P. D. Arkwright, F. Luchetti, J. Tour, C. Roberts, R. Ayub et al., Fas stimulation of T lymphocytes promotes rapid intercellular exchange of death signals via membrane nanotubes, Cell Research, vol.167, issue.1, pp.72-88, 2010.
DOI : 10.1038/ni1024

J. E. Bear, T. M. Svitkina, M. Krause, D. A. Schafer, J. J. Loureiro et al., Antagonism between Ena/VASP Proteins and Actin Filament Capping Regulates Fibroblast Motility, Cell, vol.109, issue.4, pp.509-521, 2002.
DOI : 10.1016/S0092-8674(02)00731-6

J. S. Berg and R. E. Cheney, Myosin-X is an unconventional myosin that undergoes intrafilopodial motility, Nature Cell Biology, vol.4, issue.3, pp.246-250, 2002.
DOI : 10.1038/ncb762

V. M. Berthoud, P. J. Minogue, J. G. Laing, and E. C. Beyer, Pathways for degradation of connexins and gap junctions, Cardiovascular Research, vol.62, issue.2, pp.256-267, 2004.
DOI : 10.1016/j.cardiores.2003.12.021

B. A. Bour, M. Chakravarti, J. M. West, and S. M. Abmayr, Drosophila SNS, a member of the immunoglobulin superfamily that is essential for myoblast fusion, Genes Dev, vol.14, pp.1498-1511, 2000.

N. V. Bukoreshtliev, X. Wang, E. Hodneland, S. Gurke, J. F. Barroso et al., Selective block of tunneling nanotube (TNT) formation inhibits intercellular organelle transfer between PC12 cells, FEBS Letters, vol.42, issue.9, pp.1481-1488, 2009.
DOI : 10.1016/j.febslet.2009.03.065

R. D. Burgoyne and A. Morgan, Secretory Granule Exocytosis, Physiological Reviews, vol.83, issue.2, pp.581-632, 2003.
DOI : 10.1152/physrev.00031.2002
URL : https://hal.archives-ouvertes.fr/hal-00478869

L. Caneparo, P. Pantazis, W. Dempsey, and S. E. Fraser, Intercellular Bridges in Vertebrate Gastrulation, PLoS ONE, vol.122, issue.5, 2011.
DOI : 10.1371/journal.pone.0020230.s007

E. H. Chen, E. Grote, W. Mohler, and A. Vignery, Cell-cell fusion, FEBS Letters, vol.202, issue.11, pp.2181-2193, 2007.
DOI : 10.1016/j.febslet.2007.03.033

L. V. Chernomordik and M. M. Kozlov, Protein-Lipid Interplay in Fusion and Fission of Biological Membranes, Annual Review of Biochemistry, vol.72, issue.1, pp.175-207, 2003.
DOI : 10.1146/annurev.biochem.72.121801.161504

S. Chifflet, J. A. Hernandez, and S. Grasso, A possible role for membrane depolarization in epithelial wound healing, AJP: Cell Physiology, vol.288, issue.6, pp.1420-1430, 2005.
DOI : 10.1152/ajpcell.00259.2004

H. R. Chinnery, E. Pearlman, and P. G. Mcmenamin, Cells in the Mouse Cornea, The Journal of Immunology, vol.180, issue.9, pp.5779-5783, 2008.
DOI : 10.4049/jimmunol.180.9.5779

M. L. Cilia and D. Jackson, Plasmodesmata form and function, Current Opinion in Cell Biology, vol.16, issue.5, pp.500-506, 2004.
DOI : 10.1016/j.ceb.2004.08.002

D. M. Davis and S. Sowinski, Membrane nanotubes: dynamic long-distance connections between animal cells, Nature Reviews Molecular Cell Biology, vol.23, issue.6, pp.431-436, 2008.
DOI : 10.1038/nrm2399

