BDNF expression in lymphoblastoid cell lines carrying BDNF SNPs associated with bipolar disorder

被引:6
作者
Gao, Yonglin [1 ]
Galante, Mathew [1 ]
El-Mallakh, James [1 ]
Nurnberger, John I., Jr. [3 ]
Delamere, Nicholas A. [4 ]
Lei, Zhenmin [2 ]
El-Mallakh, Rif S. [1 ]
机构
[1] Univ Louisville, Sch Med, Dept Psychiat & Behav Sci, Mood Disorder Res Program, Louisville, KY 40292 USA
[2] Univ Louisville, Sch Med, Dept Obstet & Gynecol, Louisville, KY 40292 USA
[3] Indiana Univ Sch Med, Dept Psychiat, Indianapolis, IN USA
[4] Univ Arizona, Hlth Sci Ctr, Dept Physiol, Tucson, AZ USA
关键词
apoptosis; bipolar disorder; brain-derived neurotrophic factor; intracellular sodium; single nucleotide polymorphism; NEUROTROPHIC FACTOR; APOPTOSIS; SORTILIN;
D O I
10.1097/YPG.0b013e328353ae66
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objective To determine whether single nucleotide polymorphisms (SNPs) of the brain-derived neurotrophic factor (BDNF) that have been associated with bipolar illness are associated with physiological dysfunction. Methods Lymphoblastoid cell lines (n=30) obtained from bipolar I individuals carrying zero, one, or two copies of a BDNF SNP associated with bipolar illness (rs12273363) were utilized. Results Proapoptotic stressors of serum deprivation alone, or serum deprivation combined with the sodium ionophore, monensin, did not alter intracellular proBDNF. Monensin treatment increased mature-BDNF (mBDNF) protein levels (P<0.05). There were no differences related to the presence of SNP or copy number. Conclusion rs12273363 does not appear to have functional consequences that would involve its role in bipolar illness. Psychiatr Genet 22:253-255 (C) 2012 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:253 / 255
页数:3
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