Alberts, P., Rudge, R., Hinners, I., Muzerelle, A., Martinez-Arca, S., Irinopoulou, T., Marthiens, V., Tooze, S., Rathjen, F., Gaspar, P., Galli, T., Cross talk between tetanus neurotoxin-insensitive vesicle-associated membrane protein-mediated transport and L1-mediated adhesion. Mol. Biol. Cell 14 (2003), 4207–4220.
Aoyagi, K., Itakura, M., Fukutomi, T., Nishiwaki, C., Nakamichi, Y., Torii, S., Makiyama, T., Harada, A., Ohara-Imaizumi, M., VAMP7 Regulates Autophagosome Formation by Supporting Atg9a Functions in Pancreatic β-Cells From Male Mice. Endocrinology 159 (2018), 3674–3688.
Bai, L., Mei, X., Shen, Z., Bi, Y., Yuan, Y., Guo, Z., Wang, H., Zhao, H., Zhou, Z., Wang, C., et al. Netrin-1 Improves Functional Recovery through Autophagy Regulation by Activating the AMPK/mTOR Signaling Pathway in Rats with Spinal Cord Injury. Sci. Rep., 7, 2017, 42288.
Birgisdottir, Å.B., Lamark, T., Johansen, T., The LIR motif - crucial for selective autophagy. J. Cell Sci. 126 (2013), 3237–3247.
Bobrie, A., Colombo, M., Krumeich, S., Raposo, G., Théry, C., Diverse subpopulations of vesicles secreted by different intracellular mechanisms are present in exosome preparations obtained by differential ultracentrifugation. J. Extracell. Vesicles, 1, 2012 10.3402/jev.v1i0.18397.
Boya, P., Reggiori, F., Codogno, P., Emerging regulation and functions of autophagy. Nat. Cell Biol. 15 (2013), 713–720.
Bradke, F., Dotti, C.G., Differentiated neurons retain the capacity to generate axons from dendrites. Curr. Biol. 10 (2000), 1467–1470.
Burgo, A., Proux-Gillardeaux, V., Sotirakis, E., Bun, P., Casano, A., Verraes, A., Liem, R.K.H., Formstecher, E., Coppey-Moisan, M., Galli, T., A molecular network for the transport of the TI-VAMP/VAMP7 vesicles from cell center to periphery. Dev. Cell 23 (2012), 166–180.
Burgo, A., Casano, A.M., Kuster, A., Arold, S.T., Wang, G., Nola, S., Verraes, A., Dingli, F., Loew, D., Galli, T., Increased activity of the vesicular soluble N-ethylmaleimide-sensitive factor attachment protein receptor TI-VAMP/VAMP7 by tyrosine phosphorylation in the Longin domain. J. Biol. Chem. 288 (2013), 11960–11972.
Cáceres, A., Ye, B., Dotti, C.G., Neuronal polarity: demarcation, growth and commitment. Curr. Opin. Cell Biol. 24 (2012), 547–553.
Chari, R., Yeo, N.C., Chavez, A., Church, G.M., sgRNA Scorer 2.0: A Species-Independent Model To Predict CRISPR/Cas9 Activity. ACS Synth. Biol. 6 (2017), 902–904.
Chávez-López, S., de Jesús Lugo-Trampe, J., Ibarra-Ramírez, M., Calvo-Anguiano, G., Martínez-de-Villarreal, L.E., Campos-Acevedo, L.D., A case series of infants with increased vamp7 gene dosage at birth and virilization defects. J. Pediatr. Urol. 16 (2020), 423.e1–423.e6.
Coco, S., Raposo, G., Martinez, S., Fontaine, J.J., Takamori, S., Zahraoui, A., Jahn, R., Matteoli, M., Louvard, D., Galli, T., Subcellular localization of tetanus neurotoxin-insensitive vesicle-associated membrane protein (VAMP)/VAMP7 in neuronal cells: evidence for a novel membrane compartment. J. Neurosci. 19 (1999), 9803–9812.
Colombo, F., Racchetti, G., Meldolesi, J., Neurite outgrowth induced by NGF or L1CAM via activation of the TrkA receptor is sustained also by the exocytosis of enlargeosomes. Proc. Natl. Acad. Sci. USA 111 (2014), 16943–16948.
