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Tunneling nanotubes: A new route for the exchange of components between animal cells
Abstract
Recently, highly sensitive nanotubular structures mediating membrane continuity between mammalian cells have been discovered. With respect to their peculiar architecture, these membrane channels were termed tunneling nanotubes (TNTs). TNTs could form de novo between animal cells leading to the generation of complex cellular networks. They have been shown to facilitate the intercellular transfer of organelles as well as, on a limited scale, of membrane components and cytoplasmic molecules. It has been proposed that TNTs represent a novel and general biological principle of cell‐to‐cell communication and it becomes increasingly apparent that they fulfill important functions in the physiological processes of multicellular organisms.
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“Later, HIV-1 and HTLV-1 cell-to-cell transmission via TNT was reported.”
From HIV-1 and HTLV-1 Transmission Modes: Mechanisms and Importance for Virus Spread (2022) · cites this paper as [107]
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Cites
Südhof, T. C. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.26.041002.131412 · Cited by 2,491
Nanotubular Highways for Intercellular Organelle Transport
Rustom, A., Saffrich, R., Markovic, I., Walther, P., & Gerdes, H.-H. (2004) · Science · doi:10.1126/science.1093133 · Cited by 2,038
Self-citationThe Gap Junction Communication Channel
Kumar, N. M., & Gilula, N. B. (1996) · Cell · doi:10.1016/s0092-8674(00)81282-9 · Cited by 1,929
Cholesterol Modification of Hedgehog Signaling Proteins in Animal Development
Porter, J. A., Young, K. E., & Beachy, P. A. (1996) · Science · doi:10.1126/science.274.5285.255 · Cited by 1,360
The Biogenesis and Functions of Exosomes
Stoorvogel, W., Kleijmeer, M. J., Geuze, H. J., & Raposo, G. (2002) · Traffic · doi:10.1034/j.1600-0854.2002.30502.x · Cited by 848
Identification of a Palmitic Acid-modified Form of Human Sonic hedgehog
Pepinsky, R. B., Zeng, C., Wen, D., Rayhorn, P., Baker, D. P., Williams, K. P., Bixler, S. A., Ambrose, C. M., Garber, E. A., Miatkowski, K., et al. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.22.14037 · Cited by 754
Ramı́rez-Weber, F.-A., & Kornberg, T. B. (1999) · Cell · doi:10.1016/s0092-8674(00)80771-0 · Cited by 614
The origin of the cancer stem cell: current controversies and new insights
Bjerkvig, R., Tysnes, B. B., Aboody, K. S., Najbauer, J., & Terzis, A. J. A. (2005) · Nature reviews. Cancer · doi:10.1038/nrc1740 · Cited by 604
STUDIES ON THE FINE STRUCTURE OF THE MAMMALIAN TESTIS
Burgos, M. H., & Fawcett, D. W. (1955) · The Journal of Cell Biology · doi:10.1083/jcb.1.4.287 · Cited by 561
Önfelt, B., Nedvetzki, S., Benninger, R. K. P., Purbhoo, M. A., Sowinski, S., Hume, A. N., Seabra, M. C., Neil, M. A. A., French, P. M. W., & Davis, D. M. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.177.12.8476 · Cited by 503
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Sowinski, S., Jolly, C., Berninghausen, O., Purbhoo, M. A., Chauveau, A., Köhler, K., Oddos, S., Eissmann, P., Brodsky, F. M., Hopkins, C., et al. (2008) · Nature Cell Biology · doi:10.1038/ncb1682 · Cited by 754
Astrocytes and Glioblastoma cells release exosomes carrying mtDNA
Guescini, M., Genedani, S., Stocchi, V., & Agnati, L. F. (2009) · Journal of Neural Transmission · doi:10.1007/s00702-009-0288-8 · Cited by 662
Prions hijack tunnelling nanotubes for intercellular spread
Gousset, K., Schiff, E., Langevin, C., Marijanovic, Z., Caputo, A., Browman, D., Chenouard, N., de Chaumont, F., Martino, A., Enninga, J., et al. (2009) · Nature Cell Biology · doi:10.1038/ncb1841 · Cited by 639
Avoiding the void: Cell-to-cell spread of human viruses
