Abstract
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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 253-255 |
| Number of pages | 3 |
| Journal | Psychiatric Genetics |
| Volume | 22 |
| Issue number | 5 |
| DOIs | |
| State | Published - Oct 2012 |
Keywords
- apoptosis
- bipolar disorder
- brain-derived neurotrophic factor
- intracellular sodium
- single nucleotide polymorphism
ASJC Scopus subject areas
- Genetics
- Psychiatry and Mental health
- Genetics(clinical)
- Biological Psychiatry
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