. D. (2001) · Cell · doi:10.1016/s0092-8674(01)00434-2 · Cited by 1,473

Selective Enrichment of Tetraspan Proteins on the Internal Vesicles of Multivesicular Endosomes and on Exosomes Secreted by Human B-lymphocytes

Escola, J.-M., Kleijmeer, M. J., Stoorvogel, W., Griffith, J. M., Yoshie, O., & Geuze, H. J. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.32.20121 · Cited by 1,228

Receptor downregulation and multivesicular-body sorting

Katzmann, D. J., Odorizzi, G., & Emr, S. D. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm973 · Cited by 1,201

Regulation of Membrane Protein Transport by Ubiquitin and Ubiquitin-Binding Proteins

Hicke, L., & Dunn, R. (2003) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.19.110701.154617 · Cited by 1,131

Localization of phosphatidylinositol 3-phosphate in yeast and mammalian cells

Gillooly, D. J., Morrow, I. C., Lindsay, M., Gould, R., Bryant, N. J., Gaullier, J., Parton, R. G., & Stenmark, H. (2000) · The EMBO Journal · doi:10.1093/emboj/19.17.4577 · Cited by 1,031

Extracellular Vesicles: Recent Developments in Technology and Perspectives for Cancer Liquid Biopsy

Nazarenko, I. A. (2019) · Recent results in cancer research/Recent Results in Cancer Research · doi:10.1007/978-3-030-26439-0_17 · Cited by 39

Oxidative damage of lysosomes in regulated cell death systems: Pathophysiology and pharmacologic interventions

Nagakannan, P., Tabeshmehr, P., & Eftekharpour, E. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.04.001 · Cited by 41

Ubiquitination Regulates the Morphogenesis and Function of Sperm Organelles

Nakamura, N. (2013) · Cells · doi:10.3390/cells2040732 · Cited by 42

Involvement of Vps33a in the Fusion of Uroplakin‐Degrading Multivesicular Bodies with Lysosomes

Guo, X., Tu, L., Gumper, I., Plesken, H., Novak, E. K., Chintala, S., Swank, R. T., Pastores, G. M., Torres, P., Izumi, T., et al. (2009) · Traffic · doi:10.1111/j.1600-0854.2009.00950.x · Cited by 39

Virus Entry by Endocytosis

Nicola, A. V., Aguilar, H. C., Mercer, J., Ryckman, B. J., & Wiethoff, C. M. (2013) · Advances in Virology · doi:10.1155/2013/469538 · Cited by 41

The late endocytic Rab39a GTPase regulates multivesicular bodies-chlamydial inclusion interaction and bacterial growth

Tudela, J. G., Capmany, A., Romao, M., Quintero, C. A., Miserey‐Lenkei, S., Raposo, G., Goud, B., & Damiani, M. (2015) · Journal of Cell Science · doi:10.1242/jcs.170092 · Cited by 38

The Myxovirus‐Resistance Protein, MX 1, is a Component of Exosomes Secreted by Uterine Epithelial Cells

Racicot, K. E., Schmitt, A. P., & OTT, T. L. (2012) · American Journal of Reproductive Immunology · doi:10.1111/j.1600-0897.2012.01109.x · Cited by 41

Mechanisms of Action of EGFR Tyrosine Kinase Receptor Incorporated in Extracellular Vesicles

Zanetti-Domingues, L. C., Bonner, S. E., Martin-Fernandez, M. L., & Huber, V. (2020) · Cells · doi:10.3390/cells9112505 · Cited by 41

Circulating RNA biomarkers in diffuse large B-cell lymphoma: a systematic review

Decruyenaere, P., Offner, F. C., & Vandesompele, J. (2021) · Experimental Hematology and Oncology · doi:10.1186/s40164-021-00208-3 · Cited by 42

Large organellar changes occur during mild heat shock in yeast

Keuenhof, K., Berglund, L. L., Hill, S. M., Schneider, K. L., Widlund, P. O., Nyström, T., & Höög, J. L. (2021) · Journal of Cell Science · doi:10.1242/jcs.258325 · Cited by 36

