CD81 Regulates Neuron-Induced Astrocyte Cell-Cycle Exit

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

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The tetraspanin superfamily: molecular facilitators

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Rapid, widespread, and longlasting induction of nestin contributes to the generation of glial scar tissue after CNS injury.

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Characterization of Hepatitis C Virus E2 Glycoprotein Interaction with a Putative Cellular Receptor, CD81

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Riding the glial monorail: A common mechanism for glialguided neuronal migration in different regions of the developing mammalian brain

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Fibrillary astrocytes proliferate in response to brain injury

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Initial tract formation in the mouse brain

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QUANTITATIVE ANALYSIS OF CELL PROLIFERATION AND DIFFERENTIATION IN THE CORTEX OF THE POSTNATAL MOUSE CEREBELLUM

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Suppression by antisense mRNA demonstrates a requirement for the glial fibrillary acidic protein in the formation of stable astrocytic processes in response to neurons.

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Normal Lymphocyte Development but Delayed Humoral Immune Response in CD81-null Mice

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Normal development but differentially altered proliferative responses of lymphocytes in mice lacking CD81

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Astrotactin: a novel neuronal cell surface antigen that mediates neuron-astroglial interactions in cerebellar microcultures

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Impaired CD19 expression and signaling, enhanced antibody response to type II T independent antigen and reduction of B-1 cells in CD81-deficient mice

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A Neural Tetraspanin, Encoded by late bloomer , That Facilitates Synapse Formation

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Astroglial cells provide a template for the positioning of developing cerebellar neurons in vitro.

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A Role for CD81 in Early T Cell Development

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CD81 on B cells promotes interleukin 4 secretion and antibody production during T helper type 2 immune responses

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Antibodies that recognize astrotactin block granule neuron binding to astroglia

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Histogenesis of the anterior limb of the anterior commissure of the mouse brain. 3. An electron microscopic study of gliogenesis.

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Astrocyte Growth, Reactivity, and the Target of the Antiproliferative Antibody, TAPA

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Oxystdrol (7β‐hydroxycholestesteryl‐3‐oleate) promotes serotonergic reinnervation in the lesioned rat spinal cord by reducing glial reaction

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Astrocyte Progression from G1 to S Phase of the Cell Cycle Depends upon Multiple Protein Interaction

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Differential Regulation of Cyclin D1 and D3 Expression in the Control of Astrocyte Proliferation Induced by Endothelin‐1

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Histogenesis of the anterior limb of the anterior commissure of the mouse brain. I. A quantitative study of changes in the glial population with age.

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Differential Expression of Murine CD81 Highlighted by New Anti-Mouse CD81 Monoclonal Antibodies

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Mouse cerebellar granule neurons arrest the proliferation of human and rodent astrocytoma cells in vitro

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Neuron–Astroglial Interactions In Vitro and Their Implications for Repair of CNS Injury

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Histogenesis of the anterior limb of the anterior commissure of the mouse brain. II. A quantitative study of pre- and postnatal mitosis.

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C17, a retrovirally immortalized neuronal cell line, inhibits the proliferation of astrocytes and astrocytoma cells by a contact‐mediated mechanism

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Tetraspanin Proteins Mediate Cellular Penetration, Invasion, and Fusion Events and Define a Novel Type of Membrane Microdomain

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Lateral organization of membrane proteins: tetraspanins spin their web

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Specific tetraspanin functions

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CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency

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Mesenchymal stem cell-derived exosomes as a nanotherapeutic agent for amelioration of inflammation-induced astrocyte alterations in mice

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Hepatocyte CD81 is required for Plasmodium falciparum and Plasmodium yoelii sporozoite infectivity

Silvie, O., Rubinstein, E., Franetich, J., Prenant, M., Belnoue, E., Rénia, L., Hannoun, L., Eling, W. M. C., Levy, S., Boucheix, C., et al. (2002) · Nature Medicine · doi:10.1038/nm808 · Cited by 351 · see citing works

Evolution of increased glia–neuron ratios in the human frontal cortex

Sherwood, C. C., Stimpson, C. D., Raghanti, M. A., Wildman, D. E., Uddin, M., Grossman, L. I., Goodman, M., Redmond, J. C., Bonar, C. J., Erwin, J. M., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605843103 · Cited by 342 · see citing works

EWI-2 Is a Major CD9 and CD81 Partner and Member of a Novel Ig Protein Subfamily

Stipp, C. S., Kolesnikova, T. V., & Hemler, M. E. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m107338200 · Cited by 233 · see citing works

