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短暂性脑缺血仅在沙鼠海马体CA1区的小胶质细胞中诱导白蛋白表达。

Transient cerebral ischemia induces albumin expression in microglia only in the CA1 region of the gerbil hippocampus.

作者信息

Park Joon Ha, Park Jin-A, Ahn Ji Hyeon, Kim Yang Hee, Kang Il Jun, Won Moo-Ho, Lee Choong-Hyun

机构信息

Department of Biomedical Science, Research Institute of Bioscience and Biotechnology, Chuncheon, Gangwon 24252, Republic of Korea.

Department of Pharmacy, College of Pharmacy, Dankook University, Cheonan, South Chungcheong 31116, Republic of Korea.

出版信息

Mol Med Rep. 2017 Jul;16(1):661-665. doi: 10.3892/mmr.2017.6671. Epub 2017 May 31.

Abstract

Albumin, the most abundant plasma protein, is known to exhibit a neuroprotective effect in animal models of focal and global cerebral ischemia. In the present study, the expression and immunoreactivity of albumin was examined in the hippocampus following 5 min of transient cerebral ischemia in gerbils. Albumin immunoreactivity was observed in microglia of the CA1 hippocampal region 2 days post‑ischemic insult, and it was significantly increased at 4 days following ischemia-reperfusion. In addition, at 4 days post‑ischemic insult, albumin‑immunoreactive microglia were abundant in the stratum pyramidale of the CA1 region. The present results demonstrated that albumin was newly expressed post‑injury in microglia in the CA1 region, suggesting ischemia‑induced neuronal loss. Albumin expression may therefore be associated with ischemia‑induced delayed neuronal death in the CA1 region following transient cerebral ischemia.

摘要

白蛋白是血浆中含量最丰富的蛋白质,已知其在局灶性和全脑缺血的动物模型中具有神经保护作用。在本研究中,检测了沙土鼠短暂性脑缺血5分钟后海马中白蛋白的表达及免疫反应性。缺血性损伤2天后,在海马CA1区的小胶质细胞中观察到白蛋白免疫反应性,且在缺血再灌注4天后显著增加。此外,在缺血性损伤4天时,CA1区锥体层中富含白蛋白免疫反应性小胶质细胞。本研究结果表明,损伤后白蛋白在CA1区的小胶质细胞中重新表达,提示缺血诱导的神经元丢失。因此,白蛋白表达可能与短暂性脑缺血后CA1区缺血诱导的迟发性神经元死亡有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4c7/5482121/e21c2c9a66ad/MMR-16-01-0661-g00.jpg

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