G. P. Dubey and S. Ben-yehuda, Intercellular Nanotubes Mediate Bacterial Communication, Cell, vol.144, issue.4, pp.590-600, 2011.
DOI : 10.1016/j.cell.2011.01.015
URL : http://doi.org/10.1016/j.cell.2011.01.015

M. L. Dustin, A. K. Chakraborty, and A. S. Shaw, Understanding the Structure and Function of the Immunological Synapse, Cold Spring Harbor Perspectives in Biology, vol.2, issue.10, 2010.
DOI : 10.1101/cshperspect.a002311

H. A. Dworak and H. Sink, Myoblast fusion in Drosophila, BioEssays, vol.110, issue.7, pp.591-601, 2002.
DOI : 10.1002/bies.10115

L. A. Elias, D. D. Wang, and A. R. Kriegstein, Gap junction adhesion is necessary for radial migration in the neocortex, Nature, vol.240, issue.7156, pp.901-907, 2007.
DOI : 10.1038/nature06063

L. A. Elias, M. Turmaine, J. G. Parnavelas, and A. R. Kriegstein, Connexin 43 Mediates the Tangential to Radial Migratory Switch in Ventrally Derived Cortical Interneurons, Journal of Neuroscience, vol.30, issue.20, pp.7072-7077, 2010.
DOI : 10.1523/JNEUROSCI.5728-09.2010

E. A. Eugenin, P. J. Gaskill, and J. W. Berman, Tunneling nanotubes (TNT) are induced by HIV-infection of macrophages: A potential mechanism for intercellular HIV trafficking, Cellular Immunology, vol.254, issue.2, pp.142-148, 2009.
DOI : 10.1016/j.cellimm.2008.08.005

J. Faix and K. Rottner, The making of filopodia, Current Opinion in Cell Biology, vol.18, issue.1, pp.18-25, 2006.
DOI : 10.1016/j.ceb.2005.11.002

H. H. Gerdes and R. N. Carvalho, Intercellular transfer mediated by tunneling nanotubes, Current Opinion in Cell Biology, vol.20, issue.4, pp.470-475, 2008.
DOI : 10.1016/j.ceb.2008.03.005

K. Gousset and C. Zurzolo, Tunnelling nanotubes, Prion, vol.121, issue.2, pp.94-98, 2009.
DOI : 10.1371/journal.ppat.1000426
URL : https://hal.archives-ouvertes.fr/pasteur-00406148

K. Gousset, E. Schiff, C. Langevin, Z. Marijanovic, A. Caputo et al., Prions hijack tunnelling nanotubes for intercellular spread, Nature Cell Biology, vol.177, issue.3, pp.328-336, 2009.
DOI : 10.1038/nprot.2006.356
URL : https://hal.archives-ouvertes.fr/pasteur-00368712

S. Gurke, J. F. Barroso, E. Hodneland, N. V. Bukoreshtliev, O. Schlicker et al., Tunneling nanotube (TNT)-like structures facilitate a constitutive, actomyosin-dependent exchange of endocytic organelles between normal rat kidney cells???, Experimental Cell Research, vol.314, issue.20, pp.3669-3683, 2008.
DOI : 10.1016/j.yexcr.2008.08.022

X. Han, H. Sterling, Y. Chen, C. Saginario, E. J. Brown et al., CD47, a Ligand for the Macrophage Fusion Receptor, Participates in Macrophage Multinucleation, Journal of Biological Chemistry, vol.275, issue.48, pp.37984-37992, 2000.
DOI : 10.1074/jbc.M002334200

K. Hase, S. Ohshima, K. Kawano, N. Hashimoto, K. Matsumoto et al., Distinct Gene Expression Profiles Characterize Cellular Phenotypes of Follicle-Associated Epithelium and M Cells, DNA Research, vol.12, issue.2, pp.127-137, 2005.
DOI : 10.1093/dnares/12.2.127