Cotrufo, T., Pérez-Brangulí, F., Muhaisen, A., Ros, O., Andrés, R., Baeriswyl, T., Fuschini, G., Tarrago, T., Pascual, M., Ureña, J., et al. A signaling mechanism coupling netrin-1/deleted in colorectal cancer chemoattraction to SNARE-mediated exocytosis in axonal growth cones. J. Neurosci. 31 (2011), 14463–14480.
Cox, J., Mann, M., MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification. Nat. Biotechnol. 26 (2008), 1367–1372.
Cunningham, C.N., Williams, J.M., Knupp, J., Arunagiri, A., Arvan, P., Tsai, B., Cells Deploy a Two-Pronged Strategy to Rectify Misfolded Proinsulin Aggregates. Mol. Cell 75 (2019), 442–456.e4.
Danglot, L., Zylbersztejn, K., Petkovic, M., Gauberti, M., Meziane, H., Combe, R., Champy, M.-F., Birling, M.-C., Pavlovic, G., Bizot, J.-C., et al. Absence of TI-VAMP/Vamp7 leads to increased anxiety in mice. J. Neurosci. 32 (2012), 1962–1968.
de Chaumont, F., Dallongeville, S., Chenouard, N., Hervé, N., Pop, S., Provoost, T., Meas-Yedid, V., Pankajakshan, P., Lecomte, T., Le Montagner, Y., et al. Icy: an open bioimage informatics platform for extended reproducible research. Nat. Methods 9 (2012), 690–696.
Di Scala, F., Dupuis, L., Gaiddon, C., De Tapia, M., Jokic, N., Gonzalez de Aguilar, J.-L., Raul, J.-S., Ludes, B., Loeffler, J.-P., Tissue specificity and regulation of the N-terminal diversity of reticulon 3. Biochem. J. 385 (2005), 125–134.
Dotti, C.G., Sullivan, C.A., Banker, G.A., The establishment of polarity by hippocampal neurons in culture. J. Neurosci. 8 (1988), 1454–1468.
EauClaire, S., Guo, W., Conservation and specialization. The role of the exocyst in neuronal exocytosis. Neuron 37 (2003), 369–370.
Ellert-Miklaszewska, A., Ciechomska, I.A., Kaminska, B., Cannabinoid signaling in glioma cells. Adv. Exp. Med. Biol. 1202 (2020), 223–241.
Fader, C.M., Aguilera, M.O., Colombo, M.I., ATP is released from autophagic vesicles to the extracellular space in a VAMP7-dependent manner. Autophagy 8 (2012), 1741–1756.
Fuschini, G., Cotrufo, T., Ros, O., Muhaisen, A., Andrés, R., Comella, J.X., Soriano, E., Syntaxin-1/TI-VAMP SNAREs interact with Trk receptors and are required for neurotrophin-dependent outgrowth. Oncotarget 9 (2018), 35922–35940.
Ghosh, D., Pinto, S., Danglot, L., Vandewauw, I., Segal, A., Van Ranst, N., Benoit, M., Janssens, A., Vennekens, R., Vanden Berghe, P., et al. VAMP7 regulates constitutive membrane incorporation of the cold-activated channel TRPM8. Nat. Commun., 7, 2016, 10489.
Grassi, D., Plonka, F.B., Oksdath, M., Guil, A.N., Sosa, L.J., Quiroga, S., Selected SNARE proteins are essential for the polarized membrane insertion of igf-1 receptor and the regulation of initial axonal outgrowth in neurons. Cell Discov., 1, 2015, 15023.
Greene, L.A., Tischler, A.S., Establishment of a noradrenergic clonal line of rat adrenal pheochromocytoma cells which respond to nerve growth factor. Proc. Natl. Acad. Sci. USA 73 (1976), 2424–2428.
Grumati, P., Morozzi, G., Hölper, S., Mari, M., Harwardt, M.I., Yan, R., Müller, S., Reggiori, F., Heilemann, M., Dikic, I., Full length RTN3 regulates turnover of tubular endoplasmic reticulum via selective autophagy. eLife, 6, 2017, e25555.
Gupton, S.L., Gertler, F.B., Integrin signaling switches the cytoskeletal and exocytic machinery that drives neuritogenesis. Dev. Cell 18 (2010), 725–736.
Havé, M., Luo, J., Tellier, F., Balliau, T., Cueff, G., Chardon, F., Zivy, M., Rajjou, L., Cacas, J.-L., Masclaux-Daubresse, C., Proteomic and lipidomic analyses of the Arabidopsis atg5 autophagy mutant reveal major changes in endoplasmic reticulum and peroxisome metabolisms and in lipid composition. New Phytol. 223 (2019), 1461–1477.
