Recruitment of CD63 to Cryptococcus neoformans phagosomes requires acidification

Mechanisms of phagocytosis in macrophages

Aderem, A., & Underhill, D. M. (1999) · Annual Review of Immunology · doi:10.1146/annurev.immunol.17.1.593 · Cited by 2,854 · see citing works

A monomeric red fluorescent protein

Campbell, R. E., Tour, O., Palmer, A. E., Steinbach, P. A., Baird, G. S., Zacharias, D. A., & Tsien, R. Y. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.082243699 · Cited by 2,346 · see citing works

Bafilomycins: a class of inhibitors of membrane ATPases from microorganisms, animal cells, and plant cells.

Bowman, E. J., Siebers, A., & Altendorf, K. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.21.7972 · Cited by 1,792 · see citing works

The Toll-like receptor 2 is recruited to macrophage phagosomes and discriminates between pathogens

Underhill, D. M., Ozinsky, A., Hajjar, A. M., Stevens, A. M., Wilson, C. B., Bassetti, M., & Aderem, A. A. (1999) · Nature · doi:10.1038/44605 · Cited by 1,369 · see citing works

Tetraspanin functions and associated microdomains

Hemler, M. E. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1736 · Cited by 1,355 · see citing works

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 · see citing works

Bacterial Invasion: The Paradigms of Enteroinvasive Pathogens

Cossart, P., & Sansonetti, P. (2004) · Science · doi:10.1126/science.1090124 · Cited by 1,002 · see citing works

Regulation of Phagosome Maturation by Signals from Toll-Like Receptors

Blander, J. M., & Medzhitov, R. (2004) · Science · doi:10.1126/science.1096158 · Cited by 991 · see citing works

Characterization of the Mycobacterium tuberculosis phagosome and evidence that phagosomal maturation is inhibited.

Clemens, D. L., & Horwitz, M. A. (1995) · The Journal of Experimental Medicine · doi:10.1084/jem.181.1.257 · Cited by 681 · see citing works

Phagosome maturation: aging gracefully

Vieira, O. V., Botelho, R. J., & Grinstein, S. (2002) · Biochemical Journal · doi:10.1042/bj20020691 · Cited by 675 · see citing works

A membrane protein required for dislocation of misfolded proteins from the ER

Lilley, B. N., & Ploegh, H. L. (2004) · Nature · doi:10.1038/nature02592 · Cited by 674 · see citing works

Mechanism of phagolysosome biogenesis block by viable Mycobacterium tuberculosis

Vergne, I., Chua, J., Lee, H.-H., Lucas, M., Belisle, J. T., & Deretic, V. P. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409716102 · Cited by 537 · see citing works

Molecular characterization of the human macrophage mannose receptor: demonstration of multiple carbohydrate recognition-like domains and phagocytosis of yeasts in Cos-1 cells.

Ezekowitz, R. A. B., Sastry, K., Bailly, P., & Warner, A. (1990) · The Journal of Experimental Medicine · doi:10.1084/jem.172.6.1785 · Cited by 501 · see citing works

Transport of Peptide-MHC Class II Complexes in Developing Dendritic Cells

Turley, S. J., Inaba, K., Garrett, W. S., Ebersold, M. W., Unternaehrer, J., Steinman, R. M., & Mellman, I. (2000) · Science · doi:10.1126/science.288.5465.522 · Cited by 477 · see citing works

V-ATPase interacts with ARNO and Arf6 in early endosomes and regulates the protein degradative pathway

Hurtado‐Lorenzo, A., Skinner, M. A., Annan, J. E., Futai, M., Sun‐Wada, G., Bourgoin, S. G., Casanova, J. E., Wildeman, A. G., Bechoua, S., Ausiello, D. A., et al. (2006) · Nature Cell Biology · doi:10.1038/ncb1348 · Cited by 469 · see citing works

Intracellular Parasite Invasion Strategies

Sibley, L. D. (2004) · Science · doi:10.1126/science.1094717 · Cited by 467 · see citing works

Saccharomyces cerevisiae Fungemia: An Emerging Infectious Disease

Munoz, P., Bouza, E., Cuenca-Estrella, M., Eiros, J. M., Perez, M. J., Sanchez-Somolinos, M., Rincon, C., Hortal, J., & Pelaez, T. (2005) · Clinical Infectious Diseases · doi:10.1086/429916 · Cited by 462 · see citing works

