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Journal: Journal of Neuroinflammation
Article Title: Clemastine improves hypomyelination in rats with hypoxic–ischemic brain injury by reducing microglia-derived IL-1β via P38 signaling pathway
doi: 10.1186/s12974-019-1662-6
Figure Lengend Snippet: Clemastine improves axonal hypomyelination via inhibition of p38 phosphorylation in microglial cells. Panel a showing phosphorylation-p38 (38 kDa) and total-p38 (38 kDa) immunoreactive bands. Panel b is bar graph which indicates that expression of p-p38 were improved in the AMCs after OGD administration for 1 h. The clemastine and MCC950 may attenuate the increment. Panel c showing IL-1β (17 kDa), NLRP3 (62 kDa), and β-actin (42 kDa) immunoreactive bands. Panels d and e are bar graphs showing the expression of IL-1β and NLRP3 were significantly up-regulated at 1 h after treatment with OGD compared with the controls. Clemastine could reduce the high expressions of NLRP3 and IL-1β proteins by inhibiting the p-p38. The inhibition was strengthened after adding additional MCC950 or SB203580 (a specific p38 pathway inhibitor). Panel f showing MBP (32 kDa), CNPase (48 kDa), and β-actin (42 kDa) immunoreactive bands. Panels h and g are bar graphs showing the protein expressions of MBP and CNPase were significantly downregulated at 7 days after OGD compared with the controls. Clemastine and SB203580 could upregulate the expressions of MBP and CNPase proteins induced by OGD by inhibiting the p-p38. When additional MCC950 or SB203580 was added, the expression of MBP was upregulated compared with the OGD + clemastine group. N =3. * P < 0.05
Article Snippet: To study the effect of clemastine on the p38 signaling pathways under hypoxic condition, microglial cells were divided into six groups: Control group, OGD group, OGD + 20ng/ml clemastine group, OGD + 20ng/ml clemastine + 0.1μM MCC950 group, OGD + 20ng/ml clemastine + 0.5μM
Techniques: Inhibition, Phospho-proteomics, Expressing