Hesketh, G.G., Pérez-Dorado, I., Jackson, L.P., Wartosch, L., Schäfer, I.B., Gray, S.R., McCoy, A.J., Zeldin, O.B., Garman, E.F., Harbour, M.E., et al. VARP is recruited on to endosomes by direct interaction with retromer, where together they function in export to the cell surface. Dev. Cell 29 (2014), 591–606.
Hu, X., Shi, Q., Zhou, X., He, W., Yi, H., Yin, X., Gearing, M., Levey, A., Yan, R., Transgenic mice overexpressing reticulon 3 develop neuritic abnormalities. EMBO J. 26 (2007), 2755–2767.
Ikemoto, A., Okuyama, H., Differential utilization of the ethanolamine moiety of phosphatidylethanolamine derived from serine and ethanolamine during NGF-induced neuritogenesis of PC12 cells. Neurochem. Res. 25 (2000), 293–301.
Itakura, E., Kishi-Itakura, C., Mizushima, N., The hairpin-type tail-anchored SNARE syntaxin 17 targets to autophagosomes for fusion with endosomes/lysosomes. Cell 151 (2012), 1256–1269.
Jausoro, I., Marzolo, M.-P., Reelin activates the small GTPase TC10 and VAMP7 to promote neurite outgrowth and regeneration of dorsal root ganglia (DRG) neurons. J. Neurosci. Res. 99 (2021), 392–406.
Jewell, J.L., Guan, K.-L., Nutrient signaling to mTOR and cell growth. Trends Biochem. Sci. 38 (2013), 233–242.
Jiang, W., Ogretmen, B., Autophagy paradox and ceramide. Biochim. Biophys. Acta 1841 (2014), 783–792.
Kabeya, Y., Mizushima, N., Yamamoto, A., Oshitani-Okamoto, S., Ohsumi, Y., Yoshimori, T., LC3, GABARAP and GATE16 localize to autophagosomal membrane depending on form-II formation. J. Cell Sci. 117 (2004), 2805–2812.
Kaushik, S., Massey, A.C., Mizushima, N., Cuervo, A.M., Constitutive activation of chaperone-mediated autophagy in cells with impaired macroautophagy. Mol. Biol. Cell 19 (2008), 2179–2192.
Kim, J., Kundu, M., Viollet, B., Guan, K.-L., AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1. Nat. Cell Biol. 13 (2011), 132–141.
Kirchner, P., Bourdenx, M., Madrigal-Matute, J., Tiano, S., Diaz, A., Bartholdy, B.A., Will, B., Cuervo, A.M., Proteome-wide analysis of chaperone-mediated autophagy targeting motifs. PLoS Biol., 17, 2019, e3000301.
Kowal, J., Tkach, M., Théry, C., Biogenesis and secretion of exosomes. Curr. Opin. Cell Biol. 29 (2014), 116–125.
Kuster, A., Nola, S., Dingli, F., Vacca, B., Gauchy, C., Beaujouan, J.-C., Nunez, M., Moncion, T., Loew, D., Formstecher, E., et al. The Q-soluble N-Ethylmaleimide-sensitive Factor Attachment Protein Receptor (Q-SNARE) SNAP-47 Regulates Trafficking of Selected Vesicle-associated Membrane Proteins (VAMPs). J. Biol. Chem. 290 (2015), 28056–28069.
Lagache, T., Sauvonnet, N., Danglot, L., Olivo-Marin, J.-C., Statistical analysis of molecule colocalization in bioimaging. Cytometry A 87 (2015), 568–579.
Leidal, A.M., Huang, H.H., Marsh, T., Solvik, T., Zhang, D., Ye, J., Kai, F., Goldsmith, J., Liu, J.Y., Huang, Y.-H., et al. The LC3-conjugation machinery specifies the loading of RNA-binding proteins into extracellular vesicles. Nat. Cell Biol. 22 (2020), 187–199.
Liu, J., Xia, H., Kim, M., Xu, L., Li, Y., Zhang, L., Cai, Y., Norberg, H.V., Zhang, T., Furuya, T., et al. Beclin1 controls the levels of p53 by regulating the deubiquitination activity of USP10 and USP13. Cell 147 (2011), 223–234.