Dendritic cell maturation triggers retrograde MHC class II transport from lysosomes to the plasma membrane

Chow, A. Y., Toomre, D. K., Garrett, W. S., & Mellman, I. (2002) · Nature · doi:10.1038/nature01006 · Cited by 448 · see citing works

Complementation of a Capsule-Deficient Mutation of Cryptococcus neoformans Restores its Virulence

Chang, Y. C., & Kwon-Chung, K. J. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.7.4912-4919.1994 · Cited by 427 · see citing works

T-cell engagement of dendritic cells rapidly rearranges MHC class II transport

Boes, M. L., Černý, J., Massol, R., den Brouw, M. O., Kirchhausen, T. L., Chen, J., & Ploegh, H. L. (2002) · Nature · doi:10.1038/nature01004 · Cited by 416 · see citing works

CD9, CD63, CD81, and CD82 are components of a surface tetraspan network connected to HLA‐DR and VLA integrins

Rubinstein, E., Naour, F. L., Lagaudrière‐Gesbert, C., Billard, M., Conjeaud, H., & Boucheix, C. (1996) · European Journal of Immunology · doi:10.1002/eji.1830261117 · Cited by 366 · see citing works

Replication of <i>Cryptococcus neoformans</i> in macrophages is accompanied by phagosomal permeabilization and accumulation of vesicles containing polysaccharide in the cytoplasm

Tucker, S. C., & Casadevall, A. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.052702799 · Cited by 306 · see citing works

Selective Inhibition of Ii-dependent Antigen Presentation by Helicobacter pylori Toxin VacA

Molinari, M., Salio, M., Galli, C., Norais, N., Rappuoli, R., Lanzavecchia, A., & Montecucco, C. (1998) · The Journal of Experimental Medicine · doi:10.1084/jem.187.1.135 · Cited by 288 · see citing works

Reorganization of multivesicular bodies regulates MHC class II antigen presentation by dendritic cells

Kleijmeer, M. J., Ramm, G., Schuurhuis, D. H., Griffith, J. M., Rescigno, M., Ricciardi‐Castagnoli, P., Rudensky, A. Y., OSSENDORP, F. A., Melief, C. J. M., Stoorvogel, W., et al. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.200103071 · Cited by 288 · see citing works

Studies with a monoclonal antibody against activated platelets: evidence that a secreted 53,000-molecular weight lysosome-like granule protein is exposed on the surface of activated platelets in the circulation

Nieuwenhuis, H. K., van Oosterhout, J., Rozemuller, E. H., van Iwaarden, F., & Sixma, J. J. (1987) · Blood · doi:10.1182/blood.v70.3.838.838 · Cited by 287 · see citing works

Quantitative and Dynamic Assessment of the Contribution of the ER to Phagosome Formation

Touret, N., Paroutis, P., Terebiznik, M. R., Harrison, R. E., Trombetta, S., Pypaert, M., Chow, A. Y., Jiang, A., Shaw, J. E., Yip, C. M., et al. (2005) · Cell · doi:10.1016/j.cell.2005.08.018 · Cited by 285 · see citing works

Retroviral Expression in Embryonic Stem Cells and Hematopoietic Stem Cells

Cherry, S. R., Biniszkiewicz, D., Parijs, L. V., Baltimore, D., & Jaenisch, R. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.20.7419-7426.2000 · Cited by 271 · see citing works

Role of Adaptor Complex AP-3 in Targeting Wild-Type and Mutated CD63 to Lysosomes

Rous, B., Reaves, B. J., Ihrke, G., Briggs, J. A. G., Gray, S. R., Stephens, D. J., Banting, G. S., & Luzio, J. P. (2002) · Molecular Biology of the Cell · doi:10.1091/mbc.01-08-0409 · Cited by 253 · see citing works

<i>Cryptococcus neoformans</i>Resides in an Acidic Phagolysosome of Human Macrophages

Levitz, S. M., Nong, S.-H., Seetoo, K. F., Harrison, T. S., Speizer, R. A., & Simons, E. R. (1999) · Infection and Immunity · doi:10.1128/iai.67.2.885-890.1999 · Cited by 231 · see citing works

