BDNF-Akt-Bcl2 antiapoptotic signaling pathway is compromised in the brain of autistic subjects

Although the pathogenesis of autism is not understood, emerging evidence points to apoptotic mechanisms being involved in this disorder. However, it is not known whether apoptosis signaling is deregulated in the brain of autistic subjects. This study investigates how the apoptosis‐related proteins a...

Full description

Saved in:
Bibliographic Details
Published inJournal of neuroscience research Vol. 88; no. 12; pp. 2641 - 2647
Main Authors Sheikh, Ashfaq M., Malik, Mazhar, Wen, Guang, Chauhan, Abha, Chauhan, Ved, Gong, Cheng-Xin, Liu, Fei, Brown, William T., Li, Xiaohong
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.09.2010
Subjects
Online AccessGet full text
ISSN0360-4012
1097-4547
1097-4547
DOI10.1002/jnr.22416

Cover

More Information
Summary:Although the pathogenesis of autism is not understood, emerging evidence points to apoptotic mechanisms being involved in this disorder. However, it is not known whether apoptosis signaling is deregulated in the brain of autistic subjects. This study investigates how the apoptosis‐related proteins are regulated in the autistic brain. Our studies show that Bcl2 is significantly decreased, whereas the expression of p53 is increased, in the brain of autistic subjects in comparison with age‐matched controls. We also found that the expression and phosphorylation/activation of Akt kinase that regulates Bcl2 are significantly decreased in the autistic brain. The down‐regulation of Akt may result from a decreased concentration of brain‐derived neurotrophic factor (BDNF), the growth factor that modulates Akt activities. These results suggest that down‐regulation of the BDNF‐Akt‐Bcl2 antiapoptotic signaling pathway in the autistic brain could be one of the underlying mechanisms responsible for the pathogenesis of autism. © 2010 Wiley‐Liss, Inc.
Bibliography:ark:/67375/WNG-7CZCTHC6-V
ArticleID:JNR22416
istex:3A428A2005B6C9A2A93E9F0B3D19D503B01D5421
New York State Office of Mental Retardation and Developmental Disabilities
ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Article-4
ObjectType-Report-1
ObjectType-Article-2
ObjectType-Feature-1
ISSN:0360-4012
1097-4547
1097-4547
DOI:10.1002/jnr.22416