Loi, M., Raimondi, A., Morone, D., Molinari, M., ESCRT-III-driven piecemeal micro-ER-phagy remodels the ER during recovery from ER stress. Nat. Commun., 10, 2019, 5058.
Longair, M.H., Baker, D.A., Armstrong, J.D., Simple Neurite Tracer: open source software for reconstruction, visualization and analysis of neuronal processes. Bioinformatics 27 (2011), 2453–2454.
Martinez-Arca, S., Alberts, P., Zahraoui, A., Louvard, D., Galli, T., Role of tetanus neurotoxin insensitive vesicle-associated membrane protein (TI-VAMP) in vesicular transport mediating neurite outgrowth. J. Cell Biol. 149 (2000), 889–900.
Martinez-Arca, S., Coco, S., Mainguy, G., Schenk, U., Alberts, P., Bouillé, P., Mezzina, M., Prochiantz, A., Matteoli, M., Louvard, D., Galli, T., A common exocytotic mechanism mediates axonal and dendritic outgrowth. J. Neurosci. 21 (2001), 3830–3838.
Matsushita, M., Suzuki, N.N., Obara, K., Fujioka, Y., Ohsumi, Y., Inagaki, F., Structure of Atg5.Atg16, a complex essential for autophagy. J. Biol. Chem. 282 (2007), 6763–6772.
Matz, J., Chames, P., Phage display and selections on purified antigens. Methods Mol. Biol. 907 (2012), 213–224.
Mauvezin, C., Neufeld, T.P., Bafilomycin A1 disrupts autophagic flux by inhibiting both V-ATPase-dependent acidification and Ca-P60A/SERCA-dependent autophagosome-lysosome fusion. Autophagy 11 (2015), 1437–1438.
McLelland, G.-L., Lee, S.A., McBride, H.M., Fon, E.A., Syntaxin-17 delivers PINK1/parkin-dependent mitochondrial vesicles to the endolysosomal system. J. Cell Biol. 214 (2016), 275–291.
Mizushima, N., Yoshimori, T., Ohsumi, Y., The role of Atg proteins in autophagosome formation. Annu. Rev. Cell Dev. Biol. 27 (2011), 107–132.
Mordier, S., Deval, C., Béchet, D., Tassa, A., Ferrara, M., Leucine limitation induces autophagy and activation of lysosome-dependent proteolysis in C2C12 myotubes through a mammalian target of rapamycin-independent signaling pathway. J. Biol. Chem. 275 (2000), 29900–29906.
Moreau, K., Ravikumar, B., Renna, M., Puri, C., Rubinsztein, D.C., Autophagosome precursor maturation requires homotypic fusion. Cell 146 (2011), 303–317.
Moutel, S., Bery, N., Bernard, V., Keller, L., Lemesre, E., de Marco, A., Ligat, L., Rain, J.-C., Favre, G., Olichon, A., et al. NaLi-H1: A universal synthetic library of humanized nanobodies providing highly functional antibodies and intrabodies. Elife, 5, 2016.
Mutoh, T., Tokuda, A., Inokuchi, J., Kuriyama, M., Glucosylceramide synthase inhibitor inhibits the action of nerve growth factor in PC12 cells. J. Biol. Chem. 273 (1998), 26001–26007.
Ogura, K., Goshima, Y., The autophagy-related kinase UNC-51 and its binding partner UNC-14 regulate the subcellular localization of the Netrin receptor UNC-5 in Caenorhabditis elegans. Development 133 (2006), 3441–3450.
Olivo-Marin, J.-C., Extraction of spots in biological images using multiscale products. Pattern Recognit 35 (2002), 1989–1996.
Ollion, J., Cochennec, J., Loll, F., Escudé, C., Boudier, T., TANGO: a generic tool for high-throughput 3D image analysis for studying nuclear organization. Bioinformatics 29 (2013), 1840–1841.
Omari, S., Makareeva, E., Roberts-Pilgrim, A., Mirigian, L., Jarnik, M., Ott, C., Lippincott-Schwartz, J., Leikin, S., Noncanonical autophagy at ER exit sites regulates procollagen turnover. Proc. Natl. Acad. Sci. USA 115 (2018), E10099–E10108.
Petkovic, M., Jemaiel, A., Daste, F., Specht, C.G., Izeddin, I., Vorkel, D., Verbavatz, J.-M., Darzacq, X., Triller, A., Pfenninger, K.H., et al. The SNARE Sec22b has a non-fusogenic function in plasma membrane expansion. Nat. Cell Biol. 16 (2014), 434–444.