Tetraspan microdomains distinct from lipid rafts enrich select peptide–MHC class II complexes

Kropshofer, H., Spindeldreher, S., Röhn, T. A., Platania, N., Grygar, C., Daniel, N., Wolpl, A., Langen, H., Horejsi, V., & Vogt, A. B. (2001) · Nature Immunology · doi:10.1038/ni750 · Cited by 219 · see citing works

Specific interactions among transmembrane 4 superfamily (TM4SF) proteins and phosphoinositide 4-kinase

Yauch, R. L., & Hemler, M. E. (2000) · Biochemical Journal · doi:10.1042/bj3510629 · Cited by 179 · see citing works

The uniformity of phagosome maturation in macrophages

Henry, R. M., Hoppe, A. D., Joshi, N. S., & Swanson, J. A. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200307080 · Cited by 175 · see citing works

The Tetraspan Protein CD82 Is a Resident of MHC Class II Compartments Where It Associates with HLA-DR, -DM, and -DO Molecules

Hammond, C., Denzin, L. K., Pan, M., Griffith, J. M., Geuze, H. J., & Cresswell, P. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.161.7.3282 · Cited by 165 · see citing works

Efficiency of transduction of highly purified murine hematopoietic stem cells by lentiviral and oncoretroviral vectors under conditions of minimal in vitro manipulation.

Mostoslavsky, G., Kotton, D. N., Fabian, A., Gray, J., Lee, J.-S., & Mulligan, R. (2005) · Molecular Therapy · doi:10.1016/j.ymthe.2005.01.005 · Cited by 147 · see citing works

Live Salmonella Modulate Expression of Rab Proteins to Persist in a Specialized Compartment and Escape Transport to Lysosomes

Hashim, S., Mukherjee, K., Raje, M., Basu, S. K., & Mukhopadhyay, A. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.21.16281 · Cited by 145 · see citing works

myo-Inositol 1,4,5-trisphosphate and Ca2+/calmodulin-dependent factors mediate transduction of compression-induced signals in bovine articular chondrocytes

Valhmu, W. B., & Raia, F. J. (2002) · Biochemical Journal · doi:10.1042/0264-6021:3610689 · Cited by 137 · see citing works

Clustering of MHC–peptide complexes prior to their engagement in the immunological synapse: lipid raft and tetraspan microdomains

Vogt, A. B., Spindeldreher, S., & Kropshofer, H. (2002) · Immunological Reviews · doi:10.1034/j.1600-065x.2002.18912.x · Cited by 131 · see citing works

Different fates of phagocytosed particles after delivery into macrophage lysosomes.

Oh, Y., & Swanson, J. A. (1996) · The Journal of Cell Biology · doi:10.1083/jcb.132.4.585 · Cited by 130 · see citing works

CD63 tetraspanin slows down cell migration and translocates to the endosomal-lysosomal-MIICs route after extracellular stimuli in human immature dendritic cells

Mantegazza, A. R., Barrio, M. M., Moutel, S., Bover, L. C., Weck, M. M., Brossart, P., Teillaud, J., & Mordoh, J. (2004) · Blood · doi:10.1182/blood-2004-01-0104 · Cited by 130 · see citing works

Macrophages in host defense against Histoplasma capsulatum

Newman, S. L. (1999) · Trends in Microbiology · doi:10.1016/s0966-842x(98)01431-0 · Cited by 106 · see citing works

Role of Phagocytosis in the Virulence ofCryptococcus neoformans

Poeta, M. D. (2004) · Eukaryotic Cell · doi:10.1128/ec.3.5.1067-1075.2004 · Cited by 100 · see citing works

Association of distinct tetraspanins with MHC class II molecules at different subcellular locations in human immature dendritic cells

Engering, A. J., & Pieters, J. (2001) · International Immunology · doi:10.1093/intimm/13.2.127 · Cited by 96 · see citing works

CD63 modulates spreading and tyrosine phosphorylation of platelets on immobilized fibrinogen

McMillan‐Ward, E., & Israels, S. J. (2005) · Thrombosis and Haemostasis · doi:10.1160/th04-08-0503 · Cited by 63 · see citing works

The shared tumor-specific antigen encoded by mouse geneP1A is a target not only for cytolytic T lymphocytes but also for tumor rejection