K. Hase, S. Kimura, H. Takatsu, M. Ohmae, S. Kawano et al., M-Sec promotes membrane nanotube formation by interacting with Ral and the exocyst complex, Nature Cell Biology, vol.281, issue.12, pp.1427-1432, 2009.
DOI : 10.1016/j.cell.2006.08.034

S. C. Hsu, D. Terbush, M. Abraham, and W. Guo, The Exocyst Complex in Polarized Exocytosis, Int. Rev. Cytol, vol.233, pp.243-265, 2004.
DOI : 10.1016/S0074-7696(04)33006-8

M. Ikeda, O. Ishida, T. Hinoi, S. Kishida, and A. Kikuchi, Identification and Characterization of a Novel Protein Interacting with Ral-binding Protein 1, a Putative Effector Protein of Ral, Journal of Biological Chemistry, vol.273, issue.2, pp.814-821, 1998.
DOI : 10.1074/jbc.273.2.814

N. Inoue, M. Ikawa, A. Isotani, and M. Okabe, The immunoglobulin superfamily protein Izumo is required for sperm to fuse with eggs, Nature, vol.54, issue.7030, pp.234-238, 2005.
DOI : 10.1016/S0014-5793(99)00433-0

N. Inoue, M. Ikawa, and M. Okabe, The mechanism of sperm???egg interaction and the involvement of IZUMO1 in fusion, Asian Journal of Andrology, vol.13, issue.1, pp.81-87, 2011.
DOI : 10.1038/aja.2010.70

A. Jegou, A. Ziyyat, V. Barraud-lange, E. Perez, J. P. Wolf et al., CD9 tetraspanin generates fusion competent sites on the egg membrane for mammalian fertilization, Proc. Natl. Acad. Sci. USA, pp.10946-10951, 2011.
DOI : 10.1073/pnas.1017400108

B. P. Jena, Role of SNAREs in Membrane Fusion, Adv. Exp. Med. Biol, vol.713, pp.13-32, 2011.
DOI : 10.1007/978-94-007-0763-4_3

I. Kadiu and H. E. Gendelman, Human Immunodeficiency Virus type 1 Endocytic Trafficking Through Macrophage Bridging Conduits Facilitates Spread of Infection, Journal of Neuroimmune Pharmacology, vol.2, issue.Pt 24, pp.658-675, 2011.
DOI : 10.1007/s11481-011-9298-z

I. Kadiu and H. E. Gendelman, Macrophage Bridging Conduit Trafficking of HIV-1 Through the Endoplasmic Reticulum and Golgi Network, Journal of Proteome Research, vol.10, issue.7, pp.3225-3238, 2011.
DOI : 10.1021/pr200262q

K. Kaji, S. Oda, T. Shikano, T. Ohnuki, Y. Uematsu et al., The gamete fusion process is defective in eggs of Cd9-deficient mice, Nature Genetics, vol.14, issue.3, pp.279-282, 2000.
DOI : 10.1093/molehr/3.12.1087

L. Naour, F. Rubinstein, E. Jasmin, C. Prenant, M. Boucheix et al., Severely Reduced Female Fertility in CD9-Deficient Mice, Science, vol.287, issue.5451, pp.319-321, 2000.
DOI : 10.1126/science.287.5451.319

J. Y. Lee and H. Lu, Plasmodesmata: the battleground against intruders, Trends in Plant Science, vol.16, issue.4, pp.201-210, 2011.
DOI : 10.1016/j.tplants.2011.01.004

W. J. Lucas, B. K. Ham, and J. Y. Kim, Plasmodesmata ??? bridging the gap between neighboring plant cells, Trends in Cell Biology, vol.19, issue.10, pp.495-503, 2009.
DOI : 10.1016/j.tcb.2009.07.003

S. Maeda and T. Tsukihara, Structure of the gap junction channel and its implications for its biological functions, Cellular and Molecular Life Sciences, vol.15, issue.Pt 8, pp.1115-1129, 2011.
DOI : 10.1007/s00018-010-0551-z

