PMID- 24115234 OWN - NLM STAT- MEDLINE DCOM- 20140818 LR - 20131211 IS - 1098-1063 (Electronic) IS - 1050-9631 (Linking) VI - 24 IP - 1 DP - 2014 Jan TI - Transcriptome profiling analysis of the mechanisms underlying the BDNF Val66Met polymorphism induced dysfunctions of the central nervous system. PG - 65-78 LID - 10.1002/hipo.22204 [doi] AB - Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism affects postnatal behaviors and is associated with a variety of neuropsychiatric disorders. However, the mechanisms underlying the BDNF(Met) variant induced dysfunctions of the central nervous system remain obscure. In order to identify the candidate genes and pathways responsible for the dysfunctions associated with this BDNF variation, we analyzed the expression of genes in the hippocampus, prefrontal cortex, and amygdala of the BDNF(Met) variant mice in comparison with the wild-type mice using Illumina bead microarray. Transcriptome profiling analysis revealed region-distinctive and gene-dose dependent changes of gene expression associated with the BDNF(Met) variant. BDNF(Met) variant mice exhibited altered expression of genes associated with translational machinery, neuronal plasticity and mitochondrial function based on the gene ontology (GO) annotation. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis revealed that the chemokine, cell adhesion, ubiquitin-proteosome and wnt signaling pathways were altered in the BDNF(Met) variant mice brain. Finally, the CX3CL1/CX3CR1 signaling was identified to be impaired in the hippocampus and microinjection of CX3CL1 into the hippocampus could rescue the hippocampal dependent memory deficits in BDNF(Met/Met) mice, indicating that CX3CL1 may be an effective treatment option for memory disorders in humans with this genetic BDNF variation. These findings will help us further understanding the molecular mechanisms involved in the BDNF(Met) associated behavior and neuroanatomy alternations. CI - Copyright (c) 2013 Wiley Periodicals, Inc. FAU - Wang, Dong-Dong AU - Wang DD AD - Department of Neurobiology, Shandong Provincial Key Laboratory of Mental Disorders, School of Medicine, Shandong University, Jinan, Shandong, 250012, People's Republic of China. FAU - Tian, Tian AU - Tian T FAU - Dong, Qing AU - Dong Q FAU - Xu, Xu-Feng AU - Xu XF FAU - Yu, Hui AU - Yu H FAU - Wang, Yue AU - Wang Y FAU - Chen, Zhe-Yu AU - Chen ZY LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20131015 PL - United States TA - Hippocampus JT - Hippocampus JID - 9108167 RN - 0 (Brain-Derived Neurotrophic Factor) SB - IM MH - Animals MH - Blotting, Western MH - Brain/*physiology MH - Brain-Derived Neurotrophic Factor/*genetics MH - Immunohistochemistry MH - Mental Disorders/*genetics MH - Mice MH - Oligonucleotide Array Sequence Analysis MH - Polymorphism, Single Nucleotide/*genetics MH - Real-Time Polymerase Chain Reaction MH - Reverse Transcriptase Polymerase Chain Reaction MH - *Transcriptome OTO - NOTNLM OT - BDNF Val66Met OT - CX3CL1/CX3CR1 OT - hippocampus OT - memory OT - microarray EDAT- 2013/10/12 06:00 MHDA- 2014/08/19 06:00 CRDT- 2013/10/12 06:00 PHST- 2013/08/26 00:00 [accepted] PHST- 2013/10/12 06:00 [entrez] PHST- 2013/10/12 06:00 [pubmed] PHST- 2014/08/19 06:00 [medline] AID - 10.1002/hipo.22204 [doi] PST - ppublish SO - Hippocampus. 2014 Jan;24(1):65-78. doi: 10.1002/hipo.22204. Epub 2013 Oct 15.