FGF Signaling Regulates Cytoskeletal Remodeling during Epithelial Morphogenesis

Current Biology

Volumn 18, Issue 13, 2008, Pages 976-981

  Sai, XiaoRei ^a   Ladher, Raj K ^a  

^a RIKEN KOBE INSTITUTE   (Japan)

Author keywords

DEVBIO; SIGNALING

Indexed keywords

ACTIN; FIBROBLAST GROWTH FACTOR; MYOSIN II; PHOSPHOLIPASE C GAMMA;

ANIMAL; ARTICLE; CHICK EMBRYO; CYTOSKELETON; ECTODERM; ENZYME ACTIVATION; EPITHELIUM; INNER EAR; METABOLISM; MORPHOGENESIS; PHYSIOLOGY; PRENATAL DEVELOPMENT;

ACTINS; ANIMALS; CHICK EMBRYO; CYTOSKELETON; EAR, INNER; ECTODERM; ENZYME ACTIVATION; EPITHELIUM; FIBROBLAST GROWTH FACTORS; MORPHOGENESIS; MYOSIN TYPE II; PHOSPHOLIPASE C GAMMA;

EID: 45849123181     PISSN: 09609822     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cub.2008.05.049     Document Type: Article

References (38)

1. Jacinto A., and Baum B. Actin in development. Mech. Dev. 120 (2003) 1337-1349
2. Haigo S.L., Hildebrand J.D., Harland R.M., and Wallingford J.B. Shroom induces apical constriction and is required for hingepoint formation during neural tube closure. Curr. Biol. 13 (2003) 2125-2137
3. Copp A.J. Neurulation in the cranial region-normal and abnormal. J. Anat. 207 (2005) 623-635
4. Pilot F., and Lecuit T. Compartmentalized morphogenesis in epithelia: from cell to tissue shape. Dev. Dyn. 232 (2005) 685-694
5. Ladher R.K., Anakwe K.U., Gurney A.L., Schoenwolf G.C., and Francis-West P.H. Identification of synergistic signals initiating inner ear development. Science 290 (2000) 1965-1967
6. Wright T.J., and Mansour S.L. Fgf3 and Fgf10 are required for mouse otic placode induction. Development 130 (2003) 3379-3390
7. Meier S. Development of the embryonic chick otic placode. I. Light microscopic analysis. Anat. Rec. 191 (1978) 447-458
8. Hilfer S.R., Esteves R.A., and Sanzo J.F. Invagination of the otic placode: normal development and experimental manipulation. J. Exp. Zool. 251 (1989) 253-264
9. Alvarez I.S., and Navascués J. Shaping, invagination, and closure of the chick embryo otic vesicle: scanning electron microscopic and quantitative study. Anat. Rec. 228 (1990) 315-326
10. Groves A.K., and Bronner-Fraser M. Competence, specification and commitment in otic placode induction. Development 127 (2000) 3489-3499
11. Kil S.H., Streit A., Brown S.T., Agrawal N., Collazo A., Zile M.H., and Groves A.K. Distinct roles for hindbrain and paraxial mesoderm in the induction and patterning of the inner ear revealed by a study of vitamin-A-deficient quail. Dev. Biol. 285 (2005) 252-271
12. Dawes-Hoang R.E., Parmar K.M., Christiansen A.E., Phelps C.B., Brand A.H., and Wieschaus E.F. Folded gastrulation, cell shape change and the control of myosin localization. Development 132 (2005) 4165-4178
13. Lee J.Y., and Harland R.M. Actomyosin contractility and microtubules drive apical constriction in Xenopus bottle cells. Dev. Biol. 311 (2007) 40-52
14. Jacinto A., Woolner S., and Martin P. Dynamic analysis of dorsal closure in Drosophila: from genetics to cell biology. Dev. Cell 3 (2002) 9-19
15. Colas J.F., and Schoenwolf G.C. Towards a cellular and molecular understanding of neurulation. Dev. Dyn. 221 (2001) 117-145
16. Cooper J.A. Effects of cytochalasin and phalloidin on actin. J. Cell Biol. 105 (1987) 1473-1478
17. Bubb M.R., Spector I., Beyer B.B., and Fosen K.M. Effects of jasplakinolide on the kinetics of actin polymerization. An explanation for certain in vivo observations. J. Biol. Chem. 275 (2000) 5163-5170
18. Mohammadi M., McMahon G., Sun L., Tang C., Hirth P., Yeh B.K., Hubbard S.R., and Schlessinger J. Structures of the tyrosine kinase domain of fibroblast growth factor receptor in complex with inhibitors. Science 276 (1997) 955-960
