Developmental control of cell morphogenesis: a focus on membrane growth (original) (raw)
Gumbiner, B.M. Cell adhesion: the molecular basis of tissue architecture and morphogenesis. Cell84, 345–357 (1996). CASPubMed Google Scholar
Mitchison, T.J. & Cramer, L.P. Actin-based cell motility and cell locomotion. Cell84, 371–379 (1996). CASPubMed Google Scholar
Bretscher, M.S. Distribution of receptors for transferrin and low density lipoprotein on the surface of giant HeLa cells. Proc. Natl Acad. Sci. USA80, 454–458 (1983). CASPubMedPubMed Central Google Scholar
Bretscher, M.S. Moving membrane up to the front of migrating cells. Cell85, 465–467 (1996). CASPubMed Google Scholar
Bretscher, M.S. & Aguado-Velasco, C. Membrane traffic during cell locomotion. Curr. Opin. Cell Biol.10, 537–541 (1998). CASPubMed Google Scholar
Drubin, D.G. & Nelson, W.J. Origins of cell polarity. Cell84, 335–44 (1996). CASPubMed Google Scholar
Neiman, A.M. Prospore membrane formation defines a developmentally regulated branch of the secretory pathway in yeast. J. Cell Biol.140, 29–37 (1998). CASPubMedPubMed Central Google Scholar
Fullilove, S.L. & Jacobson, A.G. Nuclear elongation and cytokinesis in Drosophila montana. Dev. Biol.26, 560–577 (1971). CASPubMed Google Scholar
Foe, V.E., Odell, G.M. and Edgar, B.A. Mitosis and morphogenesis in the Drosophila embryo: point and counterpoint. in The Development of Drosophila melanogaster, Vol. 1 149–300 (Cold Spring Harbor Laboratory Press, 1993). Google Scholar
Loncar, D. & Singer, S.J. Cell membrane formation during the cellularization of the syncytial blastoderm of Drosophila. Proc. Natl Acad. Sci. USA92, 2199–2203 (1995). CASPubMedPubMed Central Google Scholar
Lecuit, T. & Wieschaus, E. Polarized insertion of new membrane from a cytoplasmic reservoir during cleavage of the Drosophila embryo. J. Cell Biol.150, 849–860 (2000). CASPubMedPubMed Central Google Scholar
Zecevic, N. & Rakic, P. Differentiation of Purkinje cells and their relationship to other components of developing cerebellar cortex in man. J. Comp. Neurol.167, 27–47 (1976). CASPubMed Google Scholar
Bradke, F. & Dotti, C.G. Establishment of neuronal polarity: lessons from cultured hippocampal neurons. Curr. Opin. Neurobiol.10, 574–581 (2000). CASPubMed Google Scholar
Wolff, T. & Ready, D.F. in The Development of Drosophila melanogaster (eds Martinez-Arias, A. & Bate, M.) (Cold Spring Harbor Press, Cold Spring Harbor, 1993). Google Scholar
Izaddoost, S., Nam, S.C., Bhat, M.A., Bellen, H.J. & Choi, K.W. Drosophila Crumbs is a positional cue in photoreceptor adherens junctions and rhabdomeres. Nature416, 178–183 (2002). CASPubMed Google Scholar
Pellikka, M. et al. Crumbs, the Drosophila homologue of human CRB1/RP12, is essential for photoreceptor morphogenesis. Nature416, 143–149 (2002). CASPubMed Google Scholar
Sisson, J.C., Field, C., Ventura, R., Royou, A. & Sullivan, W. Lava Lamp, a novel peripheral Golgi protein, is required for Drosophila melanogaster cellularization. J. Cell Biol.151, 905–918 (2000). CASPubMedPubMed Central Google Scholar
Wirtz, H.R. & Dobbs, L.G. Calcium mobilization and exocytosis after one mechanical stretch of lung epithelial cells. Science250, 1266–1269 (1990). CASPubMed Google Scholar
Truschel, S.T. et al. Stretch-regulated exocytosis/endocytosis in bladder umbrella cells. Mol. Biol. Cell13, 830–846 (2002). CASPubMedPubMed Central Google Scholar
Echard, A. et al. Interaction of a Golgi-associated kinesin-like protein with Rab6. Science279, 580–585 (1998). CASPubMed Google Scholar
Hill, E., Clarke, M. & Barr, F.A. The Rab6-binding kinesin, Rab6-KIFL, is required for cytokinesis. EMBO J.19, 5711–5719 (2000). CASPubMedPubMed Central Google Scholar
