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长期低压缺氧后的内皮激活。

Endothelial activation following prolonged hypobaric hypoxia.

作者信息

Dore-Duffy P, Balabanov R, Beaumont T, Hritz M A, Harik S I, LaManna J C

机构信息

Division of Neuroimmunology, Wayne State University School of Medicine and the Detroit Medical Center, 4201 St. Antoine, 6E UHC, Detroit, Michigan, 48201, USA.

出版信息

Microvasc Res. 1999 Mar;57(2):75-85. doi: 10.1006/mvre.1998.2112.

Abstract

Prolonged exposure to low oxygen may induce adaptive changes which can be either beneficial or deleterious to cell survival. We examined the effect of prolonged moderate hypobaric hypoxia on CNS endothelial cell (EC) function. Exposure to hypoxia resulted in expression of EC activation markers, the cell surface adhesion proteins intracellular adhesion molecule-1 and E-selectin. Induction of the major histocompatibility complex (MHC) class II molecule as well as increased constitutive expression of the transferrin receptor and the glucose transporter-1 protein was also detected within 24 h of exposure to hypobaric hypoxia. Constitutive expression of the MHC class I molecule increased by 48 h. Expression of most EC activation markers increased with time from 0 to 2 weeks. By 3 weeks of exposure to hypobaric hypoxia, ECs returned to their quiescent state with the exception of sustained expression of E-selectin and elevated glut-1. Little to no significant increase in expression of vascular cell adhesion molecule-1 was seen at any time period.

摘要

长期暴露于低氧环境可能会引发适应性变化,这些变化对细胞存活可能有益,也可能有害。我们研究了长期中度低压缺氧对中枢神经系统内皮细胞(EC)功能的影响。暴露于缺氧环境会导致EC活化标志物、细胞表面粘附蛋白细胞间粘附分子-1和E-选择素的表达。在暴露于低压缺氧环境的24小时内,还检测到主要组织相容性复合体(MHC)II类分子的诱导以及转铁蛋白受体和葡萄糖转运蛋白-1蛋白的组成性表达增加。MHC I类分子的组成性表达在48小时时增加。大多数EC活化标志物的表达在0至2周内随时间增加。到暴露于低压缺氧环境3周时,除了E-选择素的持续表达和glut-1升高外,EC恢复到静止状态。在任何时间段内,血管细胞粘附分子-1的表达几乎没有明显增加。

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