Literature DB >> 7996194

Neuronal and non-neuronal aromatase in primary cultures of developing zebra finch telencephalon.

B A Schlinger1, S Amur-Umarjee, P Shen, A T Campagnoni, A P Arnold.   

Abstract

Estrogenic metabolites of circulating androgens have important effects on the organization and activation of neural circuits controlling reproductive behavior and physiology in males of many vertebrate species. Previous studies indicate that aromatase, the enzyme that converts androgens to estrogens, is expressed most abundantly in neurons in limbic brain regions. Songbirds are unique in that aromatase is expressed at unusually high levels throughout the telencephalon of both males and females. We assume that estrogens formed in the telencephalon itself masculinize neural circuits controlling song, since the brain is a major source of circulating estrogens in adult males. However, the cellular localization of telencephalic aromatase in songbirds remains unknown. We have established primary cultures from telencephalons of developing zebra finches and found aromatase activity (conversion of 3H-androstenedione or 3H-testosterone to 3H-estrone plus 3H-estradiol) at some of the highest levels reported for brain tissue of any species. Both neurons and glia were identified in these cultures based on cell morphology and labeling by specific immunohistochemical markers. However, when culture conditions were manipulated to reduce the incidence of either neurons or glia by varying the age of cultures or their plating density, treating with the neurotoxin kainic acid, physically shaking off loosely attached neurons, or preparing cultures in media that encouraged enrichment of neurons, high levels of aromatase persisted. Furthermore, Northern blot analysis of total RNA extracted from enriched neuronal or glial cultures indicated the presence of aromatase mRNA in both cell preparations. In situ hybridization with a zebra finch aromatase cDNA probe conjugated to digoxigenin showed the cultures contained darkly labeled neurons and lightly labeled non-neuronal cells, presumably astrocytes. We conclude that aromatase is expressed in both neuronal and non-neuronal cells in these cultures, suggesting that both cell types may also express the enzyme in vivo. The presence of aromatase outside of neurons suggests that glia may be targets of estrogen action or that glia may supply some estrogen to the estrogen-sensitive neural circuits in this species.

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Year:  1994        PMID: 7996194      PMCID: PMC6576881     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  25 in total

1.  Females of an African cichlid fish display male-typical social dominance behavior and elevated androgens in the absence of males.

Authors:  Suzy C P Renn; Eleanor J Fraser; Nadia Aubin-Horth; Brian C Trainor; Hans A Hofmann
Journal:  Horm Behav       Date:  2012-01-18       Impact factor: 3.587

Review 2.  Recent advances in behavioral neuroendocrinology: insights from studies on birds.

Authors:  James L Goodson; Colin J Saldanha; Thomas P Hahn; Kiran K Soma
Journal:  Horm Behav       Date:  2005-11       Impact factor: 3.587

3.  Inhibition of hippocampal aromatization impairs spatial memory performance in a male songbird.

Authors:  David J Bailey; Chunqi Ma; Kiran K Soma; Colin J Saldanha
Journal:  Endocrinology       Date:  2013-10-08       Impact factor: 4.736

4.  Songbirds: A novel perspective on estrogens and the aging brain.

Authors:  Barney A Schlinger; Colin J Saldanha
Journal:  Age (Dordr)       Date:  2006-02-17

5.  Activities of 3beta-HSD and aromatase in slices of developing and adult zebra finch brain.

Authors:  Helen Tam; Barney A Schlinger
Journal:  Gen Comp Endocrinol       Date:  2006-08-21       Impact factor: 2.822

6.  Anatomical distribution and cellular basis for high levels of aromatase activity in the brain of teleost fish: aromatase enzyme and mRNA expression identify glia as source.

Authors:  P M Forlano; D L Deitcher; D A Myers; A H Bass
Journal:  J Neurosci       Date:  2001-11-15       Impact factor: 6.167

7.  Aggressive interactions rapidly increase androgen synthesis in the brain during the non-breeding season.

Authors:  Devaleena S Pradhan; Amy E M Newman; Douglas W Wacker; John C Wingfield; Barney A Schlinger; Kiran K Soma
Journal:  Horm Behav       Date:  2010-01-29       Impact factor: 3.587

8.  Genomic and neural analysis of the estradiol-synthetic pathway in the zebra finch.

Authors:  Sarah E London; David F Clayton
Journal:  BMC Neurosci       Date:  2010-04-01       Impact factor: 3.288

Review 9.  Neuroprotective actions of brain aromatase.

Authors:  Colin J Saldanha; Kelli A Duncan; Bradley J Walters
Journal:  Front Neuroendocrinol       Date:  2009-05-18       Impact factor: 8.606

10.  Avian axons undergo Wallerian degeneration after injury and stress.

Authors:  John C Bramley; Samantha V A Collins; Karen B Clark; William J Buchser
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2016-09-10       Impact factor: 1.836

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