Satoh, A., Tokunaga, F., Kawamura, S. & Ozaki, K. In situ inhibition of vesicle transport and protein processing in the dominant negative Rab1 mutant of Drosophila. J. Cell Sci.110, 2943–2953 (1997). CASPubMed Google Scholar
Gagnon, E. et al. Endoplasmic reticulum-mediated phagocytosis is a mechanism of entry into macrophages. Cell110, 119–131 (2002). CASPubMed Google Scholar
Franco, M. et al. EFA6, a sec7 domain-containing exchange factor for ARF6, coordinates membrane recycling and actin cytoskeleton organization. EMBO J.18, 1480–1491 (1999). CASPubMedPubMed Central Google Scholar
Bajno, L. et al. Focal exocytosis of VAMP3-containing vesicles at sites of phagosome formation. J. Cell Biol.149, 697–706 (2000). CASPubMedPubMed Central Google Scholar
Derrien, V. et al. A conserved C-terminal domain of EFA6-family ARF6-guanine nucleotide exchange factors induces lengthening of microvilli-like membrane protrusions. J. Cell Sci.115, 2867–2879 (2002). CASPubMed Google Scholar
Aguado-Velasco, C. & Bretscher, M.S. Circulation of the plasma membrane in Dictyostelium. Mol. Biol. Cell10, 4419–4427 (1999). CASPubMedPubMed Central Google Scholar
Hopkins, C.R., Gibson, A., Shipman, M., Strickland, D.K. & Trowbridge, I.S. In migrating fibroblasts, recycling receptors are concentrated in narrow tubules in the pericentriolar area, and then routed to the plasma membrane of the leading lamella. J. Cell Biol.125, 1265–1274 (1994). CASPubMed Google Scholar
Laukaitis, C.M., Webb, D.J., Donais, K. & Horwitz, A.F. Differential dynamics of α5 integrin, paxillin, and α-actinin during formation and disassembly of adhesions in migrating cells. J. Cell Biol.153, 1427–1440 (2001). CASPubMedPubMed Central Google Scholar
Lawson, M.A. & Maxfield, F.R. Calcium- and calcineurin-dependent recycling of an integrin to the front of migrating neutrophils. Nature377, 75–79 (1995). CASPubMed Google Scholar
Kamiguchi, H. & Lemmon, V. Recycling of the cell adhesion molecule L1 in axonal growth cones. J. Neurosci.20, 3676–3686 (2000). CASPubMedPubMed Central Google Scholar
Kamiguchi, H. et al. The neural cell adhesion molecule L1 interacts with the AP-2 adaptor and is endocytosed via the clathrin-mediated pathway. J. Neurosci.18, 5311–5321 (1998). CASPubMedPubMed Central Google Scholar
Kamiguchi, H. & Yoshihara, F. The role of endocytic l1 trafficking in polarized adhesion and migration of nerve growth cones. J. Neurosci.21, 9194–9203 (2001). CASPubMedPubMed Central Google Scholar
Fournier, A.E. et al. Semaphorin3A enhances endocytosis at sites of receptor–F-actin colocalization during growth cone collapse. J. Cell Biol.149, 411–22 (2000). CASPubMedPubMed Central Google Scholar
Radhakrishna, H. & Donaldson, J.G. ADP-ribosylation factor 6 regulates a novel plasma membrane recycling pathway. J. Cell Biol.139, 49–61 (1997). CASPubMedPubMed Central Google Scholar
Peters, P.J. et al. Overexpression of wild-type and mutant ARF1 and ARF6: distinct perturbations of nonoverlapping membrane compartments. J. Cell Biol.128, 1003–1017 (1995). CASPubMed Google Scholar
D'Souza-Schorey, C., Li, G., Colombo, M.I. & Stahl, P.D. A regulatory role for ARF6 in receptor-mediated endocytosis. Science267, 1175–1178 (1995). CASPubMed Google Scholar
D'Souza-Schorey, C. et al. ARF6 targets recycling vesicles to the plasma membrane: insights from an ultrastructural investigation. J. Cell Biol.140, 603–616 (1998). CASPubMedPubMed Central Google Scholar
