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. Author manuscript; available in PMC: 2020 Jul 1.
Published in final edited form as: Neurobiol Dis. 2019 Mar 5;127:163–177. doi: 10.1016/j.nbd.2019.03.001

Figure 10. Immunocytochemical analysis of the effects of systemic delivery of the siα-syn conjugated to C2-9r or ApoB11 peptides on microgliosis in the brains of α-syn tg mice.

Figure 10.

Four-month-old α-syn tg and non-tg mice received repeated intraperitoneal injections of scrambled siRNA (si-sc) or α-syn siRNA (si-αsyn) conjugated to either C2-9r or ApoB11 and were sacrificed 4 weeks later for analysis. Sections were immunolabeled with an antibody against the microglia cell marker-Iba1. (A) Representative images of the neocortex, hippocampus and striatum of non-tg and α-syn tg mice treated with either si-sc or si-αsyn conjugated with C2-9r or ApoB11 of sections immunostained with the Iba1 antibody. Image analysis of the relative numbers of Iba1 immunoreactive cells per 102 in the (B) neocortex, (C) hippocampus (CA3), and (D) striatum. One-way ANOVA with poshoc Dunnet when comparing to control and Tukey-Kramer when comparing in between groups. * indicates statistical significance p < 0.05 compared to non-tg mice. ** p < 0.05 compared to C2-9r/si-sc. # indicates statistical significance p < 0.05 compared to α-syn-tg mice treated with ApoB11/si-sc. Scale bar represents 250 μm for low magnification panels and 25 μm for higher magnification panels. Non-tg (n=16) and α-syn tg (n=24).