The DOI matches its Crossref record; 61 of the 61 references it cites were found in a registry or an index.
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.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“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]
Citations
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
OPARKA, K. J., Roberts, A. G., Boevink, P. C., Cruz, S. S., Roberts, I. M., Pradel, K. S., Imlau, A., Kotlizky, G., Sauer, N., & Epel, B. L. (1999) · Cell · doi:10.1016/s0092-8674(00)80786-2 · Cited by 465
Functional Connectivity between Immune Cells Mediated by Tunneling Nanotubules
Watkins, S. C., & Salter, R. D. (2005) · Immunity · doi:10.1016/j.immuni.2005.08.009 · Cited by 409
Cutting Edge: Membrane Nanotubes Connect Immune Cells
Önfelt, B., Nedvetzki, S., Yanagi, K., & Davis, D. M. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.3.1511 · Cited by 398
Cell-to-Cell Connection of Endothelial Progenitor Cells With Cardiac Myocytes by Nanotubes
Koyanagi, M., Brandes, R. P., Haendeler, J., Zeiher, A. M., & Dimmeler, S. (2005) · Circulation Research · doi:10.1161/01.res.0000168650.23479.0c · Cited by 331
Motility of ActA protein-coated microspheres driven by actin polymerization
Cameron, L., Footer, M. J., van Oudenaarden, A., & Theriot, J. A. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.9.4908 · Cited by 322
A minimal system allowing tubulation with molecular motors pulling on giant liposomes
Roux, A., Cappello, G., Cartaud, J., Prost, J., Goud, B., & Bassereau, P. M. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.082107299 · Cited by 303
Intercellular Communication in Plants: Studies on Plasmodesmata
Gunning, B. E. S., & Robards, A. W. (1976) · Springer eBooks · doi:10.1007/978-3-642-66294-2 · Cited by 289
Zhu, D., Tan, K. S., Zhang, X., Sun, A. Y., Sun, G. Y., & Lee, J. C.-M. (2005) · Journal of Cell Science · doi:10.1242/jcs.02507 · Cited by 264
Networks of nanotubes and containers
Karlsson, A., Karlsson, R., Karlsson, M., Cans, A.-S. U., Strömberg, A., Ryttsén, F., & Orwar, O. (2001) · Nature · doi:10.1038/35051656 · Cited by 258
The Quest for the Mechanism of Melanin Transfer
Bossche, K. V. D., Naeyaert, J., & Lambert, J. (2006) · Traffic · doi:10.1111/j.1600-0854.2006.00425.x · Cited by 246
Reichelt, S., Knight, A. E., Hodge, T. P., Baluška, F., Šamaj, J., Volkmann, D., & Kendrick‐Jones, J. (1999) · The Plant Journal · doi:10.1046/j.1365-313x.1999.00553.x · Cited by 228
Plasmodesmata: Gatekeepers for Cell-to-Cell Transport of Developmental Signals in Plants
Zambryski, P., & Crawford, K. M. (2000) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.16.1.393 · Cited by 223
Multiple Membrane Tethers Probed by Atomic Force Microscopy
Sun, M., Graham, J. S., Hegedűs, B., Marga, F. S., Zhang, Y., Forgács, G., & Grandbois, M. (2005) · Biophysical Journal · doi:10.1529/biophysj.104.058180 · Cited by 214
Receptor-mediated endocytosis of soluble and membrane-tethered Sonic hedgehog by Patched-1
Incardona, J. P., Lee, J. H., Robertson, C. P., Enga, K., Kapur, R. P., & Roelink, H. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.220251997 · Cited by 199
Ding, B., Kwon, M., & Warnberg, L. (1996) · The Plant Journal · doi:10.1046/j.1365-313x.1996.10010157.x · Cited by 192
Intercellular transfer of P-glycoprotein mediates acquired multidrug resistance in tumor cells
Levchenko, A., Mehta, B. M., Niu, X., Kang, G., Villafania, L. B., Way, D., Polycarpe, D., Sadelain, M., & Larson, S. M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401851102 · Cited by 185
Maize calreticulin localizes preferentially to plasmodesmata in root apex
Baluška, F., Šamaj, J., Napier, R., & Volkmann, D. (1999) · The Plant Journal · doi:10.1046/j.1365-313x.1999.00530.x · Cited by 176
Macromolecular Transport and Signaling Through Plasmodesmata
Heinlein, M., & Epel, B. L. (2004) · International review of cytology · doi:10.1016/s0074-7696(04)35003-5 · Cited by 163
Uptake and Neuritic Transport of Scrapie Prion Protein Coincident with Infection of Neuronal Cells
Magalhães, A. C., Baron, G. S., Lee, K. S., Steele‐Mortimer, O., Dorward, D. W., Prado, M. A. M., & Caughey, B. W. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0653-05.2005 · Cited by 158
Filopodia are conduits for melanosome transfer to keratinocytes
Scott, G., Leopardi, S., Printup, S., & Madden, B. C. (2002) · Journal of Cell Science · doi:10.1242/jcs.115.7.1441 · Cited by 150
Mechanical Measurement of Red Cell Membrane Thickness
Hochmuth, R. M., Evans, C. A., Wiles, H. C., & McCown, J. T. (1983) · Science · doi:10.1126/science.6828875 · Cited by 149
Formation of actin filament bundles in the ring canals of developing Drosophila follicles.