Radhakrishna, H., Al-Awar, O., Khachikian, Z. & Donaldson, J.G. ARF6 requirement for Rac ruffling suggests a role for membrane trafficking in cortical actin rearrangements. J. Cell Sci.112, 855–66 (1999). CASPubMed Google Scholar
Burgess, R.W., Deitcher, D.L. & Schwarz, T.L. The synaptic protein syntaxin1 is required for cellularization of Drosophila embryos. J. Cell Biol.138, 861–875 (1997). CASPubMedPubMed Central Google Scholar
Jantsch-Plunger, V. & Glotzer, M. Depletion of syntaxins in the early Caenorhabditis elegans embryo reveals a role for membrane fusion events in cytokinesis. Curr. Biol.9, 738–745 (1999). CASPubMed Google Scholar
Lauber, M.H. et al. The Arabidopsis knolle protein is a cytokinesis-specific syntaxin. J. Cell Biol.139, 1485–1493 (1997). CASPubMedPubMed Central Google Scholar
Waizenegger, I. et al. The Arabidopsis knolle and keule genes interact to promote vesicle fusion during cytokinesis. Curr. Biol.10, 1371–1374 (2000). CASPubMed Google Scholar
McNiven, M.A. Dynamin: a molecular motor with pinchase action. Cell94, 151–154 (1998). CASPubMed Google Scholar
Swanson, M.P., CA. The _shibire_-ts mutant of Drosophila: a probe for the study of embryonic development. Dev. Biol.84, 465–470 (1981). CASPubMed Google Scholar
Skop, A.R., Bergmann, D., Mohler, W.A. & White, J.G. Completion of cytokinesis in C. elegans requires a brefeldin A-sensitive membrane accumulation at the cleavage furrow apex. Curr. Biol.11, 735–746 (2001). CASPubMedPubMed Central Google Scholar
Ullrich, O., Reinsch, S., Urbe, S., Zerial, M. & Parton, R.G. Rab11 regulates recycling through the pericentriolar recycling endosome. J. Cell Biol.135, 913–924 (1996). CASPubMed Google Scholar
Schweitzer, J.K. & D'Souza-Schorey, C. Localization and activation of the ARF6 GTPase during cleavage furrow ingression and cytokinesis. J. Biol. Chem.277, 27210–27216 (2002). CASPubMed Google Scholar
Bodmer, R. & Venkatesh, T.V. Heart development in Drosophila and vertebrates: conservation of molecular mechanisms. Dev. Genet.22, 181–186 (1998). CASPubMed Google Scholar
Chartier, A., Zaffran, S., Astier, M., Semeriva, M. & Gratecos, D. Pericardin, a Drosophila type IV collagen-like protein is involved in the morphogenesis and maintenance of the heart epithelium during dorsal ectoderm closure. Development129, 3241–3253 (2002). CASPubMed Google Scholar
Ponzielli, R. et al. Heart tube patterning in Drosophila requires integration of axial and segmental information provided by the Bithorax Complex genes and hedgehog signaling. Development129, 4509–4521 (2002). CASPubMed Google Scholar
Lee, T., Hacohen, N., Krasnow, M. & Montell, D.J. Regulated Breathless receptor tyrosine kinase activity required to pattern cell migration and branching in the Drosophila tracheal system. Genes Dev.10, 2912–2921 (1996). CASPubMed Google Scholar
Sutherland, D., Samakovlis, C. & Krasnow, M.A. branchless encodes a Drosophila FGF homolog that controls tracheal cell migration and the pattern of branching. Cell87, 1091–101 (1996). CASPubMed Google Scholar
Metzger, R.J. & Krasnow, M.A. Genetic control of branching morphogenesis. Science284, 1635–1639 (1999). CASPubMed Google Scholar
Ribeiro, C., Ebner, A. & Affolter, M. In vivo imaging reveals different cellular functions for FGF and Dpp signaling in tracheal branching morphogenesis. Dev. Cell2, 677–683 (2002). CASPubMed Google Scholar
Shim, K., Blake, K.J., Jack, J. & Krasnow, M.A. The Drosophila ribbon gene encodes a nuclear BTB domain protein that promotes epithelial migration and morphogenesis. Development128, 4923–4933 (2001). CASPubMed Google Scholar
O'Brien, L.E., Zegers, M.M. & Mostov, K.E. Opinion: Building epithelial architecture: insights from three-dimensional culture models. Nature Rev. Mol. Cell Biol.3, 531–537 (2002). CAS Google Scholar
