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DJ-1 inhibits microglial activation and protects dopaminergic neurons in vitro and in vivo through interacting with microglial p65

机译:DJ-1抑制微胶质激活通过与微胶囊P65相互作用在体外和体内保护多巴胺能神经元

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摘要

A–C DJ-1−/− and the littermate wild-type controls were microinfused with PBS or LPS into the SN, and 14 days after injection, immunohistochemical staining was conducted. A Slices were stained with anti-IBA1 antibodies. Scale bar, 200 µm. The fluorescence intensity of IBA1 staining was quantified. n = 4. B Slices were co-stained with anti-CD14 and anti-IBA1 antibodies. Scale bar, 20 µm. The fluorescence intensity of CD14 staining was quantified. n = 4. C Slices were stained with anti-TH antibodies. Scale bar, 200 µm. TH-positive neuron numbers in the SN of each slice were quantified. n = 4.
机译:A-C. DJ-1 - / - 和凋落物野生型对照用PBS或LPS微量熔点,进入SN,注射后14天,进行免疫组化染色。用抗IBA1抗体染色切片。秤条,200μm。量化IBA1染色的荧光强度。 N = 4.b切片与抗CD14和抗IBA1抗体共染成。秤杆,20μm。量化CD14染色的荧光强度。 n = 4. C切片用抗体抗体染色。秤条,200μm。量化每片SN的Th阳性神经元数。 n = 4。

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