| Literature DB >> 33782126 |
Si-Yao Lu1, Chong-Lei Fu1, Liang Liang2,3,4, Bo Yang1, Wei Shen1, Qiu-Wen Wang1, Yun Chen1, Yan-Fen Chen1, Yao-Nan Liu1, Lin Zhu1, Jieqing Zhao1, Wei Shi4, Shuangli Mi2,3,4, Jun Yao5.
Abstract
microRNA-218 (miR-218) has been linked to several cognition related neurodegenerative and neuropsychiatric disorders. However, whether miR-218 plays a direct role in cognitive functions remains unknown. Here, using the miR-218 knockout (KO) mouse model and the sponge/overexpression approaches, we showed that miR-218-2 but not miR-218-1 could bidirectionally regulate the contextual and spatial memory in the mice. Furthermore, miR-218-2 deficiency induced deficits in the morphology and presynaptic neurotransmitter release in the hippocampus to impair the long term potentiation. Combining the RNA sequencing analysis and luciferase reporter assay, we identified complement component 3 (C3) as a main target gene of miR-218 in the hippocampus to regulate the presynaptic functions. Finally, we showed that restoring the C3 activity in the miR-218-2 KO mice could rescue the synaptic and learning deficits. Therefore, miR-218-2 played an important role in the cognitive functions of mice through C3, which can be a mechanism for the defective cognition of miR-218 related neuronal disorders.Entities:
Keywords: C3; LTP; hippocampus; miR-218; synapse
Year: 2021 PMID: 33782126 PMCID: PMC8040660 DOI: 10.1073/pnas.2021770118
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205