Reduced fertility of female mice lacking CD81

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Tetraspanins CD9 and CD81 function to prevent the fusion of mononuclear phagocytes

Takeda, Y., Tachibana, I., Miyado, K., Kobayashi, M., Miyazaki, T., Funakoshi, T., Kimura, H., Yamane, H., Saito, Y., Goto, H., et al. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200212031 · Cited by 199 · see citing works

Characterization of Mice Lacking the Tetraspanin Superfamily Member CD151

Wright, M. D., Geary, S. M., Fitter, S., Moseley, G. W., Lau, L.-M., Sheng, K., Apostolopoulos, V., Stanley, E. G., Jackson, D. E., & Ashman, L. K. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.13.5978-5988.2004 · Cited by 173 · see citing works

Role of Integrins in the Development of the Cerebral Cortex

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The Tetraspanin CD81 Regulates the Expression of CD19 During B Cell Development in a Postendoplasmic Reticulum Compartment

Shoham, T., Rajapaksa, R., Boucheix, C., Rubinstein, E., Poe, J. C., Tedder, T. F., & Levy, S. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.8.4062 · Cited by 127 · see citing works

Residues SFQ (173-175) in the large extracellular loop of CD9 are required for gamete fusion

Zhu, G., Miller, B. J., Boucheix, C., Rubinstein, E., Liu, C. C., Hynes, R. O., Myles, D. G., & Primakoff, P. (2002) · Development · doi:10.1242/dev.129.8.1995 · Cited by 125 · see citing works

None of the integrins known to be present on the mouse egg or to be ADAM receptors are essential for sperm–egg binding and fusion

He, Z.-Y., Brakebusch, C., Fässler, R., Kreidberg, J. A., Primakoff, P., & Myles, D. G. (2003) · Developmental Biology · doi:10.1016/s0012-1606(02)00043-x · Cited by 118 · see citing works

Tetraspanins: Interactions and interplay with integrins

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Controlling cell surface dynamics and signaling: How CD82/KAI1 suppresses metastasis

Miranti, C. K. (2008) · Cellular Signalling · doi:10.1016/j.cellsig.2008.08.023 · Cited by 100 · see citing works

Candidate genes, pathways and mechanisms for alcoholism: an expanded convergent functional genomics approach

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Increased brain size and glial cell number in CD81‐null mice

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Mesenchymal stem cell-derived extracellular vesicles attenuate tPA-induced blood–brain barrier disruption in murine ischemic stroke models

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Critical role of CD81 in cognate T–B cell interactions leading to Th2 responses

Deng, J., DeKruyff, R. H., Freeman, G. J., Umetsu, D. T., & Levy, S. (2002) · International Immunology · doi:10.1093/intimm/14.5.513 · Cited by 72 · see citing works

Genomewide analysis of the Drosophila tetraspanins reveals a subset with similar function in the formation of the embryonic synapse

Fradkin, L., Kamphorst, J., Diantonio, A., Goodman, C., & Noordermeer, J. N. (2002) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.212511099 · Cited by 80 · see citing works

Alternative invasion pathways for plasmodium berghei sporozoites

Silvie, O., Franetich, J., Boucheix, C., Rubinstein, E., & Mazier, D. (2006) · International Journal for Parasitology · doi:10.1016/j.ijpara.2006.10.005 · Cited by 62 · see citing works

In vivo gene silencing of CD81 by lentiviral expression of small interference RNAs suppresses cocaine‐induced behaviour

Bahí, A., Boyer, F., Kolira, M., & Dreyer, J. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02961.x · Cited by 60 · see citing works

CD81 Is Essential for the Re-entry of Hematopoietic Stem Cells to Quiescence following Stress-Induced Proliferation Via Deactivation of the Akt Pathway

Lin, K. K., Rossi, L., Boles, N. C., Hall, B. E., George, T. C., & Goodell, M. A. (2011) · PLoS Biology · doi:10.1371/journal.pbio.1001148 · Cited by 59 · see citing works

Glioblastoma Inhibition by Cell Surface Immunoglobulin Protein EWI-2, In Vitro and In Vivo

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CD9 inhibition reveals a functional connection of extracellular vesicle secretion with mitophagy in melanoma cells

Suárez, H., Andreu, Z., Mazzeo, C., Toribio, V., Pérez‐Rivera, A. E., López‐Martín, S., Garcı́a-Silva, S., Hurtado, B., Morato, E., Peláez, L., et al. (2021) · Journal of Extracellular Vesicles · doi:10.1002/jev2.12082 · Cited by 52 · see citing works