Sattentau, Q. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1972 · Cited by 614
Pasquier, J., Guerrouahen, B. S., Al-Thawadi, H., Ghiabi, P., Maleki, M., Abu-Kaoud, N., Jacob, A., Mirshahi, M., Galas, L., Rafii, S., et al. (2013) · Journal of Translational Medicine · doi:10.1186/1479-5876-11-94 · Cited by 514
Mitochondria Know No Boundaries: Mechanisms and Functions of Intercellular Mitochondrial Transfer
Torralba, D., Baixauli, F., & Sánchez-Madrid, F. (2016) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2016.00107 · Cited by 440
Tunneling-nanotube development in astrocytes depends on p53 activation
Wang, Y., Cui, J., Sun, X., & Zhang, Y. (2010) · Cell Death and Differentiation · doi:10.1038/cdd.2010.147 · Cited by 422
M-Sec promotes membrane nanotube formation by interacting with Ral and the exocyst complex
Hase, K., Kimura, S., Takatsu, H., Ohmae, M., Kawano, S., Kitamura, H., Ito, M., Watarai, H., Hazelett, C. C., Yeaman, C., et al. (2009) · Nature Cell Biology · doi:10.1038/ncb1990 · Cited by 402
Membrane nanotubes: dynamic long-distance connections between animal cells
Davis, D. M., & Sowinski, S. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2399 · Cited by 377
Mitochondrial function in hypoxic ischemic injury and influence of aging
Ham, P. B., & Raju, R. P. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.06.006 · Cited by 374
Regenerative abilities of mesenchymal stem cells through mitochondrial transfer
Paliwal, S., Chaudhuri, R., Agrawal, A., & Mohanty, S. (2018) · Journal of Biomedical Science · doi:10.1186/s12929-018-0429-1 · Cited by 343
Intercellular transfer mediated by tunneling nanotubes
Gerdes, H., & Carvalho, R. (2008) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2008.03.005 · Cited by 324
Self-citationTunneling nanotube (TNT)-mediated neuron-to neuron transfer of pathological Tau protein assemblies
Tardivel, M., Bégard, S., Bousset, L., Dujardin, S., Coens, A., Melki, R., Buée, L., & Colin, M. (2016) · Acta Neuropathologica Communications · doi:10.1186/s40478-016-0386-4 · Cited by 305
Eugenin, E. A., Gaskill, P. J., & Berman, J. W. (2009) · Cellular Immunology · doi:10.1016/j.cellimm.2008.08.005 · Cited by 304
C2C12 myoblasts release micro-vesicles containing mtDNA and proteins involved in signal transduction
Guescini, M., Guidolin, D., Vallorani, L., Casadei, L., Gioacchini, A. M., Tibollo, P., Battistelli, M., Falcieri, E., Battistin, L., Agnati, L. F., et al. (2010) · Experimental Cell Research · doi:10.1016/j.yexcr.2010.04.006 · Cited by 294
The discovery of central monoamine neurons gave volume transmission to the wired brain
Fuxé, K., Dahlström, A. B., JONSSON, G., Marcellino, D. J., Guescini, M., Dam, M., Manger, P. R., & Agnati, L. F. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.10.012 · Cited by 285
Cutting Edge: Membrane Nanotubes In Vivo: A Feature of MHC Class II+ Cells in the Mouse Cornea
Chinnery, H. R., Pearlman, E. M., & McMenamin, P. G. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.9.5779 · Cited by 278
Ariazi, J. L., Benowitz, A. B., de Biasi, V., den Boer, M. L., Cherqui, S., Cui, H., Douillet, N., Eugenín, E. A., Favre, D., Goodman, S. M., et al. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00333 · Cited by 250
Exosomal transfer of proteins and RNAs at synapses in the nervous system
Smalheiser, N. R. (2007) · Biology Direct · doi:10.1186/1745-6150-2-35 · Cited by 256
Cell‐to‐cell cross‐talk between mesenchymal stem cells and cardiomyocytes in co‐culture
Plotnikov, E. Y., Khryapenkova, T. G., Vasileva, A. K., Marey, M. V., Galkina, S. I., Исаев, Н. К., Sheval, E. V., Polyakov, V. Y., Sukhikh, G. T., & Zorov, D. B. (2008) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2007.00205.x · Cited by 244
Exosomes as a Nanodelivery System: a Key to the Future of Neuromedicine?