S. Martens and H. T. Mcmahon, Mechanisms of membrane fusion: disparate players and common principles, Nature Reviews Molecular Cell Biology, vol.87, issue.7, pp.543-556, 2008.
DOI : 10.1038/nrm2417

T. H. Millard and P. Martin, Dynamic analysis of filopodial interactions during the zippering phase of Drosophila dorsal closure, Development, vol.135, issue.4, pp.621-626, 2008.
DOI : 10.1242/dev.014001

J. Miller, S. E. Fraser, and D. Mcclay, Dynamics of thin filopodia during sea urchin gastrulation, Development, vol.121, pp.2501-2511, 1995.

K. Miyado, G. Yamada, S. Yamada, H. Hasuwa, Y. Nakamura et al., Requirement of CD9 on the Egg Plasma Membrane for Fertilization, Science, vol.287, issue.5451, pp.321-324, 2000.
DOI : 10.1126/science.287.5451.321

K. Miyado, K. Yoshida, K. Yamagata, K. Sakakibara, M. Okabe et al., The fusing ability of sperm is bestowed by CD9-containing vesicles released from eggs in mice, Proc. Natl. Acad. Sci. USA 105, pp.12921-12926, 2008.
DOI : 10.1073/pnas.0710608105

K. Miyazawa, K. Emmerling, and L. Manuelidis, Proliferative arrest of neural cells induces prion protein synthesis, nanotube formation, and cell-to-cell contacts, Journal of Cellular Biochemistry, vol.169, issue.1, pp.239-247, 2010.
DOI : 10.1002/jcb.22723

Y. Ohta, N. Suzuki, S. Nakamura, J. H. Hartwig, and T. P. Stossel, The small GTPase RalA targets filamin to induce filopodia, Proc. Natl. Acad. Sci. USA 96, pp.2122-2128, 1999.
DOI : 10.1073/pnas.96.5.2122

B. Onfelt, S. Nedvetzki, K. Yanagi, and D. M. Davis, Cutting Edge: Membrane Nanotubes Connect Immune Cells, The Journal of Immunology, vol.173, issue.3, pp.1511-1513, 2004.
DOI : 10.4049/jimmunol.173.3.1511

B. Onfelt, S. Nedvetzki, R. K. Benninger, M. A. Purbhoo, S. Sowinski et al., Structurally Distinct Membrane Nanotubes between Human Macrophages Support Long-Distance Vesicular Traffic or Surfing of Bacteria, The Journal of Immunology, vol.177, issue.12, pp.8476-8483, 2006.
DOI : 10.4049/jimmunol.177.12.8476

C. Pyrgaki, P. Trainor, A. K. Hadjantonakis, and L. Niswander, Dynamic imaging of mammalian neural tube closure, Developmental Biology, vol.344, issue.2, pp.941-947, 2010.
DOI : 10.1016/j.ydbio.2010.06.010

P. Rakic, Developmental and Evolutionary Adaptations of Cortical Radial Glia, Cerebral Cortex, vol.13, issue.6, pp.541-549, 2003.
DOI : 10.1093/cercor/13.6.541

F. A. Ramirez-weber and T. B. Kornberg, Cytonemes, Cell, vol.97, issue.5, pp.599-607, 1999.
DOI : 10.1016/S0092-8674(00)80771-0

A. J. Ridley, Life at the Leading Edge, Cell, vol.145, issue.7, pp.1012-1022, 2011.
DOI : 10.1016/j.cell.2011.06.010

S. Roy, F. Hsiung, and T. B. Kornberg, Specificity of Drosophila Cytonemes for Distinct Signaling Pathways, Science, vol.332, issue.6027, pp.354-358, 2011.
DOI : 10.1126/science.1198949

