17β-estradiol regulates the sexually dimorphic expression of bdnf and trkb proteins in the song system of juvenile zebra finches17β-estradiol调节的性别差异表达bdnf和trkb少年斑马雀歌系统中的蛋白质.pdfVIP
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17β-estradiol regulates the sexually dimorphic expression of bdnf and trkb proteins in the song system of juvenile zebra finches17β-estradiol调节的性别差异表达bdnf和trkb少年斑马雀歌系统中的蛋白质
17b-Estradiol Regulates the Sexually Dimorphic
Expression of BDNF and TrkB Proteins in the Song
System of Juvenile Zebra Finches
Yu Ping Tang*, Juli Wade
Neuroscience Program, Departments of Psychology and Zoology, Michigan State University, East Lansing, Michigan, United States of America
Abstract
Mature brain derived neurotrophic factor (BDNF) plays critical roles in development of brain structure and function,
including neurogenesis, axon growth, cell survival and processes associated with learning. Expression of this peptide is
regulated by estradiol (E2). The zebra finch song system is sexually dimorphic – only males sing and the brain regions
controlling song are larger and have more cells in males compared to females. Masculinization of this system is partially
mediated by E2, and earlier work suggests that BDNF with its high affinity receptor TrkB may also influence this
development. The present study evaluated expression of multiple forms of both BDNF and TrkB in the developing song
system in juvenile males and females treated with E2 or a vehicle control. Using immunohistochemistry and Western blot
analysis, BDNF was detected across the song nuclei of 25-day-old birds. Westerns allowed the pro- and mature forms of
BDNF to be individually identified, and proBDNF to be quantified. Several statistically significant effects of sex existed in
both the estimated total number of BDNF+ cells and relative concentration of proBDNF, varying across the regions and
methodologies. E2 modulated BDNF expression, although the specific nature of the regulation depended on brain region,
sex and the technique used. Similarly, TrkB (both truncated and full-length isoforms) was detected by Western blot in the
song system of juveniles of both sexes, and expression was regulated by E2. In the context
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