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短暂性全脑缺血后海马CA2区半乳糖凝集素-3的表达及其受低温或抗凋亡药物的抑制作用

Galectin-3 expression in hippocampal CA2 following transient forebrain ischemia and its inhibition by hypothermia or antiapoptotic agents.

作者信息

Hisamatsu Kenji, Niwa Masayuki, Kobayashi Kazuhiro, Miyazaki Tatsuhiko, Hirata Akihiro, Hatano Yuichiro, Tomita Hiroyuki, Hara Akira

机构信息

aDepartment of Tumor Pathology, Gifu University Graduate School of Medicine bMedical Science Division, United Graduate School of Drug Discovery and Medical Information Sciences cDivision of Clinical Pathology, Gifu University Hospital dDivision of Animal Experiment, Life Science Research Center, Gifu University, Gifu, Japan.

出版信息

Neuroreport. 2016 Mar 23;27(5):311-7. doi: 10.1097/WNR.0000000000000538.

Abstract

Recent evidence has suggested that the hippocampal CA2 region plays an important role in the recognition process. We have reported that ischemic damage in the hippocampal CA2 region following transient ischemia is caused by apoptosis, but the underlying mechanisms are still not clear. Galectin-3 is a β-galactosidase-binding lectin that is important in cell proliferation and apoptotic regulation. We have also reported that galectin-3 was expressed in activated microglia in the CA1 region 96 h after transient ischemia. The aim of this study is to determine the localization and time course of galectin-3 expression in the CA2 region following transient forebrain ischemia. Galectin-3 immunostaining was observed in both interior side of CA1 region and CA2 region in hippocampus 60 h after ischemic insult. At 66 h, galectin-3 was observed in the whole CA1 region adjacent to the CA2 region in the hippocampus. Both galectin-3 expression and neuronal cell death in the CA2 region were significantly inhibited by hypothermia and by apoptosis-inhibiting reagents. These results suggest that galectin-3 in the CA2 region is expressed independent of that in the CA1 region. Protection of the expression of galectin-3 in the CA2 region might contribute toward the survival of CA2 pyramidal neurons.

摘要

近期证据表明,海马体CA2区在识别过程中发挥着重要作用。我们曾报道,短暂性缺血后海马体CA2区的缺血性损伤是由凋亡引起的,但其潜在机制仍不清楚。半乳糖凝集素-3是一种与β-半乳糖苷酶结合的凝集素,在细胞增殖和凋亡调控中起重要作用。我们还报道过,短暂性缺血96小时后,半乳糖凝集素-3在CA1区活化的小胶质细胞中表达。本研究的目的是确定短暂性前脑缺血后CA2区半乳糖凝集素-3表达的定位和时间进程。缺血损伤60小时后,在海马体CA1区内侧和CA2区均观察到半乳糖凝集素-3免疫染色。66小时时,在海马体中与CA2区相邻的整个CA1区观察到半乳糖凝集素-3。低温和凋亡抑制试剂均显著抑制了CA2区的半乳糖凝集素-3表达和神经元细胞死亡。这些结果表明,CA2区的半乳糖凝集素-3表达独立于CA1区。保护CA2区半乳糖凝集素-3的表达可能有助于CA2锥体神经元的存活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9171/4782821/5c22af976f44/wnr-27-311-g001.jpg

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