Membrane-Elasticity Model of Coatless Vesicle Budding Induced by ESCRT Complexes

Różycki, B., Bouřa, E., Hurley, J. H., & Hummer, G. (2012) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002736 · Cited by 38

'A life or death decision' for pollen tubes in S-RNase-based self-incompatibility

Chen, G., Zhang, B., Zhao, Z., Sui, Z., Zhang, H., & Xue, Y. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp381 · Cited by 37

Exosome-Derived LncRNAs in Lung Cancer

Fan, T. T., Sun, N., & He, J. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.01728 · Cited by 37

Ancient Evolutionary Origin and Properties of Universally Produced Natural Exosomes Contribute to Their Therapeutic Superiority Compared to Artificial Nanoparticles

Askenase, P. W. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22031429 · Cited by 41

Gold nanoparticles (AuNPs) impair LPS-driven immune responses by promoting a tolerogenic-like dendritic cell phenotype with altered endosomal structures

Michelini, S., Barbero, F., Prinelli, A., Steiner, P., Weiss, R., Verwanger, T., Andosch, A., Lütz‐Meindl, U., Puntes, V., Drobne, D., et al. (2021) · Nanoscale · doi:10.1039/d0nr09153g · Cited by 38

Wnt Signaling Translocates Lys48-Linked Polyubiquitinated Proteins to the Lysosomal Pathway

Kim, H., Vick, P., Hedtke, J. P., Ploper, D., & Robertis, E. M. D. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.04.048 · Cited by 37

Genomic analysis of severe hypersensitivity to hygromycin B reveals linkage to vacuolar defects and new vacuolar gene functions in Saccharomyces cerevisiae

Bañuelos, M. G., Moreno, D., Olson, D. K., Nguyen, Q., Ricarte, F. R., Aguilera-Sandoval, C. R., & Gharakhanian, E. (2009) · Current Genetics · doi:10.1007/s00294-009-0285-3 · Cited by 37

Intracytoplasmic Trapping of Influenza Virus by a Lipophilic Derivative of Aglycoristocetin

Vanderlinden, E., Vanstreels, E., Boons, E., ter Veer, W., Huckriede, A. L. W., Daelemans, D., Lommel, A. V., Rőth, E., Sztaricskai, F., Herczegh, P., et al. (2012) · Journal of Virology · doi:10.1128/jvi.07032-11 · Cited by 37

Exosome-Based Macromolecular neurotherapeutic drug delivery approaches in overcoming the Blood-Brain barrier for treating brain disorders

Yadav, D. K., Vijayalakshmi, R., Sahu, K. K., Sure, P., Chahal, K., Yadav, R. K., Sucheta, Dubey, A., Jha, M., & Pradhan, M. (2024) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2024.114298 · Cited by 38

ESCRT-dependent targeting of plasma membrane localized KCa3.1 to the lysosomes

Balut, C., Gao, Y., Murray, S., Thibodeau, P. H., & Devor, D. C. (2010) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00120.2010 · Cited by 36

Cell Proliferation and Epidermal Growth Factor Signaling in Non-small Cell Lung Adenocarcinoma Cell Lines Are Dependent on Rin1

Tomshine, J. C., Severson, S. R., Wigle, D. A., Sun, Z., Beleford, D. T., Shridhar, V., & Horazdovsky, B. F. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.033514 · Cited by 36

Release of HIV-1 sequestered in the vesicles of oral and genital mucosal epithelial cells by epithelial-lymphocyte interaction

Yasen, A., Herrera, R., Rosbe, K. W., Lien, K., & Tugizov, S. M. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006247 · Cited by 36

The human lung mucosa drives differential Mycobacterium tuberculosis infection outcome in the alveolar epithelium

Scordo, J. M., Olmo-Fontánez, A. M., Kelley, H. V., Sidiki, S., Arcos, J., Akhter, A., Wewers, M. D., & Torrelles, J. B. (2019) · Mucosal Immunology · doi:10.1038/s41385-019-0156-2 · Cited by 36

Focus on exosomes: novel pathogenic components of leukemia.