R. Rozental, M. Srinivas, S. Gokhan, M. Urban, R. Dermietzel et al., Temporal expression of neuronal connexins during hippocampal ontogeny, Brain Research Reviews, vol.32, issue.1, pp.57-71, 2000.
DOI : 10.1016/S0165-0173(99)00096-X

E. Rubinstein, A. Ziyyat, J. P. Wolf, L. Naour, F. Boucheix et al., The molecular players of sperm???egg fusion in mammals, Seminars in Cell & Developmental Biology, vol.17, issue.2, pp.254-263, 2006.
DOI : 10.1016/j.semcdb.2006.02.012

M. Ruiz-gomez, N. Coutts, A. Price, M. V. Taylor, and M. Bate, Drosophila Dumbfounded, Cell, vol.102, issue.2, pp.189-198, 2000.
DOI : 10.1016/S0092-8674(00)00024-6

I. Rupp, L. Sologub, K. C. Williamson, M. Scheuermayer, L. Reininger et al., Malaria parasites form filamentous cell-to-cell connections during reproduction in the mosquito midgut, Cell Research, vol.28, issue.4, pp.683-696, 2011.
DOI : 10.1017/S0031182000013202

A. Rustom, R. Saffrich, I. Markovic, P. Walther, and H. H. Gerdes, Nanotubular Highways for Intercellular Organelle Transport, Science, vol.303, issue.5660, pp.1007-1010, 2004.
DOI : 10.1126/science.1093133

C. Saginario, H. Sterling, C. Beckers, R. Kobayashi, M. Solimena et al., MFR, a Putative Receptor Mediating the Fusion of Macrophages, Molecular and Cellular Biology, vol.18, issue.11, pp.6213-6223, 1998.
DOI : 10.1128/MCB.18.11.6213

E. Salas-vidal and H. Lomeli, Imaging filopodia dynamics in the mouse blastocyst, Developmental Biology, vol.265, issue.1, pp.75-89, 2004.
DOI : 10.1016/j.ydbio.2003.09.012

V. Sarma, F. W. Wolf, R. M. Marks, T. B. Shows, and V. M. Dixit, Cloning of a novel tumor necrosis factor-alpha-inducible primary response gene that is differentially expressed in development and capillary tube-like formation in vitro, J. Immunol, vol.148, pp.3302-3312, 1992.

D. A. Schafer, Cell biology: Barbed ends rule, Nature, vol.118, issue.7001, pp.734-735, 2004.
DOI : 10.1016/S0092-8674(02)00731-6

N. M. Sherer and W. Mothes, Cytonemes and tunneling nanotubules in cell???cell communication and viral pathogenesis, Trends in Cell Biology, vol.18, issue.9, pp.414-420, 2008.
DOI : 10.1016/j.tcb.2008.07.003

S. K. Singh, R. Kurfurst, C. Nizard, S. Schnebert, E. Perrier et al., Melanin transfer in human skin cells is mediated by filopodia--a model for homotypic and heterotypic lysosome-related organelle transfer, The FASEB Journal, vol.24, issue.10, pp.3756-3769, 2010.
DOI : 10.1096/fj.10-159046

I. F. Smith, J. Shuai, and I. Parker, Active Generation and Propagation of Ca2+ Signals within Tunneling Membrane Nanotubes, Biophysical Journal, vol.100, issue.8, pp.37-39, 2011.
DOI : 10.1016/j.bpj.2011.03.007

S. Sowinski, C. Jolly, O. Berninghausen, M. A. Purbhoo, A. Chauveau et al., Membrane nanotubes physically connect T cells over long distances presenting a novel route for HIV-1 transmission, Nature Cell Biology, vol.8, issue.2, pp.211-219, 2008.
DOI : 10.1074/jbc.C400046200

M. Strunkelnberg, B. Bonengel, L. M. Moda, A. Hertenstein, H. G. De-couet et al., rst and its paralogue kirre act redundantly during embryonic muscle development in Drosophila, Development, vol.128, pp.4229-4239, 2001.