Aryani, A., & Denecke, B. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-9054-5 · Cited by 242
Bukoreshtliev, N. V., Wang, X., Hodneland, E., Gurke, S., Barroso, J., & Gerdes, H. (2009) · FEBS Letters · doi:10.1016/j.febslet.2009.03.065 · Cited by 226
Self-citationExtracellular Vesicles: Evolving Factors in Stem Cell Biology
Nawaz, M., Fatima, F., Vallabhaneni, K. C., Penfornis, P., Valadi, H., Ekström, K. M., Kholia, S., Whitt, J. D., Fernandes, J. D., Pochampally, R. R., et al. (2015) · Stem Cells International · doi:10.1155/2016/1073140 · Cited by 227
Chowdhury, D. (2013) · Physics Reports · doi:10.1016/j.physrep.2013.03.005 · Cited by 221
The art of cellular communication: tunneling nanotubes bridge the divide
Gurke, S., Barroso, J. F., & Gerdes, H. (2008) · Histochemistry and Cell Biology · doi:10.1007/s00418-008-0412-0 · Cited by 210
Self-citationBustamante-Barrientos, F. A., Luque‐Campos, N., Araya, M. J., Lara-Barba, E., Solminihac, J. D., Pradenas, C., Molina, L., Herrera-Luna, Y., Utreras‐Mendoza, Y., Elizondo-Vega, R. J., et al. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04493-w · Cited by 204
Lu, J., Zheng, X., Li, F., Yu, Y., Chen, Z., Liu, Z., Wang, Z., Xu, H., & Yang, W. (2017) · Oncotarget · doi:10.18632/oncotarget.14695 · Cited by 185
Plotnikov, E. Y., Khryapenkova, T. G., Galkina, S. I., Sukhikh, G. T., & Zorov, D. B. (2010) · Experimental Cell Research · doi:10.1016/j.yexcr.2010.06.009 · Cited by 180
Peering into tunneling nanotubes—The path forward
Cervantes, D. C., & Zurzolo, C. (2021) · The EMBO Journal · doi:10.15252/embj.2020105789 · Cited by 175
Jia, L., Zhou, Z., Liang, H., Wu, J., Shi, P., Li, F., Wang, Z., Wang, C., Chen, W., Zhang, H., et al. (2015) · Oncogene · doi:10.1038/onc.2015.263 · Cited by 178
Human T-cell leukemia virus type 1 p8 protein increases cellular conduits and virus transmission
Van Prooyen, N., Gold, H., Andresen, V., Schwartz, O., Jones, K., Ruscetti, F., Lockett, S., Gudla, P., Venzon, D., & Franchini, G. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009635107 · Cited by 178
Role of Human Mesenchymal Stem Cells in Regenerative Therapy
Vasanthan, J., Gurusamy, N., Rajasingh, S., Sigamani, V., Kirankumar, S., Thomas, E. L., & Rajasingh, J. (2020) · Cells · doi:10.3390/cells10010054 · Cited by 186
Mitochondrial Transfer and Regulators of Mesenchymal Stromal Cell Function and Therapeutic Efficacy
Mohammadalipour, A., Dumbali, S. P., & Wenzel, P. L. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.603292 · Cited by 182
Multifaceted Roles of Tunneling Nanotubes in Intercellular Communication
Marzo, L., Gousset, K., & Zurzolo, C. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00072 · Cited by 177
Inter and Intracellular mitochondrial trafficking in health and disease
Shanmughapriya, S., Langford, D., & Natarajaseenivasan, K. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101128 · Cited by 171
Mechanisms of cellular communication through intercellular protein transfer
Ahmed, K. A., & Xiang, J. (2010) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2010.01008.x · Cited by 153
Artificial Mitochondria Transfer: Current Challenges, Advances, and Future Applications
Caicedo, A., Aponte, P. M., Cabrera, F., Hidalgo, C., & Khoury, M. (2017) · Stem Cells International · doi:10.1155/2017/7610414 · Cited by 150
Gurke, S., Barroso, J. F., Hodneland, E., Bukoreshtliev, N. V., Schlicker, O., & Gerdes, H. (2008) · Experimental Cell Research · doi:10.1016/j.yexcr.2008.08.022 · Cited by 148