Yang, C., Yang, H., Liu, J., Zhu, L., Shicang, Y., Zhang, X., & Gao, L. (2019) · PubMed Central · Cited by 36

Proteome of ubiquitin/MVB pathway: possible involvement of iron-induced ubiquitylation of transferrin receptor in lysosomal degradation

Tachiyama, R., Ishikawa, D., Matsumoto, M., Nakayama, K. I., Yoshimori, T., Yokota, S., Himeno, M., Tanaka, Y., & Fujita, H. (2011) · Genes to Cells · doi:10.1111/j.1365-2443.2011.01499.x · Cited by 36

Acetylcholine α7 nicotinic and dopamine D2 receptors are targeted to many of the same postsynaptic dendrites and astrocytes in the rodent prefrontal cortex

Duffy, Á., Fitzgerald, M. L., Chan, J., Robinson, D. C., Milner, T. A., Mackie, K., & Pickel, V. M. (2011) · Synapse · doi:10.1002/syn.20977 · Cited by 35

Identification of an AAA ATPase VPS4B-Dependent Pathway That Modulates Epidermal Growth Factor Receptor Abundance and Signaling during Hypoxia

Lin, H., Li, X., Chen, J.-L., Sun, X., Cooper, F. N., Chen, Y.-R., Zhang, W., Chung, Y., Li, A., Cheng, C.-T., et al. (2012) · Molecular and Cellular Biology · doi:10.1128/mcb.06053-11 · Cited by 39

Reduced endosomal microautophagy activity in aging associates with enhanced exocyst‐mediated protein secretion

Krause, G. J., Diaz, A., Jafari, M., Khawaja, R. R., Agullo‐Pascual, E., Santiago‐Fernández, O., Richards, A. L., Chen, K., Dmitriev, P., Sun, Y., et al. (2022) · Aging Cell · doi:10.1111/acel.13713 · Cited by 35

Molecular Pathways Implicated in Radioresistance of Glioblastoma Multiforme: What Is the Role of Extracellular Vesicles?

Burko, P., D’Amico, G., Miltykh, I. S., Scalia, F., de Macario, E. C., Macario, A. J. L., Giglia, G., Cappello, F., & Bavisotto, C. C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054883 · Cited by 37

Exosome-Mediated Antigen Delivery: Unveiling Novel Strategies in Viral Infection Control and Vaccine Design

Safadi, D. E., Krejbich, M., MOKHTARI, A., Lagrave, A., Hirigoyen, U., Lebeau, G., Viranaïcken, W., & Trotot, P. K. (2024) · Vaccines · doi:10.3390/vaccines12030280 · Cited by 41

Mild Fixation and Permeabilization Protocol for Preserving Structures of Endosomes, Focal Adhesions, and Actin Filaments During Immunofluorescence Analysis

Scheffler, J. M., Schiefermeier-Mach, N., & Huber, L. A. (2014) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/b978-0-12-397925-4.00006-7 · Cited by 35

Intersection of the Multivesicular Body Pathway and Lipid Homeostasis in RNA Replication by a Positive-Strand RNA Virus

Wang, X., Diaz, A., Hao, L., Gancarz, B., den Boon, J. A., & Ahlquist, P. (2011) · Journal of Virology · doi:10.1128/jvi.02031-10 · Cited by 35

Exosomes Are Unlikely Involved in Intercellular Nef Transfer

Luo, X., Fan, Y., Park, I.-W., & He, J. J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0124436 · Cited by 35

Rab11 and Lysotracker Markers Reveal Correlation between Endosomal Pathways and Transfection Efficiency of Surface-Functionalized Cationic Liposome–DNA Nanoparticles

Majzoub, R. N., Wonder, E. A., Ewert, K. K., Kotamraju, V. R., Teesalu, T., & Safinya, C. R. (2016) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.6b04441 · Cited by 35

The sphingosine 1-phosphate receptor 2 is shed in exosomes from breast cancer cells and is N-terminally processed to a short constitutively active form that promotes extracellular signal regulated kinase activation and DNA synthesis in fibroblasts

Elburi, A. H. A., Adams, D. R., Smith, D. H., Tate, R. J., Mullin, M., Pyne, S., & Pyne, N. J. (2018) · Oncotarget · doi:10.18632/oncotarget.25658 · Cited by 38