Tilney, L. G., Tilney, M. S., & Guild, G. M. (1996) · The Journal of Cell Biology · doi:10.1083/jcb.133.1.61 · Cited by 116
F-actin rings are associated with the ring canals of the Drosophila egg chamber
Warn, R. M., Gutzeit, H. O., Smith, L., & Warn, A. (1985) · Experimental Cell Research · doi:10.1016/0014-4827(85)90120-x · Cited by 103
Plasmodesmata of maize root tips: structure and composition
Turner, A., Wells, B., & Roberts, K. (1994) · Journal of Cell Science · doi:10.1242/jcs.107.12.3351 · Cited by 100
The plasmodesmatal transport pathway for homeotic proteins, silencing signals and viruses
Ruíz‐Medrano, R., Xoconostle‐Cázares, B., & Kragler, F. (2004) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2004.09.012 · Cited by 99
Localization of a centrin-like protein to higher plant plasmodesmata
Blackman, L. M., Harper, J. D. I., & Overall, R. L. (1999) · European Journal of Cell Biology · doi:10.1016/s0171-9335(99)80063-6 · Cited by 96
Vesicle traffic through intercellular bridges in DU 145 human prostate cancer cells
Vidulescu, C., Clejan, S., & O’Connor, K. C. (2004) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2004.tb00328.x · Cited by 94
Ambudkar, S. V., Sauna, Z. E., Gottesman, M. M., & Szakács, G. (2005) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2005.06.001 · Cited by 91
Not just another hole in the wall: understanding intercellular protein traffickingPreprint
Gallagher, K. L., & Benfey, P. N. (2005) · Genes & Development · doi:10.1101/gad.1271005 · Cited by 91
Plasmodesmata form and function
Heck, M. L., & Jackson, D. P. (2004) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2004.08.002 · Cited by 89
A new interpretation of plasmodesmatal ultrastructure
Robards, A. W. (1968) · Planta · doi:10.1007/bf00398199 · Cited by 89
Guo, G.-Q., & Guo-chang, Z. (2004) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2004.03.010 · Cited by 83
Regulation of short-distance transport of RNA and protein
Kim, J. (2004) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2004.11.005 · Cited by 81
Freund, D., Bauer, N., Boxberger, S., Feldmann, S., Streller, U., Ehninger, G., Werner, C., Bornhäuser, M., Oswald, J., & Corbeil, D. (2006) · Stem Cells and Development · doi:10.1089/scd.2006.15.815 · Cited by 75
Plasma Membrane Sterol Distribution Resembles the Surface Topography of Living Cells
Wüstner, D. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-05-0445 · Cited by 66
Baluška, F., Volkmann, D., & Barlow, P. W. (2007) · Cited by 64
MHC class I alleles and their exploration of the antigen‐processing machinery
Groothuis, T. A., Griekspoor, A., Neijssen, J., Herberts, C. A., & Neefjes, J. (2005) · Immunological Reviews · doi:10.1111/j.0105-2896.2005.00305.x · Cited by 63
Can membrane nanotubes facilitate communication between immune cells?
Önfelt, B., & Davis, D. M. (2004) · Biochemical Society Transactions · doi:10.1042/bst0320676 · Cited by 62
Robards, A. W. (1975) · Annual Review of Plant Physiology · doi:10.1146/annurev.pp.26.060175.000305 · Cited by 58
Getting connected: actin-based cell-to-cell channels in plants and animals
Baluška, F., Hlavačka, A., Volkmann, D., & Menzel, D. (2004) · Trends in Cell Biology · doi:10.1016/j.tcb.2004.07.001 · Cited by 54
Observations on structure and differentiation in plasmodesmata
Burgess, J. (1971) · PROTOPLASMA · doi:10.1007/bf01286414 · Cited by 50
Possible role of phospholipid nanotubes in directed transport of membrane vesicles
Iglič, A., Hägerstrand, H., Bobrowska-Hägerstrand, M., Arrigler, V., & Kralj‐Iglič, V. (2003) · Physics Letters A · doi:10.1016/s0375-9601(03)00449-3 · Cited by 46
Woodruff, R. I., & Tilney, L. G. (1998) · Developmental Biology · doi:10.1006/dbio.1998.8948 · Cited by 33
Analysis of lateral diffusion from a spherical cell surface to a tubular projection
Berk, D. A., Clark, A., & Hochmuth, R. M. (1992) · Biophysical Journal · doi:10.1016/s0006-3495(92)81810-6 · Cited by 29
Automated detection of tunneling nanotubes in 3D images
Hodneland, E., Lundervold, A., Gurke, S., Tai, X., Rustom, A., & Gerdes, H. (2006) · Cytometry Part A · doi:10.1002/cyto.a.20302 · Cited by 26
Self-citationHistorical Perspectives on Plasmodesmata
Carr, D. J. (1976) · Springer eBooks · doi:10.1007/978-3-642-66294-2_14 · Cited by 26
Schmitz, K., & K�hn, R. (1982) · Planta · doi:10.1007/bf01267803 · Cited by 26
Demontis, F. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020215 · Cited by 17
Emerging concept of cancer as a stem cell disorder
Ratajczak, M. Z., Kucia, M., Dobrowolska, H., Wanzeck, J., Reca, R., & Ratajczak, J. (2006) · Open Life Sciences · doi:10.2478/s11535-006-0006-6 · Cited by 12
Endothelial progenitor cells: Neovascularization or more?
Kajstura, J., Leri, A., Bolli, R., & Anversa, P. (2005) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2005.08.007 · Cited by 12
Gerdes, H., & Rustom, A. (2007) · Springer eBooks · doi:10.1007/978-0-387-46957-7_14 · Cited by 7
Self-citation
Flagged first, then by citations
Research works printed but not linked: 1
- 2005 Blackwell Publishing Ltd Oxford K.J. Oparka K.J. Oparka Annual Plant Reviews
Cited by
Sorted by citations
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
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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review