T. Tabata and Y. Takei, Morphogens, their identification and regulation, Development, vol.131, issue.4, pp.703-712, 2004.
DOI : 10.1242/dev.01043
URL : http://dev.biologists.org/cgi/content/short/131/4/703

J. M. Teddy and P. M. Kulesa, In vivo evidence for short- and long-range cell communication in cranial neural crest cells, Development, vol.131, issue.24, pp.6141-6151, 2004.
DOI : 10.1242/dev.01534

E. M. Van-dam and P. J. Robinson, Ral: Mediator of membrane trafficking, The International Journal of Biochemistry & Cell Biology, vol.38, issue.11, pp.1841-1847, 2006.
DOI : 10.1016/j.biocel.2006.04.006

A. Vignery, Osteoclasts and giant cells: macrophage-macrophage fusion mechanism, International Journal of Experimental Pathology, vol.95, issue.40, pp.291-304, 2000.
DOI : 10.1111/j.1365-2613.2000.00164.x
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2517739

X. Wang and H. H. Gerdes, Long-distance electrical coupling via tunneling nanotubes, Biochimica et Biophysica Acta (BBA) - Biomembranes, vol.1818, issue.8, 2011.
DOI : 10.1016/j.bbamem.2011.09.002
URL : http://doi.org/10.1016/j.bbamem.2011.09.002

X. Wang, M. L. Veruki, N. V. Bukoreshtliev, E. Hartveit, and H. H. Gerdes, Animal cells connected by nanotubes can be electrically coupled through interposed gap-junction channels, Proc. Natl. Acad. Sci. USA, pp.17194-17199, 2010.
DOI : 10.1073/pnas.1006785107

Y. Wang, J. Cui, X. Sun, and Y. Zhang, Tunneling-nanotube development in astrocytes depends on p53 activation, Cell Death and Differentiation, vol.23, issue.4, pp.732-742, 2011.
DOI : 10.1038/cdd.2010.147

S. C. Watkins and R. D. Salter, Functional Connectivity between Immune Cells Mediated by Tunneling Nanotubules, Immunity, vol.23, issue.3, pp.309-318, 2005.
DOI : 10.1016/j.immuni.2005.08.009
URL : http://doi.org/10.1016/j.immuni.2005.08.009

C. J. Wei, R. Francis, X. Xu, and C. W. Lo, Connexin43 Associated with an N-cadherin-containing Multiprotein Complex Is Required for Gap Junction Formation in NIH3T3 Cells, Journal of Biological Chemistry, vol.280, issue.20, 2005.
DOI : 10.1074/jbc.M412921200

W. Wood, A. Jacinto, R. Grose, S. Woolner, J. Gale et al., Wound healing recapitulates morphogenesis in Drosophila embryos, Nature Cell Biology, vol.27, issue.11, pp.907-912, 2002.
DOI : 10.1007/s004270050246

W. Xu, P. A. Santini, J. S. Sullivan, B. He, M. Shan et al., HIV-1 evades virus-specific IgG2 and IgA responses by targeting systemic and intestinal B cells via long-range intercellular conduits, Nature Immunology, vol.393, issue.9, pp.1008-1017, 2009.
DOI : 10.1038/ni.1753

K. Yasuda, A. Khandare, L. Burianovskyy, S. Maruyama, F. Zhang et al., Tunneling nanotubes mediate rescue of prematurely senescent endothelial cells by endothelial progenitors: exchange of lysosomal pool, Aging, vol.3, issue.6, pp.597-608, 2011.
DOI : 10.18632/aging.100341

M. Zhao, B. Song, J. Pu, T. Wada, B. Reid et al., Electrical signals control wound healing through phosphatidylinositol-3-OH kinase-?? and PTEN, Nature, vol.109, issue.7101, pp.457-460, 2006.
DOI : 10.1038/nature04925