Proux-Gillardeaux, V., Raposo, G., Irinopoulou, T., Galli, T., Expression of the Longin domain of TI-VAMP impairs lysosomal secretion and epithelial cell migration. Biol. Cell 99 (2007), 261–271.
Racchetti, G., Lorusso, A., Schulte, C., Gavello, D., Carabelli, V., D'Alessandro, R., Meldolesi, J., Rapid neurite outgrowth in neurosecretory cells and neurons is sustained by the exocytosis of a cytoplasmic organelle, the enlargeosome. J. Cell Sci. 123 (2010), 165–170.
Ramírez-Peinado, S., León-Annicchiarico, C.L., Galindo-Moreno, J., Iurlaro, R., Caro-Maldonado, A., Prehn, J.H.M., Ryan, K.M., Muñoz-Pinedo, C., Glucose-starved cells do not engage in prosurvival autophagy. J. Biol. Chem. 288 (2013), 30387–30398.
Rockenfeller, P., Koska, M., Pietrocola, F., Minois, N., Knittelfelder, O., Sica, V., Franz, J., Carmona-Gutierrez, D., Kroemer, G., Madeo, F., Phosphatidylethanolamine positively regulates autophagy and longevity. Cell Death Differ. 22 (2015), 499–508.
Romanov, J., Walczak, M., Ibiricu, I., Schüchner, S., Ogris, E., Kraft, C., Martens, S., Mechanism and functions of membrane binding by the Atg5-Atg12/Atg16 complex during autophagosome formation. EMBO J. 31 (2012), 4304–4317.
Roy, S., Leidal, A.M., Ye, J., Ronen, S.M., Debnath, J., Autophagy-Dependent Shuttling of TBC1D5 Controls Plasma Membrane Translocation of GLUT1 and Glucose Uptake. Mol. Cell 67 (2017), 84–95.e5.
Ruhl, D.A., Bomba-Warczak, E., Watson, E.T., Bradberry, M.M., Peterson, T.A., Basu, T., Frelka, A., Evans, C.S., Briguglio, J.S., Basta, T., et al. Synaptotagmin 17 controls neurite outgrowth and synaptic physiology via distinct cellular pathways. Nat. Commun., 10, 2019, 3532.
Sahu, R., Kaushik, S., Clement, C.C., Cannizzo, E.S., Scharf, B., Follenzi, A., Potolicchio, I., Nieves, E., Cuervo, A.M., Santambrogio, L., Microautophagy of cytosolic proteins by late endosomes. Dev. Cell 20 (2011), 131–139.
Savaraj, N., You, M., Wu, C., Wangpaichitr, M., Kuo, M.T., Feun, L.G., Arginine deprivation, autophagy, apoptosis (AAA) for the treatment of melanoma. Curr. Mol. Med. 10 (2010), 405–412.
Schindelin, J., Arganda-Carreras, I., Frise, E., Kaynig, V., Longair, M., Pietzsch, T., Preibisch, S., Rueden, C., Saalfeld, S., Schmid, B., et al. Fiji: an open-source platform for biological-image analysis. Nat. Methods 9 (2012), 676–682.
Schneider, C.A., Rasband, W.S., Eliceiri, K.W., NIH Image to ImageJ: 25 years of image analysis. Nat. Methods 9 (2012), 671–675.
Sekine, Y., Lindborg, J.A., Strittmatter, S.M., A proteolytic C-terminal fragment of Nogo-A (reticulon-4A) is released in exosomes and potently inhibits axon regeneration. J. Biol. Chem. 295 (2020), 2175–2183.
Sharoar, M.G., Shi, Q., Ge, Y., He, W., Hu, X., Perry, G., Zhu, X., Yan, R., Dysfunctional tubular endoplasmic reticulum constitutes a pathological feature of Alzheimer's disease. Mol. Psychiatry 21 (2016), 1263–1271.
Siddiqi, S.A., Siddiqi, S., Mahan, J., Peggs, K., Gorelick, F.S., Mansbach, C.M. 2nd, The identification of a novel endoplasmic reticulum to Golgi SNARE complex used by the prechylomicron transport vesicle. J. Biol. Chem. 281 (2006), 20974–20982.
