Origins of inner ear sensory organs revealed by fate map and time-lapse analyses

Developmental Biology

Volumn 233, Issue 2, 2001, Pages 365-379

  Kil, Sung Hee ^a   Collazo, Andres ^a  

^a HOUSE EAR INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BONE MORPHOGENETIC PROTEIN 4; TRANSFORMING GROWTH FACTOR BETA;

ANIMAL CELL; ARTICLE; CELL FATE; CHICKEN; GENE EXPRESSION REGULATION; INNER EAR; MICROSCOPIC ANATOMY; NERVE CELL DIFFERENTIATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; XENOPUS LAEVIS;

ANURA; GALLUS GALLUS; XENOPUS LAEVIS;

EID: 0035873409     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1006/dbio.2001.0211     Document Type: Article

References (36)

1. Adam J., Myat A., Le Roux I., Eddison M., Henrique D., Ish-Horowicz D., Lewis J. Cell fate choices and the expression of Notch, Delta and Serrate homologues in the chick inner ear: Parallels with Drosophila sense-organ development. Development. 125:1998;4645-4654.
2. Brigande J. V., Iten L. E., Fekete D. M. A fate map of chick otic cup reveals lineage boundaries in the dorsal otocyst. Dev. Biol. 227:2000;256-270.
3. Chang W., Nunes F. D., De Jesus-Escobar J. M., Harland R., Wu D. K. Ectopic noggin blocks sensory and nonsensory organ morphogenesis in the chicken inner ear. Dev. Biol. 216:1999;369-381.
4. Collazo A., Fraser S. E. Lateral line development in mutant zebrafish. Assoc. Res. Otolaryngol. Abs. 689:1998;173.
5. Collazo A., Fraser S. E., Mabee P. M. A dual embryonic origin for vertebrate mechanoreceptors. Science. 264:1994;426-430.
6. Fekete D. M. Cell fate specification in the inner-ear. Curr. Opin. Neurobiol. 6:1996;533-541.
7. Fekete D. M. Development of the vertebrate ear: Insights from knockouts and mutants. Trends Neurosci. 22:1999;263-269.
8. Fekete D. M., Muthukumar S., Karagogoes D. Hair cells and supporting cells share a common progenitor in the avian inner ear. J. Neurosci. 18:1998;7811-7821.
9. Fritzsch B., Barald K. F., Lomax M. I. Early embryology of the vertebrate ear. Rubel E. W., Popper A. N., Fay R. R. Development of the Auditory System. 1998;80-145 Springer, New York.
10. Gerlach L. M., Hutson M. R., Germiller J. A., Nguyen-Luu D., Victor J. C., Barald K. F. Addition of the BMP4 antagonist, noggin, disrupts avian inner ear development. Development. 127:2000;45-54.
11. Goldberg M. E., Hudspeth A. J. The vestibular system. Kandel E. R., Schwartz J. H., Jessell T. M. Principles of Neural Science. 2000;801-815 McGraw-Hill, New York.
12. Haddon C. H., Lewis J. Early ear development in the embryo of the zebrafish Danio rerio. J. Comp. Neurol. 365:1996;113-128.
13. Harland R., Gerhart J. Formation and function of Spemanns organizer. Annu. Rev. Cell Dev. Biol. 13:1997;611-667.
14. Harland R. M. In-situ hybridization: An improved whole-mount method For Xenopus embryos. Methods Cell Biol. 36:1991;685-695.
15. Harrison R. G. Relations of symmetry in the developing ear of Amblystoma punctatum. Proc. Natl. Acad. Sci. USA. 22:1936;238-247.
16. Hausen P., Riebesell M. The Early Development of Xenopus laevis. 1991;Springer-Verlag, New York.
17. Hemmati-Brivanlou A., Thomsen G. H. Ventral mesodermal patterning in Xenopus embryos: Expression patterns and activities of Bmp-2 and Bmp-4. Dev. Genet. 17:1995;78-89.
18. Henrique D., Adam J., Myat A., Chitnis A., Lewis J., Ishhorowicz D. Expression of a Delta-homolog in prospective neurons in the chick. Nature. 375:1995;787-790.
19. Hudspeth A. J. How the ears works work. Nature. 341:1989;397-404.
20. Knecht A. K., Good P. J., Dawid I. B., Harland R. M. Dorsal-ventral patterning and differentiation of Noggin-induced neural tissue in the absence of mesoderm. Development. 121:1995;1927-1935.
21. Knowlton V. Y. Correlation of the development of membranous and bony labyrinths, acoustics ganglia, nerves, and brain centers of chick embryos. J. Morphol. 121:1967;179-208.
22. Lewis E. R., Narins P. M. The acoustic periphery of amphibians: Anatomy and physiology. Fay R. R., Popper A. N. Comparative Hearing: Fish and Amphibians. 1999;101-154 Springer-Verlag, New York.
23. Li C. W., Van de Water T. R., Ruben R. J. The fate mapping of the eleventh and twelfth day mouse otocyst: An in vitro study of the sites of origin of the embryonic inner ear sensory structures. J. Morphol. 157:1978;249-268.
24. Morsli H., Choo D., Ryan A., Johnson R., Wu D. K. Development of the mouse inner ear and origin of its sensory organs. J. Neurosci. 18:1998;3327-3335.
25. Nieuwkoop P. D., Faber J. Normal Table of Xenopus laevis (Daudin). 1967;North-Holland, Amsterdam.
26. Oh S. H., Johnson R., Wu D. K. Differential expression of bone morphogenetic proteins in the developing vestibular and auditory sensory organs. J. Neurosci. 16:1996;6463-6475.
27. Romer A. S., Parsons T. S. The Vertebrate Body. 1977;Saunders, Philadelphia.
28. Sher A. E. The embryonic and postnatal development of the inner ear of the mouse. Acta Otolayngol. 285:1972;1-77.
29. Strahle U., Blader P., Adam J., Ingham P. W. A simple and efficient procedure for non-isotopic in situ hybridization to sectioned material. Trends Genet. 10:1994;75-76.
30. Torres M., Giraldez F. The development of the vertebrate inner-ear. Mech. Dev. 71:1998;5-21.
31. Vize P. D., Melton D. A., Hemmatibrivanlou A., Harland R. M. Assays for gene-function in developing Xenopus-embryos. Methods Cell Biol. 36:1991;367-387.
32. Wilkinson D. E. In Situ Hybridisation: A Practical Approach. 1992;IRL Press, Oxford.
33. Woo K., Shih J., Fraser S. E. Fate maps of the zebrafish embryo. Curr. Opin. Genet. Dev. 5:1995;439-443.
34. Wu D. K., Nunes F. D., Choo D. Axial specification for sensory organs versus nonsensory structures of the chicken inner-ear. Development. 125:1998;11-20.
35. Wu D. K., Oh S. H. Sensory organ generation in the chick inner-ear. J. Neurosci. 16:1996;6454-6462.
36. Yntema C. L. Ear and nose. Willier B. H., Weiss P. A., Hamburger V. Analysis of Development. 1955;415-428 Saunders, Philadelphia.