A glucose-starvation response governs endocytic trafficking and eisosomal retention of surface cargoes in budding yeast

Laidlaw, K. M. E., Bisinski, D. D., Shashkova, S., Paine, K. M., Veillon, M. A., Leake, M. C., & MacDonald, C. (2020) · Journal of Cell Science · doi:10.1242/jcs.257733 · Cited by 34

The Immunomodulation Potential of Exosomes in Tumor Microenvironment

Wang, M., & Zhang, B. (2021) · Journal of Immunology Research · doi:10.1155/2021/3710372 · Cited by 35

Label-free, ultrahigh-speed, 3D observation of bidirectional and correlated intracellular cargo transport by coherent brightfield microscopy

Huang, Y., Zhuo, G., Chou, C.-Y., Lin, C.-H., & Hsieh, C. (2017) · Nanoscale · doi:10.1039/c7nr00604g · Cited by 35

Circulating Exosome Cargoes Contain Functionally Diverse Cancer Biomarkers: From Biogenesis and Function to Purification and Potential Translational Utility

Mitchell, M. I., Ma, J., Carter, C. L., & Loudig, O. D. (2022) · Cancers · doi:10.3390/cancers14143350 · Cited by 34

The Role of Exosome-Derived microRNA on Lung Cancer Metastasis Progression

Martínez-Espinosa, I., Serrato, J. A., & Ortíz-Quintero, B. (2023) · Biomolecules · doi:10.3390/biom13111574 · Cited by 34

Roles of Cdc48 in Regulated Protein Degradation in Yeast

Buchberger, A. (2013) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-94-007-5940-4_8 · Cited by 33

Endosomes and Autophagy: Regulators of Pulmonary Endothelial Cell Homeostasis in Health and Disease

Chichger, H., Rounds, S., & Harrington, E. O. (2019) · Antioxidants and Redox Signaling · doi:10.1089/ars.2019.7817 · Cited by 33

Interrelation between extracellular vesicles miRNAs with chronic lung diseases

Dhar, R., Mukherjee, S., Mukerjee, N., Mukherjee, D., Devi, A., Ashraf, G. M., Alserihi, R. F., Tayeb, H. H., Hashem, A. M., Alexiou, A. T., et al. (2022) · Journal of Cellular Physiology · doi:10.1002/jcp.30867 · Cited by 34

Release of damaged mitochondrial DNA: A novel factor in stimulating inflammatory response

Li, W., Li, Y., Zhao, J., Liao, J., Wen, W., Chen, Y., & Cui, H. (2024) · Pathology - Research and Practice · doi:10.1016/j.prp.2024.155330 · Cited by 34

Role of SMURF1 ubiquitin ligase in BMP receptor trafficking and signaling

Murakami, K., & Etlinger, J. D. (2018) · Cellular Signalling · doi:10.1016/j.cellsig.2018.10.015 · Cited by 33

Role of the Feline Immunodeficiency Virus L-domain in the presence or absence of Gag processing: involvement of ubiquitin and Nedd4-2s ligase in viral egress

Calistri, A., Vecchio, C. D., Salata, C., Celestino, M., Celegato, M., Göttlinger, H., Palù, G., & Parolin, C. (2009) · Journal of Cellular Physiology · doi:10.1002/jcp.21587 · Cited by 34

Vaccinia Virus E2L Null Mutants Exhibit a Major Reduction in Extracellular Virion Formation and Virus Spread

Domi, A., Weisberg, A. S., & Moss, B. (2008) · Journal of Virology · doi:10.1128/jvi.00037-08 · Cited by 33

Extracellular vesicles in hematological malignancies

Litwińska, Z., Łuczkowska, K., & Machaliński, B. (2018) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.1080/10428194.2018.1459606 · Cited by 35

New insights into the morphology of Trypanosoma cruzi reservosome

Sant’Anna, C., Pereira, M. G., Lemgruber, L., de Souza, W., & Cunha‐e‐Silva, N. L. (2008) · Microscopy Research and Technique · doi:10.1002/jemt.20592 · Cited by 33

The role of exosomes and MYC in therapy resistance of acute myeloid leukemia: Challenges and opportunities