Lipschutz, J.H. et al. Exocyst is involved in cystogenesis and tubulogenesis and acts by modulating synthesis and delivery of basolateral plasma membrane and secretory proteins. Mol. Biol. Cell11, 4259–4275 (2000). CASPubMedPubMed Central Google Scholar
Pollack, A.L., Runyan, R.B. & Mostov, K.E. Morphogenetic mechanisms of epithelial tubulogenesis: MDCK cell polarity is transiently rearranged without loss of cell–cell contact during scatter factor/hepatocyte growth factor-induced tubulogenesis. Dev. Biol.204, 64–79 (1998). CASPubMed Google Scholar
TerBush, D.R., Maurice, T., Roth, D. & Novick, P. The Exocyst is a multiprotein complex required for exocytosis in Saccharomyces cerevisiae. EMBO J.15, 6483–6494 (1996). CASPubMedPubMed Central Google Scholar
Grindstaff, K.K. et al. Sec6–8 complex is recruited to cell–cell contacts and specifies transport vesicle delivery to the basal-lateral membrane in epithelial cells. Cell93, 731–740 (1998). CASPubMed Google Scholar
Lipschutz, J.H. & Mostov, K.E. Exocytosis: the many masters of the Exocyst. Curr. Biol.12, R212–R214 (2002). CASPubMed Google Scholar
Jacinto, A., Woolner, S. & Martin, P. Dynamic analysis of dorsal closure in Drosophila: from genetics to cell biology. Dev. Cell3, 9–19 (2002). CASPubMed Google Scholar
Zeitlinger, J. & Bohmann, D. Thorax closure in Drosophila: involvement of Fos and the JNK pathway. Development126, 3947–3956 (1999). CASPubMed Google Scholar
Glise, B., Bourbon, H. & Noselli, S. hemipterous encodes a novel Drosophila MAP kinase kinase, required for epithelial cell sheet movement. Cell83, 451–461 (1995). CASPubMed Google Scholar
Riesgo-Escovar, J.R., Jenni, M., Fritz, A. & Hafen, E. The Drosophila Jun-N-terminal kinase is required for cell morphogenesis but not for DJun-dependent cell fate specification in the eye. Genes Dev.10, 2759–2768 (1996). CASPubMed Google Scholar
Sluss, H.K., Han, Z., Barrett, T., Davis, R.J. & Ip, Y.T. A JNK signal transduction pathway that mediates morphogenesis and an immune response in Drosophila. Genes Dev.10, 2745–2758 (1996). CASPubMed Google Scholar
Halsell, S.R., Chu, B.I. & Kiehart, D.P. Genetic analysis demonstrates a direct link between rho signaling and nonmuscle myosin function during Drosophila morphogenesis. Genetics155, 1253–1265 (2000). CASPubMedPubMed Central Google Scholar
Mizuno, T., Tsutsui, K. & Nishida, Y. Drosophila myosin phosphatase and its role in dorsal closure. Development129, 1215–1223 (2002). CASPubMed Google Scholar
Hakeda-Suzuki, S. et al. Rac function and regulation during Drosophila development. Nature416, 438–442 (2002). CASPubMed Google Scholar
Jacinto, A. et al. Dynamic actin-based epithelial adhesion and cell matching during Drosophila dorsal closure. Curr. Biol.10, 1420–1426 (2000). CASPubMed Google Scholar
Young, P.E., Richman, A.M., Ketchum, A.S. & Kiehart, D.P. Morphogenesis in Drosophila requires nonmuscle myosin heavy chain function. Genes Dev.7, 29–41 (1993). CASPubMed Google Scholar
Kiehart, D.P., Galbraith, C.G., Edwards, K.A., Rickoll, W.L. & Montague, R.A. Multiple forces contribute to cell sheet morphogenesis for dorsal closure in Drosophila. J. Cell Biol.149, 471–490 (2000). CASPubMedPubMed Central Google Scholar
Arquier, N., Perrin, L., Manfruelli, P. & Semeriva, M. The Drosophila tumor suppressor gene lethal(2) giant larvae is required for the emission of the Decapentaplegic signal. Development128, 2209–2220 (2001). CASPubMed Google Scholar
Kaltschmidt et al. Planar polarity and actin dynamics in the epidermis of Drosophila. Nature Cell Biol. (in the press).