Self-citationTunneling Nanotubes and Tumor Microtubes in Cancer
Roehlecke, C., & Schmidt, M. H. H. (2020) · Cancers · doi:10.3390/cancers12040857 · Cited by 147
Forms of extracellular mitochondria and their impact in health
Miliotis, S., Nicolalde, B., Ortega, M., Yepez, J., & Caicedo, A. (2019) · Mitochondrion · doi:10.1016/j.mito.2019.02.002 · Cited by 138
New Insights into the Cell Biology of Hematopoietic Progenitors by Studying Prominin-1 (CD133)
Bauer, N., Fonseca, A., Florek, M., Freund, D., Jászai, J., Bornhäuser, M., Fargeas, C. A., & Corbeil, D. (2007) · Cells Tissues Organs · doi:10.1159/000112847 · Cited by 137
Different Types of Cell-to-Cell Connections Mediated by Nanotubular Structures
Veranič, P., Lokar, M., Schütz, G. J., Weghuber, J., Wieser, S., Hägerstrand, H., Kralj‐Iglič, V., & Iglič, A. (2008) · Biophysical Journal · doi:10.1529/biophysj.108.131375 · Cited by 135
Murray, L. M. A., & Krasnodembskaya, A. D. (2018) · Stem Cells · doi:10.1002/stem.2922 · Cited by 140
Dilsizoglu Senol, A., Samarani, M., Syan, S., Guardia, C. M., Nonaka, T., Liv, N., Latour-Lambert, P., Hasegawa, M., Klumperman, J., Bonifacino, J. S., et al. (2021) · PLOS Biology · doi:10.1371/journal.pbio.3001287 · Cited by 134
Robicsek, O., Ene, H. M., Karry, R., Ytzhaki, O., Asor, E., McPhie, D. L., Cohen, B. M., Ben-Yehuda, R., Weiner, I., & Ben‐Shachar, D. (2017) · Schizophrenia Bulletin · doi:10.1093/schbul/sbx077 · Cited by 135
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Nawaz, M., & Fatima, F. (2017) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2017.00050 · Cited by 120
Sharma, S., LeClaire, M. D., & Gimzewski, J. K. (2018) · Nanotechnology · doi:10.1088/1361-6528/aaab06 · Cited by 122
Multi-Level Communication of Human Retinal Pigment Epithelial Cells via Tunneling Nanotubes
Wittig, D., Wang, X., Walter, C., Gerdes, H., Funk, R. H. W., & Roehlecke, C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0033195 · Cited by 118
Self-citationThe Functions, Methods, and Mobility of Mitochondrial Transfer Between Cells
Qin, Y., Jiang, X., Yang, Q., Zhao, J., Zhou, Q., & Zhou, Y. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.672781 · Cited by 120
Domhan, S., Ma, L.-L., Tai, A., Anaya, Z., Beheshti, A., Zeier, M., Hlatky, L., & Abdollahi, A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021283 · Cited by 109
Paliwal, S., Chaudhuri, R., Agrawal, A., & Mohanty, S. (2018) · Stem Cell Research & Therapy · doi:10.1186/s13287-018-1012-0 · Cited by 117
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Dong, L., Rohlena, J., Zobalová, R., Nahácka, Z., Rodriguez, A., Berridge, M. V., & Neužil, J. (2023) · The Journal of Cell Biology · doi:10.1083/jcb.202211044 · Cited by 118
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Vingtdeux, V., Sergeant, N., & Buée, L. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00229 · Cited by 116
Emerging physiological and pathological implications of tunneling nanotubes formation between cells
Sisakhtnezhad, S., & Khosravi, L. (2015) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2015.06.010 · Cited by 118
Cell-to-cell communication in plants, animals, and fungi: a comparative review
Bloemendal, S., & Kück, U. (2012) · Die Naturwissenschaften · doi:10.1007/s00114-012-0988-z · Cited by 108
Mechanisms and functions for the duration of intercellular contacts made by lymphocytes
Davis, D. M. (2009) · Nature reviews. Immunology · doi:10.1038/nri2602 · Cited by 106
