The goal of our research program is to understand the cellular and molecular events that control sexual differentiation of nerves and muscles. In Xenopus laevis, masculinization of the vocal organ is controlled by gonadal steroids acting through intracellular receptor proteins. We are investigating how secretion of androgenic hormones produces increases in muscle fiber number in developing larynx.
Our aims are to discover when androgens act, what cell types are responsible and how the very high androgen receptor protein levels in larynx are regulated. We will measure serum hormone levels during very early development using radioimmunoassay. Androgen action will be blocked at different developmental stages and effects on muscle fiber number assayed. The distribution of androgen receptor containing laryngeal cells will be studied in tissue culture to follow androgen receptor expression at the single cell level. Effects of androgen on myoblast survival, proliferation and fusion will be assayed in vitro. Regulation of androgen receptor expression at the single cell level. Effects of androgen on myoblast survival, proliferation and fusion will be assayed in vitro. Regulation of androgen receptor expression at the messenger RNA level will be examined using Northern analyses and in situ hybridization. Androgen secretion during development controls expression of the masculine phenotype in most vertebrates. Muscles and nerves are targets for androgen action because they contain specific receptor proteins. Clinical disorders associated with abnormalities in androgen secretion or receptor expression include pseudohermaphroditism, testicular feminization, neuroendocrine and muscular abnormalities and alterations in gender identity. An understanding of the basic mechanisms for androgen action can be obtained from studies in animal models and is essential in understanding the basis of human clinical disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
2R01NS019949-07
Application #
3400085
Study Section
Neurology B Subcommittee 1 (NEUB)
Project Start
1983-07-01
Project End
1992-08-31
Budget Start
1989-09-25
Budget End
1990-08-31
Support Year
7
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Type
Graduate Schools
DUNS #
064931884
City
New York
State
NY
Country
United States
Zip Code
10027
Perez, J; Kelley, D B (1997) Androgen mitigates axotomy-induced decreases in calbindin expression in motor neurons. J Neurosci 17:7396-403
Kelley, D B (1997) Generating sexually differentiated songs. Curr Opin Neurobiol 7:839-43
Cohen, M A; Kelley, D B (1996) Androgen-induced proliferation in the developing larynx of Xenopus laevis is regulated by thyroid hormone. Dev Biol 178:113-23
Perez, J; Cohen, M A; Kelley, D B (1996) Androgen receptor mRNA expression in Xenopus laevis CNS: sexual dimorphism and regulation in laryngeal motor nucleus. J Neurobiol 30:556-68
Robertson, J C; Kelley, D B (1996) Thyroid hormone controls the onset of androgen sensitivity in the developing larynx of Xenopus laevis. Dev Biol 176:108-23
Perez, J; Kelley, D B (1996) Trophic effects of androgen: receptor expression and the survival of laryngeal motor neurons after axotomy. J Neurosci 16:6625-33
Kang, L; Marin, M; Kelley, D (1995) Androgen biosynthesis and secretion in developing Xenopus laevis. Gen Comp Endocrinol 100:293-307
Tobias, M L; Marin, M L; Kelley, D B (1993) The roles of sex, innervation, and androgen in laryngeal muscle of Xenopus laevis. J Neurosci 13:324-33
Fischer, L; Catz, D; Kelley, D (1993) An androgen receptor mRNA isoform associated with hormone-induced cell proliferation. Proc Natl Acad Sci U S A 90:8254-8
He, W W; Fischer, L M; Sun, S et al. (1990) Molecular cloning of androgen receptors from divergent species with a polymerase chain reaction technique: complete cDNA sequence of the mouse androgen receptor and isolation of androgen receptor cDNA probes from dog, guinea pig and clawed frog. Biochem Biophys Res Commun 171:697-704

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