19. Martin K., and Groves A.K. Competence of cranial ectoderm to respond to Fgf signaling suggests a two-step model of otic placode induction. Development 133 (2006) 877-887
20. Kouhara H., Hadari Y.R., Spivak-Kroizman T., Schilling J., Bar-Sagi D., Lax I., and Schlessinger J. A lipid-anchored Grb2-binding protein that links FGF-receptor activation to the Ras/MAPK signaling pathway. Cell 89 (1997) 693-702
21. Burgess W.H., Dionne C.A., Kaplow J., Mudd R., Friesel R., Zilberstein A., Schlessinger J., and Jaye M. Characterization and cDNA cloning of phospholipase C-gamma, a major substrate for heparin-binding growth factor 1 (acidic fibroblast growth factor)-activated tyrosine kinase. Mol. Cell. Biol. 10 (1990) 4770-4777
22. Ono S. Mechanism of depolymerization and severing of actin filaments and its significance in cytoskeletal dynamics. Int. Rev. Cytol. 258 (2007) 1-82
23. Medeiros N.A., Burnette D.T., and Forscher P. Myosin II functions in actin-bundle turnover in neuronal growth cones. Nat. Cell Biol. 8 (2006) 215-226
24. Murthy K., and Wadsworth P. Myosin-II-dependent localization and dynamics of F-actin during cytokinesis. Curr. Biol. 15 (2005) 724-731
25. Guha M., Zhou M., and Wang Y.L. Cortical actin turnover during cytokinesis requires myosin II. Curr. Biol. 15 (2005) 732-736
26. Ishikawa R., Sakamoto T., Ando T., Higashi-Fujime S., and Kohama K. Polarized actin bundles formed by human fascin-1: their sliding and disassembly on myosin II and myosin V in vitro. J. Neurochem. 87 (2003) 676-685
27. Haviv L., Gillo D., Backouche F., and Bernheim-Groswasser A. A cytoskeletal demolition worker: myosin II acts as an actin depolymerization agent. J. Mol. Biol. 375 (2008) 325-330
28. Schliwa M., and Woehlke G. Molecular motors. Nature 422 (2003) 759-765
29. Straight A.F., Cheung A., Limouze J., Chen I., Westwood N.J., Sellers J.R., and Mitchison T.J. Dissecting temporal and spatial control of cytokinesis with a myosin II Inhibitor. Science 299 (2003) 1743-1747
30. Saitoh M., Ishikawa T., Matsushima S., Naka M., and Hidaka H. Selective inhibition of catalytic activity of smooth muscle myosin light chain kinase. J. Biol. Chem. 262 (1987) 7796-7801
31. Sadler T.W., Greenberg D., Coughlin P., and Lessard J.L. Actin distribution patterns in the mouse neural tube during neurulation. Science 215 (1982) 172-174
32. Morriss-Kay G., and Tuckett F. The role of microfilaments in cranial neurulation in rat embryos: effects of short-term exposure to cytochalasin D. J. Embryol. Exp. Morphol. 88 (1985) 333-348
33. van Straaten H.W., Sieben I., and Hekking J.W. Multistep role for actin in initial closure of the mesencephalic neural groove in the chick embryo. Dev. Dyn. 224 (2002) 103-108
34. Fox D.T., and Peifer M. Abelson kinase (Abl) and RhoGEF2 regulate actin organization during cell constriction in Drosophila. Development 134 (2007) 567-578
35. Nishimura T., and Takeichi M. Shroom3-mediated recruitment of Rho kinases to the apical cell junctions regulates epithelial and neuroepithelial planar remodeling. Development 135 (2008) 1493-1502
36. Lecuit T., and Lenne P.F. Cell surface mechanics and the control of cell shape, tissue patterns and morphogenesis. Nat. Rev. Mol. Cell Biol. 8 (2007) 633-644
37. Mansour S.L., and Schoenwolf G.C. Morphogenesis of the inner ear. In: Kelley M.W., Wu D.K., Popper A.N., and Fay R.R. (Eds). Development of the Inner Ear (2005), Springer, New York 43-84
38. Hoch R.V., and Soriano P. Context-specific requirements for Fgfr1 signaling through Frs2 and Frs3 during mouse development. Development 133 (2006) 663-673