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Dunning, C. J. R., Reyes, J. F., Steiner, J. A., & Brundin, P. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.11.003 · Cited by 111
Bacterial survival strategies suggest rethinking cancer cooperativity
Ben‐Jacob, E., Coffey, D. S., & Levine, H. (2012) · Trends in Microbiology · doi:10.1016/j.tim.2012.06.001 · Cited by 105
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Valenti, D., Vacca, R. A., Moro, L., & Atlante, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158312 · Cited by 100
Kadiu, I., & Gendelman, H. E. (2011) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-011-9298-z · Cited by 100
Mesenchymal stem cell-mediated transfer of mitochondria: mechanisms and functional impact
Velarde, F., Ezquerra, S., Delbruyere, X., Caicedo, A., Hidalgo, Y., & Khoury, M. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04207-3 · Cited by 109
Low-Level Laser Effect on Proliferation, Migration, and Antiapoptosis of Mesenchymal Stem Cells
Yin, K., Zhu, R., Wang, S., & Zhao, R. C. (2017) · Stem Cells and Development · doi:10.1089/scd.2016.0332 · Cited by 92
Stress-induced tunneling nanotubes support treatment adaptation in prostate cancer
Kretschmer, A., Zhang, F., Somasekharan, S. P., Tse, C., Leachman, L., Gleave, A., Li, B., Asmaro, I., Huang, T., Kotula, L., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-44346-5 · Cited by 92
Gousset, K., & Zurzolo, C. (2009) · Prion · doi:10.4161/pri.3.2.8917 · Cited by 92
Porcine Reproductive and Respiratory Syndrome Virus Utilizes Nanotubes for Intercellular Spread
Guo, R., Katz, B. B., Tomich, J. M., Gallagher, T., & Fāng, Y. (2016) · Journal of Virology · doi:10.1128/jvi.00036-16 · Cited by 90
Matrix as an Interstitial Transport System
Dong, F., Creemers, E. E., & Kassiri, Z. (2014) · Circulation Research · doi:10.1161/circresaha.114.302335 · Cited by 91
Tunneling nanotubes evoke pericyte/endothelial communication during normal and tumoral angiogenesis
Errede, M., Mangieri, D., Longo, G., Girolamo, F., de Trizio, I., Vimercati, A., Serio, G., Frei, K., Perris, R., & Virgintino, D. (2018) · Fluids and Barriers of the CNS · doi:10.1186/s12987-018-0114-5 · Cited by 88
Macrophage Bridging Conduit Trafficking of HIV-1 Through the Endoplasmic Reticulum and Golgi Network
Kadiu, I., & Gendelman, H. E. (2011) · Journal of Proteome Research · doi:10.1021/pr200262q · Cited by 85
Role of Tunneling Nanotubes in Viral Infection, Neurodegenerative Disease, and Cancer
Tiwari, V., Koganti, R., Russell, G., Sharma, A., & Shukla, D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.680891 · Cited by 86
Rhes travels from cell to cell and transports Huntington disease protein via TNT-like protrusion
Sharma, M., & Subramaniam, S. (2019) · Journal of Cell Biology · doi:10.1083/jcb.201807068 · Cited by 76
Zhang, L., & Zhang, Y. (2015) · Neuroscience Bulletin · doi:10.1007/s12264-014-1522-4 · Cited by 83
Agnati, L. F., & Fuxé, K. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0505 · Cited by 79
Tunneling nanotubes and related structures: molecular mechanisms of formation and function
Dagar, S., Pathak, D., Oza, H. V., & Mylavarapu, S. V. S. (2021) · Biochemical Journal · doi:10.1042/bcj20210077 · Cited by 79
Controlling the rates of biochemical reactions and signaling networks by shape and volume changes
Lizana, L., BAUER, B. E., & Orwar, O. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709932105 · Cited by 76
The cytoskeleton in plasmodesmata: a role in intercellular transport?
