Sasaki Tsutomu, Kitagawa Kazuo, Sugiura Shiro, Omura-Matsuoka Emi, Tanaka Shigeru, Yagita Yoshiki, Okano Hideyuki, Matsumoto Masayasu, Hori Masatsugu
Division of Strokology, Department of Internal Medicine and Therapeutics, Osaka University Graduate School of Medicine, Osaka, Japan.
J Neurosci Res. 2003 May 15;72(4):461-71. doi: 10.1002/jnr.10595.
Global ischemia promotes neurogenesis in the dentate gyrus of the adult mouse hippocampus. Cyclooxygenase (COX)-2, the principal isoenzyme in the brain, modulates inflammation, glutamate-mediated cytotoxicity, and synaptic plasticity. We demonstrated that delayed treatment with different classes of COX inhibitor significantly blunted enhancement of dentate gyrus proliferation of neural progenitor cells after ischemia. COX-2 immunoreactivity was observed in both neurons and astrocytes in the dentate gyrus, but not in neural progenitor cells in the subgranular zone. Moreover, in the postischemic dentate gyrus of heterozygous and homozygous COX-2 knockout mice, proliferating bromodeoxyuridine-positive cells were significantly fewer than in wild-type littermates. These results demonstrate that COX-2 is an important modulator in enhancement of proliferation of neural progenitor cells after ischemia.
全脑缺血促进成年小鼠海马齿状回的神经发生。环氧化酶(COX)-2是脑中主要的同工酶,可调节炎症、谷氨酸介导的细胞毒性和突触可塑性。我们证明,用不同种类的COX抑制剂进行延迟治疗可显著减弱缺血后齿状回神经祖细胞增殖的增强。在齿状回的神经元和星形胶质细胞中均观察到COX-2免疫反应性,但在颗粒下区的神经祖细胞中未观察到。此外,在杂合子和纯合子COX-2基因敲除小鼠的缺血后齿状回中,增殖的溴脱氧尿苷阳性细胞明显少于野生型同窝小鼠。这些结果表明,COX-2是缺血后神经祖细胞增殖增强的重要调节因子。