Wallingford, J.B., Fraser, S.E. & Harland, R.M. Convergent extension: the molecular control of polarized cell movement during embryonic development. Dev. Cell2, 695–706 (2002). CASPubMed Google Scholar
Wallingford, J.B. et al. Dishevelled controls cell polarity during Xenopus gastrulation. Nature405, 81–85 (2000). CASPubMed Google Scholar
Munro, E.M. & Odell, G. Morphogenetic pattern formation during ascidian notochord formation is regulative and highly robust. Development129, 1–12 (2002). CASPubMed Google Scholar
Munro, E.M. & Odell, G.M. Polarized basolateral cell motility underlies invagination and convergent extension of the ascidian notochord. Development129, 13–24 (2002). CASPubMed Google Scholar
Irvine, K.D. & Wieschaus, E. Cell intercalation during Drosophila germband extension and its regulation by pair-rule segmentation genes. Development120, 827–841 (1994). CASPubMed Google Scholar
Brown, S. & Castelli-Gair Hombria, J. Drosophila grain encodes a GATA transcription factor required for cell rearrangement during morphogenesis. Development127, 4867–4876 (2000). CASPubMed Google Scholar
Hu, N. & Castelli-Gair, J. Study of the posterior spiracles of Drosophila as a model to understand the genetic and cellular mechanisms controlling morphogenesis. Dev. Biol.214, 197–210 (1999). CASPubMed Google Scholar
Tree, D.R., Ma, D. & Axelrod, J.D. A three-tiered mechanism for regulation of planar cell polarity. Semin. Cell Dev. Biol.13, 217–224 (2002). CASPubMed Google Scholar
Gho, M. & Schweisguth, F. Frizzled signalling controls orientation of asymmetric sense organ precursor cell divisions in Drosophila. Nature393, 178–181 (1998). CASPubMed Google Scholar
Axelrod, J.D. Unipolar membrane association of Dishevelled mediates Frizzled planar cell polarity signaling. Genes Dev.15, 1182–1187 (2001). CASPubMedPubMed Central Google Scholar
Strutt, D.I., Weber, U. & Mlodzik, M. The role of RhoA in tissue polarity and Frizzled signalling. Nature387, 292–295 (1997). CASPubMed Google Scholar
Habas, R., Kato, Y. & He, X. Wnt/Frizzled activation of Rho regulates vertebrate gastrulation and requires a novel Formin homology protein Daam1. Cell107, 843–54 (2001). CASPubMed Google Scholar
Lecuit, T.S., R. and Wieschaus, E. slam encodes a developmental regulator of polarized membrane growth during cleavage of the Drosophila embryo. Dev. Cell2, 425–436 (2002). CASPubMed Google Scholar
Jarrett, O., Stow, J.L., Yap, A.S. & Key, B. Dynamin-dependent endocytosis is necessary for convergent-extension movements in Xenopus animal cap explants. Int. J. Dev. Biol.46, 467–473 (2002). CASPubMed Google Scholar