Brändle, D., Bilsborough, J., Rülicke, T., Uyttenhove, C., Boon, T., & den Eynde, B. J. V. (1998) · European Journal of Immunology · doi:10.1002/(sici)1521-4141(199812)28:12 · Cited by 62 · see citing works

Differential post‐translational modification of CD63 molecules during maturation of human dendritic cells

Engering, A. J., Kuhn, L., Fluitsma, D. M., Hoefsmit, E. C. M., & Pieters, J. (2003) · European Journal of Biochemistry · doi:10.1046/j.1432-1033.2003.03609.x · Cited by 55 · see citing works

Trafficking and function of the tetraspanin CD63

Pols, M. S., & Klumperman, J. (2009) · Experimental Cell Research · doi:10.1016/j.yexcr.2008.09.020 · Cited by 745 · see citing works

The known unknowns of antigen processing and presentation

Vyas, J., van der Veen, A. G., & Ploegh, H. (2008) · Nature reviews. Immunology · doi:10.1038/nri2368 · Cited by 703 · see citing works

Interactions of fungal pathogens with phagocytes

Erwig, L. P., & Gow, N. A. R. (2016) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2015.21 · Cited by 626 · see citing works

miR-200–containing extracellular vesicles promote breast cancer cell metastasis

Le, M. T. N., Hamar, P., Guo, C., Basar, E., Perdigão-Henriques, R., Balaj, L., & Lieberman, J. (2014) · Journal of Clinical Investigation · doi:10.1172/jci75695 · Cited by 450 · see citing works

Tubulation of Class II MHC Compartments Is Microtubule Dependent and Involves Multiple Endolysosomal Membrane Proteins in Primary Dendritic Cells

Vyas, J. M., Kim, Y., Artavanis‐Tsakonas, K., Love, J. C., van der Veen, A. G., & Ploegh, H. L. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.11.7199 · Cited by 146 · see citing works

Cryptococcus interactions with macrophages: evasion and manipulation of the phagosome by a fungal pathogen

Johnston, S. A., & May, R. C. (2012) · Cellular Microbiology · doi:10.1111/cmi.12067 · Cited by 145 · see citing works

Corticosteroids Block Autophagy Protein Recruitment in <i>Aspergillus fumigatus</i> Phagosomes via Targeting Dectin-1/Syk Kinase Signaling

Kyrmizi, I., Gresnigt, M. S., Akoumianaki, T., Samonis, G., Sidiropoulos, P., Boumpas, D., Netea, M. G., van de Veerdonk, F. L., Kontoyiannis, D. P., & Chamilos, G. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1300132 · Cited by 142 · see citing works

Cryptococcus neoformans: historical curiosity to modern pathogen

Srikanta, D., Santiago-Tirado, F. H., & Doering, T. L. (2013) · Yeast · doi:10.1002/yea.2997 · Cited by 140 · see citing works

Tetraspanin CD63 Bridges Autophagic and Endosomal Processes To Regulate Exosomal Secretion and Intracellular Signaling of Epstein-Barr Virus LMP1

Hurwitz, S. N., Cheerathodi, M. R., Nkosi, D., York, S. B., & Meckes, D. G. (2017) · Journal of Virology · doi:10.1128/jvi.01969-17 · Cited by 141 · see citing works

Cryptococcus neoformans urease affects the outcome of intracellular pathogenesis by modulating phagolysosomal pH

Fu, M. S., Coelho, C., De Leon-Rodriguez, C. M., Rossi, D. C. P., Camacho, E., Jung, E. H., Kulkarni, M., & Casadevall, A. (2018) · PLOS Pathogens · doi:10.1371/journal.ppat.1007144 · Cited by 138 · see citing works

The Intracellular Life ofCryptococcus neoformans

Coelho, C., Bocca, A. L., & Casadevall, A. (2013) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathol-012513-104653 · Cited by 130 · see citing works

Exosomes derived from neural progenitor cells preserve photoreceptors during retinal degeneration by inactivating microglia

Bian, B., Zhao, C., He, X.-Y., Gong, Y., Ren, C., Ge, L., Zeng, Y., Li, Q., Chen, M., Weng, C., et al. (2020) · Journal of Extracellular Vesicles · doi:10.1080/20013078.2020.1748931 · Cited by 125 · see citing works

The ancestry and cumulative evolution of immune reactions.