Mudgapalli, N., Nallasamy, P., Chava, H., Chava, S. P., Pathania, A. S., Gunda, V., Gorantla, S., Pandey, M. K., Gupta, S. C., & Challagundla, K. B. (2019) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2019.10.001 · Cited by 31

Therapeutic Effects of Hypoxic and Pro-Inflammatory Priming of Mesenchymal Stem Cell-Derived Extracellular Vesicles in Inflammatory Arthritis

Kay, A. G., Treadwell, K., Roach, P., Morgan, R., Lodge, R. W., Hyland, M., Piccinini, A. M., Forsyth, N. R., & Kehoe, O. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms23010126 · Cited by 32

Secretory Granule Membrane Protein Recycles through Multivesicular Bodies

Bäck, N., Rajagopal, C., Mains, R. E., & Eipper, B. A. (2010) · Traffic · doi:10.1111/j.1600-0854.2010.01066.x · Cited by 32

Fluorescent, phosphorescent, magnetic resonance contrast and radioactive tracer labelling of extracellular vesicles

Wardhani, K. A., Levina, A., Grau, G. E., & Lay, P. A. (2024) · Chemical Society Reviews · doi:10.1039/d2cs00238h · Cited by 34

The Rubicon–WIPI axis regulates exosome biogenesis during ageing

Yanagawa, K., Kuma, A., Hamasaki, M., Kita, S., Yamamuro, T., Nishino, K., Nakamura, S., Omori, H., Kaminishi, T., Oikawa, S., et al. (2024) · Nature Cell Biology · doi:10.1038/s41556-024-01481-0 · Cited by 34

Chapter 1 Macromolecular Trafficking and Immune Evasion in African Trypanosomes

Field, M. C., Lumb, J. H., Adung’a, V. O., Jones, N. G., & Engstler, M. (2009) · International review of cytology · doi:10.1016/s1937-6448(09)78001-3 · Cited by 32

The integral function of the endocytic recycling compartment is regulated by RFFL-mediated ubiquitylation of Rab11 effectors

Sakai, R., Fukuda, R., Unida, S., Aki, M., Ono, Y., Endo, A., Kusumi, S., Koga, D., Fukushima, T., Komada, M., et al. (2019) · Journal of Cell Science · doi:10.1242/jcs.228007 · Cited by 30

Repurposing Cationic Amphiphilic Drugs and Derivatives to Engage Lysosomal Cell Death in Cancer Treatment

Hu, M., & Carraway, K. L. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.605361 · Cited by 33

The Role of Exosomes in Lysosomal Storage Disorders

Gleason, A. M., Woo, E. G., McKinney, C. E., & Sidransky, E. (2021) · Biomolecules · doi:10.3390/biom11040576 · Cited by 31

Unravelling Secretion in Cryptococcus neoformans: More than One Way to Skin a Cat

Rodrigues, M. L., & Djordjevic, J. T. (2011) · Mycopathologia · doi:10.1007/s11046-011-9468-9 · Cited by 31

Retrograde trafficking and quality control of yeast synaptobrevin, Snc1, are conferred by its transmembrane domain

Ma, M., & Burd, C. G. (2019) · Molecular Biology of the Cell · doi:10.1091/mbc.e19-02-0117 · Cited by 30

Aphidius ervi Teratocytes Release Enolase and Fatty Acid Binding Protein Through Exosomal Vesicles

Salvia, R., Grimaldi, A., Girardello, R., Scieuzo, C., Scala, A., Bufo, S. A., Vogel, H., & Falabella, P. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00715 · Cited by 30

Role of extracellular vesicles in osteosarcoma

Yang, Q., Liu, J., Wu, B., Wang, X., Jiang, Y., & Zhu, D. (2022) · International Journal of Medical Sciences · doi:10.7150/ijms.74137 · Cited by 31

Out of the ESCPE room: Emerging roles of endosomal SNX‐BARs in receptor transport and host–pathogen interaction

Simonetti, B., Daly, J. L., & Cullen, P. J. (2023) · Traffic · doi:10.1111/tra.12885 · Cited by 39

Interactome of the Plant-specific ESCRT-III Component AtVPS2.2 in Arabidopsis thaliana

