|  Help  |  About  |  Contact Us

Publication : MicroRNA-7 Enhances Subventricular Zone Neurogenesis by Inhibiting NLRP3/Caspase-1 Axis in Adult Neural Stem Cells.

First Author  Fan Z Year  2016
Journal  Mol Neurobiol Volume  53
Issue  10 Pages  7057-7069
PubMed ID  26676570 Mgi Jnum  J:329750
Mgi Id  MGI:6844097 Doi  10.1007/s12035-015-9620-5
Citation  Fan Z, et al. (2016) MicroRNA-7 Enhances Subventricular Zone Neurogenesis by Inhibiting NLRP3/Caspase-1 Axis in Adult Neural Stem Cells. Mol Neurobiol 53(10):7057-7069
abstractText  alpha-Synuclein (alpha-syn) has been recognized to induce neuroinflammation and to disturb nerve repair process in Parkinson's disease. However, the potential mechanisms underlying alpha-syn-induced impairment of adult neurogenesis remain unclear. In the present study, A53T mutant alpha--synuclein transgenic (A53T(tg/tg)) mice, caspase-1 knockout mice, and A53T(tg/tg);caspase-1(-/-) double transgenic mice were used to prepare adult neural stem cells (ANSCs) and to investigate inflammasome-related mechanism for alpha-syn-impaired neurogenesis in mouse subventricular zone (SVZ). We showed that alpha-syn inhibited neurogenesis in the SVZ of A53T(tg/tg) mice and impaired proliferation and differentiation in ANSCs cultured in vitro, accompanied by reduced microRNA-7 (miR-7) expression levels. We further found that ANSC expressed NLRP3-containing inflammasome and alpha-syn activated both TLR4/NF-kappaB and NLRP3/caspase-1 signals in ANSCs. Either Nlrp3 knockdown or Caspase-1 knockout could attenuate the inhibition of proliferation in ANSCs induced by alpha-syn. Furthermore, we demonstrated that miR-7 post-transcriptionally controlled Nlrp3 expression besides targeting alpha-syn. Most notably, stereotactic injection of miR-7 mimics into lateral ventricles significantly inhibited NLRP3 inflammasome activation and improved adult neurogenesis in mouse SVZ. Our study provides a direct link between NLRP3 inflammasome activation and alpha-syn-impaired neurogenesis in the pathogenesis of alpha-synucleinopathies.
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

6 Authors

13 Bio Entities

0 Expression