White, R. G., & Barton, D. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err227 · Cited by 76
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He, K., Luo, W., Zhang, Y., Liu, F., Liu, D., Xu, L., Qin, L., Xiong, C., Lu, Z., Fang, X., et al. (2010) · ACS Nano · doi:10.1021/nn1002198 · Cited by 79
Impenetrable barriers or entry portals? The role of cell–cell adhesion during infection
Bonazzi, M., & Cossart, P. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201106011 · Cited by 77
Civita, P., Leite, D. M., & Pilkington, G. J. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20236017 · Cited by 74
Valdebenito, S., Audia, A., Bhat, K., Okafo, G., & Eugenin, E. (2020) · iScience · doi:10.1016/j.isci.2020.101450 · Cited by 58
Nair, S., Rocha‐Ferreira, E., Fleiss, B., Nijboer, C. H. A., Gressèns, P., Mallard, C. E., & Hagberg, H. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.15267 · Cited by 73
Osteikoetxea-Molnár, A., Szabó‐Meleg, E., Tóth, E. A., Oszvald, Á., Izsépi, E., Kremlitzka, M., Biri‐Kovács, B., Nyitray, L., Bozó, T., Németh, P., et al. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2233-y · Cited by 69
New perspectives of tissue remodelling with neural stem and progenitor cell-based therapies
Cossetti, C., Alfaro‐Cervelló, C., Donegà, M., Tyzack, G. E., & Pluchino, S. (2012) · Cell and Tissue Research · doi:10.1007/s00441-012-1341-8 · Cited by 69
Novel mechanisms of central nervous system damage in HIV infection
Eugenin, E. (2010) · HIV/AIDS - Research and Palliative Care · doi:10.2147/hiv.s9186 · Cited by 70
Eugenín, E. A., Gaskill, P. J., & Berman, J. W. (2009) · Communicative & Integrative Biology · doi:10.4161/cib.2.3.8165 · Cited by 72
HIV-1 and HTLV-1 Transmission Modes: Mechanisms and Importance for Virus Spread
Kalinichenko, S., Komkov, D., & Mazurov, D. (2022) · Viruses · doi:10.3390/v14010152 · Cited by 68
“TNTs are formed between cells of the immune system, neurons, and glial cells, and provide intercellular communication over long distances to transport calcium, genetic material, proteins, and organelles [107].”
BackgroundSeyed‐Razavi, Y., Hickey, M. J., Kuffová, L., McMenamin, P. G., & Chinnery, H. R. (2012) · Immunology and Cell Biology · doi:10.1038/icb.2012.52 · Cited by 70
Understanding Fibroblasts in Order to Comprehend the Osteopathic Treatment of the Fascia
Bordoni, B., & Zanier, E. (2015) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2015/860934 · Cited by 67
Nanofilaments on glioblastoma exosomes revealed by peak force microscopy
Sharma, S., Das, K., Woo, J., & Gimzewski, J. K. (2014) · Journal of The Royal Society Interface · doi:10.1098/rsif.2013.1150 · Cited by 65
Reichert, D., Scheinpflug, J., Karbanová, J., Freund, D., Bornhäuser, M., & Corbeil, D. (2016) · Experimental Hematology · doi:10.1016/j.exphem.2016.07.006 · Cited by 64
New insights into cytomixis: specific cellular features and prevalence in higher plants
Mursalimov, S. R., Sidorchuk, Y. V., & Дейнеко, Е. В. (2013) · Planta · doi:10.1007/s00425-013-1914-0 · Cited by 63
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Metadata
- Authors
- Gerdes, H.-H., Bukoreshtliev, N. V., & Barroso, J. F. V.
- Affiliations
- University of Bergen (NO)
- Corresponding author
- Gerdes, Hans-Hermann
- Venue
- FEBS Letters
- Publisher
- Wiley
- Published
- 2007-04-04
- Volume
- 581
- Issue
- 11
- Pages
- 2194-2201
- ISSN
- 0014-5793 (ISSN-L)
- 1873-3468
- OpenAlex
- W2044320361
- Cited by
- 304
- References
- 61
- Citations by year
- 2026: 9 · 2025: 6 · 2024: 18 · 2023: 11 · 2022: 18 · 2021: 20 · 2020: 18 · 2019: 18 · 2018: 21 · 2017: 16 · 2016: 14 · 2015: 13 · 2014: 11 · 2013: 14 · 2012: 22
- FWCI
- 1.34
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- FEBS Letters (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Caveolin-1 and cellular processes
- Keywords
- tunneling nanotubes, intercellular communication, membrane continuity, organelle transfer, multicellular organisms
- MeSH terms
- Animals, Biological Transport, Cell Communication, Cell Membrane, Humans, Plasmodesmata, Nanotubes
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