Takáts, S., Nagy, P., Varga, Á., Pircs, K., Kárpáti, M., Varga, K., Kovács, A.L., Hegedűs, K., Juhász, G., Autophagosomal Syntaxin17-dependent lysosomal degradation maintains neuronal function in Drosophila. J. Cell Biol. 201 (2013), 531–539.
Song, J.-W., Lam, S.M., Fan, X., Cao, W.-J., Wang, S.-Y., Tian, H., Chua, G.H., Zhang, C., Meng, F.-P., Xu, Z., et al. Omics-Driven Systems Interrogation of Metabolic Dysregulation in COVID-19 Pathogenesis. Cell Metab 32 (2020), 188–202.e5.
Takáts, S., Glatz, G., Szenci, G., Boda, A., Horváth, G.V., Hegedűs, K., Kovács, A.L., Juhász, G., Non-canonical role of the SNARE protein Ykt6 in autophagosome-lysosome fusion. PLoS Genet., 14, 2018, e1007359.
Takei, N., Nawa, H., mTOR signaling and its roles in normal and abnormal brain development. Front. Mol. Neurosci., 7, 2014, 28.
Tamura, H., Shibata, M., Koike, M., Sasaki, M., Uchiyama, Y., Atg9A protein, an autophagy-related membrane protein, is localized in the neurons of mouse brains. J. Histochem. Cytochem. 58 (2010), 443–453.
Tannour-Louet, M., Han, S., Louet, J.-F., Zhang, B., Romero, K., Addai, J., Sahin, A., Cheung, S.W., Lamb, D.J., Increased gene copy number of VAMP7 disrupts human male urogenital development through altered estrogen action. Nat. Med. 20 (2014), 715–724.
Thukral, L., Sengupta, D., Ramkumar, A., Murthy, D., Agrawal, N., Gokhale, R.S., The Molecular Mechanism Underlying Recruitment and Insertion of Lipid-Anchored LC3 Protein into Membranes. Biophys. J. 109 (2015), 2067–2078.
Vega, I.E., Hsu, S.C., The exocyst complex associates with microtubules to mediate vesicle targeting and neurite outgrowth. J. Neurosci. 21 (2001), 3839–3848.
Verderio, C., Cagnoli, C., Bergami, M., Francolini, M., Schenk, U., Colombo, A., Riganti, L., Frassoni, C., Zuccaro, E., Danglot, L., et al. TI-VAMP/VAMP7 is the SNARE of secretory lysosomes contributing to ATP secretion from astrocytes. Biol. Cell 104 (2012), 213–228.
Verraes, A., Cholley, B., Galli, T., Nola, S., Comparative study of commercially available and homemade anti-VAMP7 antibodies using CRISPR/Cas9-depleted HeLa cells and VAMP7 knockout mice. F1000Res., 7, 2018, 1649.
Viswanath, P., Radoul, M., Izquierdo-Garcia, J.L., Ong, W.Q., Luchman, H.A., Cairncross, J.G., Huang, B., Pieper, R.O., Phillips, J.J., Ronen, S.M., 2-Hydroxyglutarate-Mediated Autophagy of the Endoplasmic Reticulum Leads to an Unusual Downregulation of Phospholipid Biosynthesis in Mutant IDH1 Gliomas. Cancer Res. 78 (2018), 2290–2304.
Voeltz, G.K., Prinz, W.A., Shibata, Y., Rist, J.M., Rapoport, T.A., A class of membrane proteins shaping the tubular endoplasmic reticulum. Cell 124 (2006), 573–586.
Wakana, Y., Koyama, S., Nakajima, K., Hatsuzawa, K., Nagahama, M., Tani, K., Hauri, H.-P., Melançon, P., Tagaya, M., Reticulon 3 is involved in membrane trafficking between the endoplasmic reticulum and Golgi. Biochem. Biophys. Res. Commun. 334 (2005), 1198–1205.
West, M., Zurek, N., Hoenger, A., Voeltz, G.K., A 3D analysis of yeast ER structure reveals how ER domains are organized by membrane curvature. J. Cell Biol. 193 (2011), 333–346.
Winkle, C.C., McClain, L.M., Valtschanoff, J.G., Park, C.S., Maglione, C., Gupton, S.L., A novel Netrin-1-sensitive mechanism promotes local SNARE-mediated exocytosis during axon branching. J. Cell Biol. 205 (2014), 217–232.
Witte, H., Neukirchen, D., Bradke, F., Microtubule stabilization specifies initial neuronal polarization. J. Cell Biol. 180 (2008), 619–632.