Estrogen synthesis in the male brain triggers development of the avian song control pathway in vitro

Sexual differentiation of the brain is determined in part by steroids such as estrogen, which are generally assumed to arise from the gonads. Here we show that estrogens are produced autonomously in cultured juvenile male zebra finch brain slices, and this brain-derived estrogen is both necessary and sufficient to trigger formation in vitro of a key male-specific synaptic connection in the telencephalic song control circuit. Male-like development was stimulated in female slices cultured with male slices or exposed to estrogen, and estrogen antagonists inhibited song circuit development in slices of either sex. These results reveal a new mode of sex-specific neural development, induced not by differential exposure to gonadal steroids, but rather by differential synthesis of steroids in the brain.

[1]  A. Arnold,et al.  Developmental Regulation of the Distribution of Aromatase- and Estrogen-Receptor- mRNA-Expressing Cells in the Zebra Finch Brain , 2000, Developmental Neuroscience.

[2]  Richard Mooney,et al.  Sensitive periods and circuits for learned birdsong , 1999, Current Opinion in Neurobiology.

[3]  A. Arnold,et al.  Functional testicular tissue does not masculinize development of the zebra finch song system. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[4]  A. Arnold,et al.  Tamoxifen's effects on the zebra finch song system are estrogenic, not antiestrogenic. , 1991, Journal of neurobiology.

[5]  A. Arnold,et al.  3 beta-hydroxysteroid dehydrogenase/isomerase and aromatase activity in primary cultures of developing zebra finch telencephalon: dehydroepiandrosterone as substrate for synthesis of androstenedione and estrogens. , 1996, General and comparative endocrinology.

[6]  J. Balthazart,et al.  Sex- and age-related differences in the activity of testosterone-metabolizing enzymes in microdissected nuclei of the zebra finch brain , 1990, Brain Research.

[7]  Stephen J. Smith,et al.  The Dynamics of Dendritic Structure in Developing Hippocampal Slices , 1996, The Journal of Neuroscience.

[8]  M. Gahr,et al.  Estrogen-inducible, sex-specific expression of brain-derived neurotrophic factor mRNA in a forebrain song control nucleus of the juvenile zebra finch. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[9]  A. Arnold,et al.  Fadrozole: a potent and specific inhibitor of aromatase in the zebra finch brain. , 1994, General and comparative endocrinology.

[10]  V. Jordan,et al.  Basic guide to the mechanisms of antiestrogen action. , 1998, Pharmacological reviews.

[11]  A. Arnold,et al.  Sexual differentiation of the zebra finch song system: positive evidence, negative evidence, null hypotheses, and a paradigm shift. , 1997, Journal of neurobiology.

[12]  M. Gahr,et al.  The Sexually Dimorphic Expression of Androgen Receptors in the Song Nucleus Hyperstriatalis Ventrale Pars Caudale of the Zebra Finch Develops Independently of Gonadal Steroids , 1999, The Journal of Neuroscience.

[13]  A. Arnold,et al.  Circulating estrogens in a male songbird originate in the brain. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[14]  M. G. Honig,et al.  Fluorescent carbocyanine dyes allow living neurons of identified origin to be studied in long-term cultures , 1986, The Journal of cell biology.

[15]  M. Gurney,et al.  Hormone-Induced Sexual Differentiation of Brain and Behavior in Zebra Finches , 1980, Science.

[16]  E. Nordeen,et al.  Sexual differentiation of androgen accumulation within the zebra finch brain through selective cell loss and addition , 1987, The Journal of comparative neurology.

[17]  H. Gainer,et al.  Characterization of the suprachiasmatic nucleus in organotypic slice explant cultures , 1993, Microscopy research and technique.

[18]  B. Schlinger Sex steroids and their actions on the birdsong system. , 1997, Journal of neurobiology.

[19]  D Margoliash,et al.  An introduction to birdsong and the avian song system. , 1997, Journal of neurobiology.

[20]  S. Bottjer,et al.  Axonal connections of the High Vocal Center and surrounding cortical regions in juvenile and adult male zebra finches , 1998, The Journal of comparative neurology.