Gene expression changes after seizure preconditioning in the three major hippocampal cell layers

Borges, K., Shaw, R. N., & Dingledine, R. J. (2007) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.12.001 · Cited by 42 · see citing works

Synthesis of 1-Boraadamantaneamine Derivatives with Selective Astrocyte vs C6 Glioma Antiproliferative Activity. A Novel Class of Anti-Hepatitis C Agents with Potential to Bind CD81

Wagner, C. E., Mohler, M. L., Kang, G. S., Miller, D. D., Geisert, E. E., Chang, Y.-A., Fleischer, E. B., & Shea, K. J. (2003) · Journal of Medicinal Chemistry · doi:10.1021/jm020326d · Cited by 27 · see citing works

CD81, a cell cycle regulator, is a novel target for histone deacetylase inhibition in glioma cells

Gensert, J. M., Baranova, O. V., Weinstein, D. E., & Ratan, R. R. (2007) · Neurobiology of Disease · doi:10.1016/j.nbd.2007.03.008 · Cited by 23 · see citing works

Tetraspanin CD81 regulates HSV-1 infection

Benayas, B., Sastre, I., López‐Martín, S., Oo, A., Kim, B., Bullido, M. J., Aldudo, J., & Yáñez‐Mó, M. (2020) · Medical Microbiology and Immunology · doi:10.1007/s00430-020-00684-0 · Cited by 22 · see citing works

IgSF8: A developmentally and functionally regulated cell adhesion molecule in olfactory sensory neuron axons and synapses

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Exosomes encapsulated in hydrogels for effective central nervous system drug delivery

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Normal viability of Kai1/Cd82 deficient mice

Risinger, J. I., Custer, M. C., Feigenbaum, L., Simpson, R. J., Hoover, S. B., Webster, J. D., Chandramouli, G. V. R., Tessarollo, L., & Barrett, J. C. (2013) · Molecular Carcinogenesis · doi:10.1002/mc.22009 · Cited by 18 · see citing works

Increased density of retinal pigment epithelium in cd81−/− mice

Song, B. K., Levy, S., & Geisert, E. E. (2004) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20145 · Cited by 13 · see citing works

Genomic organization and embryonic expression of igsf8, an immunoglobulin superfamily member implicated in development of the nervous system and organ epithelia

Murdoch, J. N., Doudney, K., Gerrelli, D., Wortham, N. C., Paternotte, C., Stanier, P., & Copp, A. J. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(02)00021-0 · Cited by 12 · see citing works

CD81 inhibits the proliferation of astrocytes by inducing G0/G1 arrest in vitro

Ma, J., Liu, R., Peng, H., Zhou, J.-P., & Li, H. (2010) · Journal of Huazhong University of Science and Technology [Medical Sciences] · doi:10.1007/s11596-010-0214-1 · Cited by 12 · see citing works

Macrophage cell lines use CD81 in cell growth regulation

Mordica, W. J., Woods, K. M., Clem, R. J., Passarelli, A. L., & Chapes, S. K. (2009) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-008-9167-0 · Cited by 12 · see citing works

Persistent type I interferon signaling within the brain of people with HIV on ART with cognitive impairment

Tang, Y., Xie, L., Shabangu, C. S., Li, D., Prates, G. D. S., Ashokkumar, M., Wong, L., Chaillon, A., Browne, E. P., Gianella, S., et al. (2025) · PLoS Pathogens · doi:10.1371/journal.ppat.1013411 · Cited by 11 · see citing works

Therapeutic targeting of membrane-associated proteins in central nervous system tumors

Roy, P., Rajesh, Y., & Mandal, M. (2021) · Experimental Cell Research · doi:10.1016/j.yexcr.2021.112760 · Cited by 10 · see citing works

The Effect of Intravenous Injection of the Water Extract of Angelica gigas Nakai on Gliosis in the Middle Cerebral Artery Occlusion Rats

Song, B.-K., Jeon, Y.-C., Kim, S.-A., Shim, A.-N., Seong, K., & Lee, E.-J. (2011) · Journal of pharmacopuncture · doi:10.3831/kpi.2011.14.3.005 · Cited by 9 · see citing works

Tsp66E, the Drosophila KAI1 homologue, and Tsp74F function to regulate ovarian follicle cell and wing development by stabilizing integrin localization

Han, S. Y., Lee, M., Hong, Y. K., Hwang, S., Choi, G., Suh, Y. S., Park, S. H., Lee, S., Lee, S., Chung, J., et al. (2012) · FEBS Letters · doi:10.1016/j.febslet.2012.09.044 · Cited by 9 · see citing works