Dzik, J. (2010) · Acta Biochimica Polonica · doi:10.18388/abp.2010_2431 · Cited by 123 · see citing works

Cryptococcus and Phagocytes: Complex Interactions that Influence Disease Outcome

Wager, C. M. L., Hole, C. R., Wozniak, K. L., & Wormley, F. L. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00105 · Cited by 103 · see citing works

Functional Analysis of Host Factors that Mediate the Intracellular Lifestyle of Cryptococcus neoformans

Qin, Q., Luo, J., Lin, X., Pei, J., Li, L., Ficht, T. A., & de Figueiredo, P. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1002078 · Cited by 101 · see citing works

Dectin-1–Dependent LC3 Recruitment to Phagosomes Enhances Fungicidal Activity in Macrophages

Tam, J. M., Mansour, M. K., Khan, N. S., Seward, M., Puranam, S., Tanne, A., Sokolovska, A., Becker, C. E., Acharya, M., Baird, M. A., et al. (2014) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiu290 · Cited by 101 · see citing works

The Tools for Virulence of Cryptococcus neoformans

Coelho, C., Bocca, A. L., & Casadevall, A. (2014) · Advances in applied microbiology · doi:10.1016/b978-0-12-800261-2.00001-3 · Cited by 98 · see citing works

The fungal pathogenCryptococcus neoformansmanipulates macrophage phagosome maturation

Taylor-Smith, L. M., Dixon, E. F., & May, R. C. (2014) · Cellular Microbiology · doi:10.1111/cmi.12394 · Cited by 98 · see citing works

Dectin-1 Activation Controls Maturation of β-1,3-Glucan-containing Phagosomes

Mansour, M. K., Tam, J. M., Khan, N. S., Seward, M., Davids, P. J., Puranam, S., Sokolovska, A., Sykes, D. B., Dagher, Z., Becker, C., et al. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.473223 · Cited by 85 · see citing works

Tetraspanins - Gateways for Infection

Monk, P. N., & Partridge, L. J. (2012) · Infectious Disorders - Drug Targets · doi:10.2174/187152612798994957 · Cited by 84 · see citing works

Cryptococcus neoformans–Induced Macrophage Lysosome Damage Crucially Contributes to Fungal Virulence

Davis, M. J., Eastman, A. J., Qiu, Y., Gregorka, B., Kozel, T. R., Osterholzer, J. J., Curtis, J. L., Swanson, J. A., & Olszewski, M. A. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402376 · Cited by 80 · see citing works

Palmitoylation-dependent association with CD63 targets the Ca2+ sensor synaptotagmin VII to lysosomes

Flannery, A. R., Czibener, C., & Andrews, N. W. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201003021 · Cited by 79 · see citing works

Cryptococcus neoformansEnters the Endolysosomal Pathway of Dendritic Cells and Is Killed by Lysosomal Components

Wozniak, K. L., & Levitz, S. M. (2008) · Infection and Immunity · doi:10.1128/iai.00660-08 · Cited by 79 · see citing works

Mechanisms of microbial escape from phagocyte killing

Taylor-Smith, L. M., & May, R. C. (2013) · Biochemical Society Transactions · doi:10.1042/bst20130014 · Cited by 76 · see citing works

Genome-wide transcriptional changes induced by phagocytosis or growth on bacteria in Dictyostelium

Sillo, A., Bloomfield, G., Balest, A., Balbo, A., Pergolizzi, B., Peracino, B., Skelton, J., Ivens, A., & Bozzaro, S. (2008) · BMC Genomics · doi:10.1186/1471-2164-9-291 · Cited by 69 · see citing works

Toll-Like Receptor 9 Modulates Macrophage Antifungal Effector Function during Innate Recognition of Candida albicans and Saccharomyces cerevisiae

Kasperkovitz, P. V., Khan, N. S., Tam, J. M., Mansour, M. K., Davids, P. J., & Vyas, J. M. (2011) · Infection and Immunity · doi:10.1128/iai.05626-11 · Cited by 59 · see citing works

Tetraspanins as Organizers of Antigen-Presenting Cell Function

Sáiz, M. L., Rocha‐Perugini, V., & Sánchez‐Madrid, F. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01074 · Cited by 55 · see citing works

