Department of Biology and Physics, Kennesaw State University, 1000 Chastain Rd. Bldg 12 Rm 308, Kennesaw, GA 30144, USA.
Inflamm Res. 2011 Mar;60(3):213-7. doi: 10.1007/s00011-010-0286-1. Epub 2010 Dec 14.
This report describes a focused immediate early gene response by human umbilical vein endothelial cells (HUVEC) to Echis carinatus snake venom.
Primary cultures of HUVEC were used to assess acute inflammatory gene responses.
Crude E. carinatus venom (2.5 µg/ml) was used to stimulate HUVEC.
HUVEC stimulated for 3 h with E. carinatus venom showed a focused response to the venom, with significant increases in metallothionein (e.g., MT1H, MT2A, MT1X) and cytochrome P450 (e.g., CYP1A1, CYP1B1) gene expressions compared to non-stimulated controls. Several other genes involved in cell growth and matrix attachment were repressed [e.g., thrombospondin 1 (THBS1), connective tissue growth factor (CTGF)].
These data suggest that acute vascular injury induced by hemorrhagic snake venom initiates an anti-oxidant response primarily involving metallothioneins.
本报告描述了人脐静脉内皮细胞(HUVEC)对 Echis carinatus 蛇毒的特定即刻早期基因反应。
使用原代培养的 HUVEC 来评估急性炎症基因反应。
使用粗制的 E. carinatus 蛇毒液(2.5µg/ml)刺激 HUVEC。
与未刺激对照相比,用 E. carinatus 蛇毒刺激 3 小时的 HUVEC 对蛇毒表现出特定的反应,金属硫蛋白(例如 MT1H、MT2A、MT1X)和细胞色素 P450(例如 CYP1A1、CYP1B1)基因表达显著增加。其他几个参与细胞生长和基质附着的基因受到抑制[例如,血小板反应蛋白 1(THBS1)、结缔组织生长因子(CTGF)]。
这些数据表明,出血性蛇毒引起的急性血管损伤会引发主要涉及金属硫蛋白的抗氧化反应。