Ibl, V., Csaszar, E., Schlager, N., Neubert, S., Spitzer, C., & Hauser, M. (2011) · Journal of Proteome Research · doi:10.1021/pr200845n · Cited by 32

Cellular evidence for nano-scale exosome secretion and interactions with spermatozoa in the epididymis of the Chinese soft-shelled turtle,Pelodiscus sinensis

Chen, H., Yang, P., Chu, X., Huang, Y., Liu, T., Zhang, Q., Li, Q., Hu, L., Waqas, Y., Ahmed, N., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.8092 · Cited by 30

Transglutaminase type 2 in the regulation of proteostasis

D’Eletto, M., Rossin, F., Fedorova, O., Farrace, M. G., & Piacentini, M. (2018) · Biological Chemistry · doi:10.1515/hsz-2018-0217 · Cited by 32

“Liquid Biopsy” of White Matter Hyperintensity in Functionally Normal Elders

Elahi, F. M., Casaletto, K. B., Altendahl, M., Staffaroni, A. M., Fletcher, E. M., Filshtein, T. J., Glymour, M. M., Miller, B. L., Hinman, J. D., DeCarli, C. S., et al. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00343 · Cited by 28

The Conserved YAGL Motif in Human Metapneumovirus Is Required for Higher-Order Cellular Assemblies of the Matrix Protein and for Virion Production

Sabo, Y., Ehrlich, M., & Bacharach, E. (2011) · Journal of Virology · doi:10.1128/jvi.02694-10 · Cited by 30

The Obligate Intracellular Bacterial Pathogen Anaplasma phagocytophilum Exploits Host Cell Multivesicular Body Biogenesis for Proliferation and Dissemination

Read, C. B., Lind, M. C. H., Chiarelli, T. J., Izac, J. R., Adcox, H. E., Marconi, R. T., & Carlyon, J. A. (2022) · mBio · doi:10.1128/mbio.02961-22 · Cited by 29

High‐Resolution Fractionation of Signaling Endosomes Containing Different Receptors

McCaffrey, G., Welker, J. E., Scott, J., van der Salm, L., & Grimes, M. L. (2009) · Traffic · doi:10.1111/j.1600-0854.2009.00909.x · Cited by 29

Trafficking of a multifunctional protein by endosomal microautophagy: linking two independent unconventional secretory pathways

Chauhan, A. S., Kumar, M., Chaudhary, S., Dhiman, A., Patidar, A., Jakhar, P., Jaswal, P., Sharma, K., Sheokand, N., Malhotra, H., et al. (2019) · The FASEB Journal · doi:10.1096/fj.201802102r · Cited by 29

Proteomics reveals time-dependent protein corona changes in the intracellular pathway

Marques, R. D. C., Hüppe, N., Speth, K. R., Oberländer, J., Lieberwirth, I., Landfester, K., & Mailänder, V. (2023) · Acta Biomaterialia · doi:10.1016/j.actbio.2023.10.010 · Cited by 28

Intramembrane proteolysis within lysosomes

Schröder, B., & Säftig, P. (2016) · Ageing Research Reviews · doi:10.1016/j.arr.2016.04.012 · Cited by 28

Generation of the heterogeneity of extracellular vesicles by membrane organization and sorting machineries

Harada, Y., Suzuki, T., Fukushige, T., Kizuka, Y., Yagi, H., Yamamoto, M., Kondo, K., Inoue, H., Kato, K., Taniguchi, N., et al. (2019) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2019.01.015 · Cited by 28

Lysosomes in T Cell Immunity and Aging

Jin, J., Zhang, H., Weyand, C. M., & Goronzy, J. J. (2021) · Frontiers in Aging · doi:10.3389/fragi.2021.809539 · Cited by 30

The Yeast vps Class E Mutants: The Beginning of the Molecular Genetic Analysis of Multivesicular Body Biogenesis

Coonrod, E. M., & Stevens, T. H. (2010) · Molecular Biology of the Cell · doi:10.1091/mbc.e09-07-0603 · Cited by 31

SNX31: A Novel Sorting Nexin Associated with the Uroplakin-Degrading Multivesicular Bodies in Terminally Differentiated Urothelial Cells

