Title : MicroRNA-195 prevents hippocampal microglial/macrophage polarization towards the M1 phenotype induced by chronic brain hypoperfusion through regulating CX3CL1/CX3CR1 signaling.

Pub. Date : 2020 Aug 20

PMID : 32819407






6 Functional Relationships(s)
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1 RESULTS: CBH induced by 2VO initiated microglial/macrophage activation in the rat hippocampus from 1 week to 8 weeks, as evaluated by increased ratio of (CD68+ and CD206+)/Iba-1 immunofluorescence. S-(D-CARBOXYBUTYL)-L-HOMOCYSTEINE Cd68 molecule Rattus norvegicus
2 RESULTS: CBH induced by 2VO initiated microglial/macrophage activation in the rat hippocampus from 1 week to 8 weeks, as evaluated by increased ratio of (CD68+ and CD206+)/Iba-1 immunofluorescence. S-(D-CARBOXYBUTYL)-L-HOMOCYSTEINE allograft inflammatory factor 1 Rattus norvegicus
3 CONCLUSIONS: Our findings conclude that downregulation of miR-195 in the hippocampus is involved in CBH-induced microglial/macrophage polarization towards M1 phenotype by governing communication between neurons and microglia through the regulation of CX3CL1 and CX3CR1 signaling. S-(D-CARBOXYBUTYL)-L-HOMOCYSTEINE microRNA 195a Mus musculus
4 CONCLUSIONS: Our findings conclude that downregulation of miR-195 in the hippocampus is involved in CBH-induced microglial/macrophage polarization towards M1 phenotype by governing communication between neurons and microglia through the regulation of CX3CL1 and CX3CR1 signaling. S-(D-CARBOXYBUTYL)-L-HOMOCYSTEINE chemokine (C-X3-C motif) ligand 1 Mus musculus
5 CONCLUSIONS: Our findings conclude that downregulation of miR-195 in the hippocampus is involved in CBH-induced microglial/macrophage polarization towards M1 phenotype by governing communication between neurons and microglia through the regulation of CX3CL1 and CX3CR1 signaling. S-(D-CARBOXYBUTYL)-L-HOMOCYSTEINE chemokine (C-X3-C motif) receptor 1 Mus musculus
6 This indicates that miR-195 may provide a new strategy for clinical prevention and treatment of CBH. S-(D-CARBOXYBUTYL)-L-HOMOCYSTEINE microRNA 195a Mus musculus