Characterization of tetraspanins CD9, CD53, CD63, and CD81 in monocytes and macrophages in HIV-1 infection

Tippett, E., Cameron, P. U., Marsh, M., & Crowe, S. M. (2013) · Journal of Leukocyte Biology · doi:10.1189/jlb.0812391 · Cited by 53 · see citing works

Cryptococcus neoformans: Tripping on Acid in the Phagolysosome

DeLeon‐Rodriguez, C. M., & Casadevall, A. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00164 · Cited by 48 · see citing works

Fungal killing by mammalian phagocytic cells

Nicola, A. M., Casadevall, A., & Goldman, D. L. (2008) · Current Opinion in Microbiology · doi:10.1016/j.mib.2008.05.011 · Cited by 46 · see citing works

Function and Dynamics of Tetraspanins during Antigen Recognition and Immunological Synapse Formation

Rocha‐Perugini, V., Sánchez‐Madrid, F., & del Hoyo, G. M. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00653 · Cited by 45 · see citing works

Macrophages use a bet-hedging strategy for antimicrobial activity in phagolysosomal acidification

Dragotakes, Q., Stouffer, K. M., Fu, M. S., Sella, Y., Youn, C., Yoon, O. I., Leon-Rodriguez, C. M. D., Freij, J. B., Bergman, A., & Casadevall, A. (2020) · Journal of Clinical Investigation · doi:10.1172/jci133938 · Cited by 40 · see citing works

The Tetraspanin CD82 Is Specifically Recruited to Fungal and Bacterial Phagosomes prior to Acidification

Artavanis‐Tsakonas, K., Kasperkovitz, P. V., Papa, E., Cardenas, M., Khan, N. S., van der Veen, A. G., Ploegh, H. L., & Vyas, J. M. (2010) · Infection and Immunity · doi:10.1128/iai.01135-10 · Cited by 38 · see citing works

Use of fungal derived polysaccharide-conjugated particles to probe Dectin-1 responses in innate immunity

Tam, J. M., Mansour, M. K., Khan, N. S., Yoder, N. C., & Vyas, J. M. (2011) · Integrative Biology · doi:10.1039/c2ib00089j · Cited by 34 · see citing works

Tetraspanin CD82 Organizes Dectin-1 into Signaling Domains to Mediate Cellular Responses to Candida albicans

Tam, J. M., Reedy, J. L., Lukason, D. P., Kuna, S. G., Acharya, M., Khan, N. S., Negoro, P. E., Xu, S., Ward, R., Feldman, M. B., et al. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1801384 · Cited by 31 · see citing works

Immunoglobulin G signaling activates lysosome/phagosome docking

Trivedi, V., Zhang, S. C., Castoreno, A. B., Stockinger, W., Shieh, E. C., Vyas, J. M., Frickel, E., & Nohturfft, A. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0609182103 · Cited by 31 · see citing works

Differential recruitment of CD63 and Rab7-interacting-lysosomal-protein to phagosomes containingMycobacterium tuberculosisin macrophages

Seto, S., Matsumoto, S., Tsujimura, K., & Koide, Y. (2010) · Microbiology and Immunology · doi:10.1111/j.1348-0421.2010.00199.x · Cited by 25 · see citing works

Control and Manipulation of Pathogens with an Optical Trap for Live Cell Imaging of Intercellular Interactions

Tam, J. M., Castro, C. E., Heath, R. J. W., Cardenas, M., Xavier, R. J., Lang, M. J., & Vyas, J. M. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015215 · Cited by 25 · see citing works

Macrophage–Cryptococcus Interactions: An Update

Mansour, M. K., Reedy, J. L., Tam, J. M., & Vyas, J. M. (2013) · Current Fungal Infection Reports · doi:10.1007/s12281-013-0165-7 · Cited by 23 · see citing works

The cell biology of the innate immune response to Aspergillus fumigatus

Mansour, M. K., Tam, J. M., & Vyas, J. M. (2012) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2012.06837.x · Cited by 20 · see citing works

Interactions of Cryptococcus with Dendritic Cells

Wozniak, K. L. (2018) · Journal of Fungi · doi:10.3390/jof4010036 · Cited by 20 · see citing works

Molecular Cloning, Sequence Characterization and Expression Analysis of a CD63 Homologue from the Coleopteran Beetle, Tenebrio molitor

Patnaik, B. B., Kang, S. J., Seo, G. W., Lee, H., Patnaik, H. H., Jo, Y. H., Tindwa, H. J., Lee, Y. S., Lee, B. L., Kim, N., et al. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms141020744 · Cited by 16 · see citing works

Vomocytosis: Too Much Booze, Base, or Calcium?