Vieira, N., Deng, F., Liang, F., Liao, Y., Chang, J. S., Zhou, G., Zheng, W., Simon, J.-P., Ding, M., Wu, X., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0099644 · Cited by 30

A Genome-Wide Immunodetection Screen in S. cerevisiae Uncovers Novel Genes Involved in Lysosomal Vacuole Function and Morphology

Ricarte, F. R., Menjivar, R. E., Chhun, S., Soreta, T., Oliveira, L., Hsueh, T., Serranilla, M., & Gharakhanian, E. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023696 · Cited by 27

Clinical Applications of Liquid Biopsy in Colorectal Cancer Screening: Current Challenges and Future Perspectives

Galoș, D., Gorzo, A., Bălăcescu, O., & Sur, D. G. (2022) · Cells · doi:10.3390/cells11213493 · Cited by 28

Rab39a and Rab39b Display Different Intracellular Distribution and Function in Sphingolipids and Phospholipids Transport

Tudela, J. G., BUONFIGLI, J., Lujan, A. L., Bivou, M. A., Cebrián, I., Capmany, A., & Damiani, M. T. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20071688 · Cited by 28

Cooperation and Interplay between EGFR Signalling and Extracellular Vesicle Biogenesis in Cancer

Zanetti-Domingues, L. C., Bonner, S. E., Iyer, R. S., Martin-Fernandez, M. L., & Huber, V. (2020) · Cells · doi:10.3390/cells9122639 · Cited by 29

Dynamic membranes: the multiple roles of P4 and P5 ATPases

López‐Marqués, R. L., Davis, J. A., Harper, J. F., & Palmgren, M. B. (2020) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiaa065 · Cited by 27

An Updated View of the Importance of Vesicular Trafficking and Transport and Their Role in Immune-Mediated Diseases: Potential Therapeutic Interventions

Ortega, M. A., Fraile‐Μartinez, O., Montero, C. G., Álvarez-Mon, M. Á., Gomez-Lahoz, A. M., Albillos, A., Lahera, G., Quintero, J., Monserrat, J., Guijarro, L. G., et al. (2022) · Membranes · doi:10.3390/membranes12060552 · Cited by 31

Brucella Egresses from Host Cells Exploiting Multivesicular Bodies

Spera, J. M., Guaimas, F. F., Czibener, C., & Ugalde, J. E. (2023) · mBio · doi:10.1128/mbio.03338-22 · Cited by 27

Ultrastructure of dorsal root ganglia

Haberberger, R. V., Kuramatilake, J., Barry, C., & Matusica, D. (2023) · Cell and Tissue Research · doi:10.1007/s00441-023-03770-w · Cited by 27

Differences between migrasome, a ‘new organelle’, and exosome

Xu, X., Wu, T., Lin, R., Zhu, S., Ji, J., Jin, D., Huang, M., Zheng, W., Ni, W., Jiang, F., et al. (2023) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.17942 · Cited by 27

Septin6 and Septin7 GTP Binding Proteins Regulate AP-3- and ESCRT-Dependent Multivesicular Body Biogenesis

Traikov, S., Stange, C., Wassmer, T., Paul‐Gilloteaux, P., Salamero, J., Raposo, G., & Hoflack, B. (2014) · PLoS ONE · doi:10.1371/journal.pone.0109372 · Cited by 29

Terminating protein ubiquitination

Stringer, D. K., & Piper, R. C. (2011) · Cell Cycle · doi:10.4161/cc.10.18.17191 · Cited by 27

Distinct features of multivesicular body‐lysosome fusion revealed by a new cell‐free content‐mixing assay

Karim, M. A., Samyn, D. R., Mattie, S., & Brett, C. L. (2017) · Traffic · doi:10.1111/tra.12543 · Cited by 27

Proteome from patients with metabolic syndrome is regulated by quantity and quality of dietary lipids

Rangel-Zúñiga, O. A., Camargo, A., Marı́n, C., Peña‐Orihuela, P. J., Pérez‐Martínez, P., Delgado‐Lista, J., González-Guardia, L., Yubero‐Serrano, E. M., Tinahones, F. J., Malagón, M. M., et al. (2015) · BMC Genomics · doi:10.1186/s12864-015-1725-8 · Cited by 28