[21]  J. Wingfield,et al.  Sex differences in plasma concentrations of steroids during the sensitive period for brain differentiation in the zebra finch. , 1984, The Journal of endocrinology.

[22]  A. Arnold,et al.  Post-hatching inhibition of aromatase activity does not alter sexual differentiation of the zebra finch song system , 1994, Brain Research.

[23]  A. Arnold,et al.  Aromatase and 5 beta-reductase activity in cultures of developing zebra finch brain: an investigation of sex and regional differences. , 1995, Journal of neurobiology.

[24]  C. Toran-Allerand Organotypic culture of the developing cerebral cortex and hypothalamus: Relevance to sexual differentiation , 1991, Psychoneuroendocrinology.

[25]  Colin Blakemore,et al.  Development of Signals Influencing the Growth and Termination of Thalamocortical Axons in Organotypic Culture , 1999, Experimental Neurology.

[26]  S. Bottjer Building a bird brain: Sculpting neural circuits for a learned behavior , 1997 .

[27]  A. Arnold,et al.  Antiestrogens fail to prevent the masculine ontogeny of the zebra finch song system. , 1990, General and comparative endocrinology.

[28]  A. Arnold,et al.  Plasma sex steroids and tissue aromatization in hatchling zebra finches: implications for the sexual differentiation of singing behavior. , 1992, Endocrinology.

[29]  A. Arnold,et al.  Brain is the major site of estrogen synthesis in a male songbird. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[30]  S. M. Breedlove,et al.  Sexual Differentiation of the Vertebrate Brain: Principles and Mechanisms , 1998, Frontiers in Neuroendocrinology.

[31]  E. Adkins-Regan,et al.  Behavior of male and female zebra finches treated with an estrogen synthesis inhibitor as nestlings , 1996 .

[32]  A. S. Clark,et al.  Aromatase in the Cerebral Cortex, Hippocampus, and Mid-Brain: Ontogeny and Developmental Implications , 1994, Molecular and Cellular Neuroscience.

[33]  Meharvan Singh,et al.  Novel Mechanisms of Estrogen Action in the Brain: New Players in an Old Story , 1999, Frontiers in Neuroendocrinology.

[34]  D. Muller,et al.  A simple method for organotypic cultures of nervous tissue , 1991, Journal of Neuroscience Methods.

[35]  F. Nottebohm,et al.  Central control of song in the canary, Serinus canarius , 1976, The Journal of comparative neurology.

[36]  E. Adkins-Regan,et al.  Sex steroid levels in developing and adult male and female zebra finches (Poephila guttata). , 1990, General and comparative endocrinology.

[37]  G. Ball,et al.  EFFECTS OF THE AROMATASE INHIBITOR R76713 ON SEXUAL DIFFERENTIATION OF BRAIN AND BEHAVIOR IN ZEBRA FINCHES , 1994 .

[38]  D. Vicario,et al.  Early estrogen treatment of female zebra finches masculinizes the brain pathway for learned vocalizations. , 1991, Journal of neurobiology.

[39]  Fiber outgrowth and pathfinding in the developing auditory brainstem. , 1995, Brain research. Developmental brain research.

[40]  D. Vicario,et al.  Early estrogen treatment alone causes female zebra finches to produce learned, male-like vocalizations. , 1991, Journal of neurobiology.

[41]  M. Konishi,et al.  Developmental changes in estrogen-sensitive neurons in the forebrain of the zebra finch. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[42]  B. Schlinger,et al.  Neuronal and non-neuronal aromatase in primary cultures of developing zebra finch telencephalon , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[43]  S. Goldman,et al.  In vitro neurogenesis by neuronal precursor cells derived from the adult songbird brain , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[44]  R. Robertson,et al.  Development of AChE-positive neuronal projections from basal forebrain to cerebral cortex in organotypic tissue slice cultures. , 1992, Brain research. Developmental brain research.

[45]  R. Mooney,et al.  Waiting periods versus early innervation: the development of axonal connections in the zebra finch song system , 1994, Journal of Neuroscience.

[46]  Masakazu Konishi,et al.  Neuronal growth, atrophy and death in a sexually dimorphic song nucleus in the zebra finch brain , 1985, Nature.