Cruz‐Acuña, M., Pacifici, N. J., & Lewis, J. S. (2019) · mBio · doi:10.1128/mbio.02526-19 · Cited by 12 · see citing works

Efficient phagosomal maturation and degradation of Plasmodium-infected erythrocytes by dendritic cells and macrophages

Bettiol, E., van de Hoef, D. L., Carapau, D., & Rodrı́guez, A. (2010) · Parasite Immunology · doi:10.1111/j.1365-3024.2010.01198.x · Cited by 13 · see citing works

Vomocytosis of Cryptococcus neoformans cells from murine, bone marrow-derived dendritic cells

Pacifici, N. J., Cruz‐Acuña, M., Diener, A., Tu, A. B., Senthil, N., Han, H., & Lewis, J. S. (2023) · PLoS ONE · doi:10.1371/journal.pone.0280692 · Cited by 11 · see citing works

A CD63 Homolog Specially Recruited to the Fungi-Contained Phagosomes Is Involved in the Cellular Immune Response of Oyster Crassostrea gigas

Liu, C., Yang, C., Wang, M., Jiang, S., Yi, Q., Wang, W., Wang, L., & Song, L. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01379 · Cited by 10 · see citing works

Inflammation-targeting and self-limited neutrophilic membrane-encapsulated teicoplanin for the treatment of infectious pneumonia

Lu, H., Zhang, K., Zhang, W., Zhang, W., Wu, J., Ming, X., Huang, Y., Xu, F., & Wang, B. (2025) · Trends in biotechnology · doi:10.1016/j.tibtech.2025.05.009 · Cited by 9 · see citing works

Innate Pulmonary Phagocytes and Their Interactions with Pathogenic Cryptococcus Species

Conn, B. N., & Wozniak, K. L. (2023) · Journal of Fungi · doi:10.3390/jof9060617 · Cited by 8 · see citing works

Cholesterol Levels and Monocyte Phenotype Are Predictors of Nonhealing in Individuals with Low-Grade Diabetic Foot Ulcers: A Prospective Cohort Study

Raghavan, J. V., Sagar, S. K., Dorai, V. K., Samuel, R., Arunachalam, P., Chaluvanarayana, H. C., Belahalli, P., Kalpana, S., & Jhunjhunwala, S. (2022) · Advances in Wound Care · doi:10.1089/wound.2021.0182 · Cited by 8 · see citing works

Differential recruitment of CD63 and Rab7-interacting-lysosomal-protein to phagosomes containing Mycobacterium tuberculosis in macrophages

Seto, S., Matsumoto, S., Tsujimura, K., & Koide, Y. (2009) · Microbiology and Immunology · doi:10.1111/j.1348-0421.2009.00199.x · Cited by 7 · see citing works

Dendritic Cells: Multifunctional Roles in Host Defenses to Cryptococcus Infections

Goughenour, K. D., Nair, A. S., Xu, J., Olszewski, M. A., & Wozniak, K. L. (2023) · Journal of Fungi · doi:10.3390/jof9111050 · Cited by 6 · see citing works

Deacidification of the Endolysosomal System by the Vesicular Proton Pump V-ATPase Inhibitor Bafilomycin A1 Affects EGF Receptor Endocytosis Differently in Endometrial MSC and HeLa Cells

Salova, A. V., Belyaeva, T. N., Litvinov, I. K., Харченко, М. В., & Корнилова, Е. С. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262010226 · Cited by 3 · see citing works

Anti-human CD63 monoclonal antibody COS3A upregulates monocyte-induced IL-10 excretion leading to diminution of CD3-mediated T cell response

Wansook, S., Mahasongkram, K., Chruekamlow, N., Pata, S., Kasinrerk, W., & Khunkaewla, P. (2019) · Molecular Immunology · doi:10.1016/j.molimm.2019.09.005 · Cited by 2 · see citing works