Autophagy differentially regulates TNF receptor Fn14 by distinct mammalian Atg8 proteins

Winer, H. Y., Fraiberg, M., Abada, A., Dadosh, T., Tamim-Yecheskel, B.-C., & Elazar, Z. (2018) · Nature Communications · doi:10.1038/s41467-018-06275-1 · Cited by 25

Autophagy and Exosomes: Cross-Regulated Pathways Playing Major Roles in Hepatic Stellate Cells Activation and Liver Fibrosis

Mastoridou, E. M., GOUSSIA, A. C., Glantzounis, G. K., Kanavaros, P., & Charchanti, A. V. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2021.801340 · Cited by 27

Role of exosomes and its emerging therapeutic applications in the pathophysiology of non-infectious diseases

Shivji, G. G., Dhar, R., & Devi, A. (2022) · Biomarkers · doi:10.1080/1354750x.2022.2067233 · Cited by 26

Chloroplasts Protein Quality Control and Turnover: A Multitude of Mechanisms

Fu, Y., Li, X., Fan, B., Zhu, C., & Chen, Z. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23147760 · Cited by 26

Protein-protein-interaction Network Organization of the Hypusine Modification System

Sievert, H., Venz, S., Barradas, O. P., Dhople, V. M., Schaletzky, M., Nagel, C., Braig, M., Preukschas, M., Pällmann, N., Bokemeyer, C., et al. (2012) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m112.019059 · Cited by 25

A small molecule compound IMB-LA inhibits HIV-1 infection by preventing viral Vpu from antagonizing the host restriction factor BST-2

Mi, Z., Ding, J., Zhang, Q., Zhao, J., Ma, L., Yu, H., Liu, Z., Shan, G., Li, X., Zhou, J., et al. (2015) · Scientific Reports · doi:10.1038/srep18499 · Cited by 26

Exosomes as a therapeutic tool to promote neurorestoration and cognitive function in neurological conditions: Achieve two ends with a single effort

Fallahi, S., Zangbar, H. S., Farajdokht, F., Rahbarghazi‬, R., Mohaddes, G., & Ghiasi, R. (2024) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14752 · Cited by 27

Extracellular vesicles in β cell biology: Role of lipids in vesicle biogenesis, cargo, and intercellular signaling

Aguirre, R. S., Kulkarni, A., Becker, M. W., Lei, X., Sarkar, S., Ramanadham, S., Phelps, E. A., Nakayasu, E. S., Sims, E. K., & Mirmira, R. G. (2022) · Molecular Metabolism · doi:10.1016/j.molmet.2022.101545 · Cited by 25

Cycling of Dense Core Vesicles Involved in Somatic Exocytosis of Serotonin by Leech Neurons

Trueta, C., Kuffler, D. P., & De‐Miguel, F. F. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00175 · Cited by 25

Mechanistic understanding and significance of small peptides interaction with MHC class II molecules for therapeutic applications

Afridi, S., Hoessli, D. C., & Hameed, M. W. (2016) · Immunological Reviews · doi:10.1111/imr.12435 · Cited by 25

Ubiquitin-Mediated Vacuolar Sorting and Degradation

Klionsky, D. J. (2003) · CRC Press eBooks · doi:10.1201/9781498713276-20

Multivesicular Bodies and Multivesicular Endosomes: The "Ins and Outs" of Endosomal Traffic

Stahl, P. D., & Barbieri, M. A. (2002) · Science Signaling · doi:10.1126/scisignal.1412002pe32 · Cited by 12

Biogenesis of Multivesicular Body and Protein Sorting: No One of ESCRT,Vps4 and Ubiquitination Can Be Missed

Heng, X., 张春霞, 冯凡, 袁弋, Yang, Z. H. O. U., Liu, X., Zhu, K., 姚勤, & 陈克平 (2013) · PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS

Multivesicular Body (MSB)

(2008) · Springer eBooks · doi:10.1007/978-1-4020-6754-9_10962

Multivesicular bodies: co-ordinated progression to maturity

Woodman, P. G., & Futter, C. E. (2008) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2008.04.001 · Cited by 214