CD81 Promotes a Migratory Phenotype in Neuronal-Like Cells

Martins, S., Correia, P. D., Dias, R. A., Silva, O. A. B. D. C. E., & Vieira, S. I. (2019) · Microscopy and Microanalysis · doi:10.1017/s1431927618015532 · Cited by 8 · see citing works

The Role of Tetraspanin Complexes in Egg-Sperm Fusion

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The Effects of a Cd81 Null Mutation on Retinal Pigment Epithelium in Mice

Pan, Y., Geisert, D. F., Orr, W. E., & Geisert, E. E. (2010) · Neurochemical Research · doi:10.1007/s11064-010-0268-2 · Cited by 6 · see citing works

The Tetraspanin CD9 Localizes to Platelet-Platelet Contacts and Regulates Thrombus Stability

Hill, S. (2008) · doi:10.21007/etd.cghs.2008.0138 · Cited by 5 · see citing works

The CD63 homologs, Tsp42Ee and Tsp42Eg, restrict endocytosis and promote neurotransmission through differential regulation of synaptic vesicle pools

Hendricks, E. L., Smith, I. R., Prates, B., Lighvan, F. B., & Liebl, F. L. W. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.957232 · Cited by 3 · see citing works

Decision tree insights analytics (DTIA) tool: an analytic framework to identify insights from large data records across fields of science

Hossny, K., Hossny, M., Cougnoux, A., Mahmoud, L., & Villanueva, W. (2024) · Machine Learning Science and Technology · doi:10.1088/2632-2153/ad7f23 · Cited by 3 · see citing works

Regulation of cell cycle progression in astrocytes

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The Cell Subtypes Selection by Genes (CSSG) algorithm for discovering cell populations in high resolutionPreprint

Kubiś, J., & Figiel, M. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.20.537649 · Cited by 3 · see citing works

Targeted surface marker screening on neuronal structures in the human choroid

Wolfmeier, H., Heindl, S., Platzl, C., Kaser-Eichberger, A., Nematian-Ardestani, E., Strohmaier, C., Pruszak, J., & Schroedl, F. (2022) · Experimental Eye Research · doi:10.1016/j.exer.2022.109368 · Cited by 2 · see citing works

Application of Thermodynamics and Protein–Protein Interaction Network Topology for Discovery of Potential New Treatments for Temporal Lobe Epilepsy

Yu, C., Rietman, E. A., Siegelmann, H. T., Cavaglià, M., & Tuszyński, J. A. (2021) · Applied Sciences · doi:10.3390/app11178059 · Cited by 2 · see citing works

Pulmonary Manifestations of Predominantly Antibody Deficiencies

Saghazadeh, A., & Rezaei, N. (2018) · Springer eBooks · doi:10.1007/978-3-030-00880-2_3 · Cited by 1 · see citing works

Genetic Evidence for Tetraspanin Functions

Hemler, M. E. (2013) · Springer eBooks · doi:10.1007/978-94-007-6070-7_7 · Cited by 1 · see citing works

Can exosomes be used as drug delivery vesicles

Cooke, F. G. M. (2018) · St Andrews Research Repository (St Andrews Research Repository)

CD81

Levy, S. (2010) · AfCS-Nature Molecule Pages · doi:10.1038/mp.a000591.01

Unraveling the function of tetraspanin CD81 and its cognate adhesins from Mycobacterium abscessus during host cell invasion

Karam, J. (2022) · theses.fr (ABES) · doi:10.70675/db77032az1c53z4fa3za2f9z7ccd9985f01d

Functional impacts of Huntingtin lowering on the synaptic maturation and activity of neuronal networks derived from human induced pluripotent stem cells

Louçã, M. (2024) · theses.fr (ABES) · doi:10.70675/f5800d08zd8f4z4fbdz9043za4bde4fa031a

Yin Yang 1 Specifically Supports the Development of Olig2 Positive Cerebellar Astrocytes

Zarei‐Kheirabadi, M., Tyc, K. M., Dain, L., Kheirabadi, M. A., Hanco, J., Mockenhaupt, K., Munir, S., McQuiston, A. R., Singh, S. K., & Kordula, T. (2026) · Glia · doi:10.1002/glia.70185

Pervasive Somatic Mutations in NF1 Drive Cell Type and Spatially Specific Clonal Selection in NeurofibromatosisPreprint

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CD81 inhibits the proliferation of astrocytes by inducing G0/G1 arrest in vitro

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