Insights into dendritic cell function using advanced imaging modalities

Vyas, J. M. (2012) · Virulence · doi:10.4161/viru.22981 · Cited by 3 · see citing works

Luminal decoration of blood vessels by activated perivasal mast cells in allergic rhinitis

Schaefer, T., Zajonz, A., Lorentz, P., Bohnacker, T., Wymann, M. P., & Schweighoffer, T. (2012) · Allergy · doi:10.1111/j.1398-9995.2012.02790.x · Cited by 3 · see citing works

Biochemical and functional analysis of COS3A, a novel CD63-specific monoclonal antibody

Wansook, S., Pata, S., Kasinrerk, W., & Khunkaewla, P. (2016) · Asian Pacific Journal of Allergy and Immunology · doi:10.12932/ap0735 · Cited by 2 · see citing works

Host–Pathogen Interactions and Correlated Factors That Are Affected in Replicative-Aged Cryptococcus neoformans

Silva, V. K. A., Min, S., Yoo, K., & Fries, B. C. (2024) · Journal of Fungi · doi:10.3390/jof10040279 · Cited by 1 · see citing works

Tetraspanins and Immunity

Wright, M. D., & Levy, S. (2013) · Springer eBooks · doi:10.1007/978-94-007-6070-7_10 · Cited by 1 · see citing works

Microreview Cryptococcus interactions with macrophages: evasion and manipulation of the phagosome by a fungal pathogen

Johnston, S. A., & May, R. C. (2013) · Cited by 1 · see citing works

Faculty Opinions recommendation of Palmitoylation-dependent association with CD63 targets the Ca2+ sensor synaptotagmin VII to lysosomes.

Klumperman, J. (2010) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.6609956.6749054

Vomocytosis of Cryptococcus neoformans cells from murine, bone marrow-derived dendritic cellsPreprint

Pacifici, N. J., Cruz‐Acuña, M., Diener, A., Senthil, N., Han, H., & Lewis, J. S. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.28.486165

Lipid Flippase Mediated Membrane Asymmetry Governs Extracellular Vesicles Biogenesis and Host Interactions in Cryptococcus neoformansPreprint

Pawar, S., Zhnag, Y., Varsanyi, C., Gadiyar, V., Avina, S. L., Birge, R. B., & Xue, C. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.12.731820

The Tetraspanin CD82 Is Specifically Recruited to Fungal and Bacterial Phagosomes prior to Acidification

Artavanis‐Tsakonas, K., Kasperkovitz, P. V., Papa, E., Cardenas, M., Khan, N. S., van der Veen, A. G., Ploegh, H. L., & Vyas, J. M. (2010) · Infection and Immunity · doi:10.1128/iai.01135-10 · Cited by 38 · see citing works

Real-time visualization of phagosomal pH manipulation by Cryptococcus neoformans in an immune signal-dependent way

Santiago-Burgos, E. J., Stuckey, P. V., & Santiago-Tirado, F. H. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.967486 · Cited by 11 · see citing works

<i>Cryptococcus neoformans</i>Resides in an Acidic Phagolysosome of Human Macrophages

Levitz, S. M., Nong, S.-H., Seetoo, K. F., Harrison, T. S., Speizer, R. A., & Simons, E. R. (1999) · Infection and Immunity · doi:10.1128/iai.67.2.885-890.1999 · Cited by 231 · see citing works

Interactions between fungal hyaluronic acid and host CD44 promote internalization by recruiting host autophagy proteins to forming phagosomes

Ding, S., Yang, J. H., Feng, X., Pandey, A., Barhoumi, R., Zhang, D., Bell, S. L., Liu, Y., da Costa, L. F., Rice‐Ficht, A. C., et al. (2021) · iScience · doi:10.1016/j.isci.2021.102192 · Cited by 9 · see citing works

The Capsule of Cryptococcus neoformans Modulates Phagosomal pH through Its Acid-Base Properties

Leon-Rodriguez, C. M. D., Fu, M. S., Corbali, O., Cordero, R. J. B., & Casadevall, A. (2018) · mSphere · doi:10.1128/msphere.00437-18 · Cited by 63 · see citing works