期刊
FRONTIERS IN MOLECULAR NEUROSCIENCE
卷 11, 期 -, 页码 -出版社
FRONTIERS MEDIA SA
DOI: 10.3389/fnmol.2018.00325
关键词
BDNF detection; Bdnf exon-IV and -VI; transgenic BDNF reporter mice; activity-dependent BDNF expression; long-lasting plasticity changes
资金
- Deutsche Forschungs gemeinschaft [DFG-Kni-316-10-1, FOR 2060, RU 713/3-2, SPP 1608 RU 316/12-1, KN 316/12-1]
- Brain and Behavior Research Foundation NARSAD Young Investigator Grant [20748, BFU2013-40944, DFG-STR 619/5-1, CIN-EXC 307, DFG KFO134, PRIN2010-11 2010N8PBAA, Pest-C/SAU/LA0001/2013-2014, CENTRO-01-0145-FEDER-000008, POCI-01-0145-FEDER-007440, POCI-01-0145-FEDER-028656, UID/NEU/04539/2013, UID/BIM/4501/2013]
- Open Access Publishing Fund of University of Tubingen
Bdnf exon-IV and exon-VI transcripts are driven by neuronal activity and are involved in pathologies related to sleep, fear or memory disorders. However, how their differential transcription translates activity changes into long-lasting network changes is elusive. Aiming to trace specifically the network controlled by exon-IV and -VI derived BDNF during activity-dependent plasticity changes, we generated a transgenic reporter mouse for BDNF-live-exon-visualization (BLEV), in which expression of Bdnf exon-IV and -VI can be visualized by co-expression of CFP and YFP. CFP and YFP expression was differentially activated and targeted in cell lines, primary cultures and BLEV reporter mice without interfering with BDNF protein synthesis. CFP and YFP expression, moreover, overlapped with BDNF protein expression in defined hippocampal neuronal, glial and vascular locations in vivo. So far, activity-dependent BDNF cannot be explicitly monitored independent of basal BDNF levels. The BLEV reporter mouse therefore provides a new model, which can be used to test whether stimulus-induced activity-dependent changes in BDNF expression are instrumental for long-lasting plasticity modifications.
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