Chen G, Gao W, Li Y, Kang L, Li Y, Meng Z, Ma D, Tang J
Institute of Cardiovascular Research, Beijing Medical University, Beijing 100083, China.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2000 Aug;22(4):383-7.
To investigate the mechanisms resulting in cardiovascular diseases and birth defect.
Induced screening and differential display, Northern blot, and immunohistochemistry assay were applied to clone the homocysteine-induced gene HCY-2 and detect the expression of HCY-2 gene respectively.
A novel HCY-induced full length cDNA--HCY-2 which encodes 142 amino acids was obtained from vascular smooth muscle cells of rats. Results of the Northern blot and immunohistochemistry assays suggest that it widely expresses in many kinds of tissues such as heart, kidney, brain, liver, and lung. In vitro, we transferred recombinant HCY-2 gene into endothelial cells and found that it could induce apoptosis and DNA injury. In vivo, HCY-2 gene could induce chicken embryo cells apoptosis and embryo malformation.
The results indicated that HCY-2 gene might be a novel apoptosis-inducing gene and might be involved in the pathogenesis of cardiovascular diseases and birth defects induced by hyperhomocysteinemia.
研究导致心血管疾病和出生缺陷的机制。
应用诱导筛选和差异显示、Northern印迹及免疫组织化学分析分别克隆同型半胱氨酸诱导基因HCY - 2并检测HCY - 2基因的表达。
从大鼠血管平滑肌细胞中获得了一个新的HCY诱导的全长cDNA——HCY - 2,其编码142个氨基酸。Northern印迹和免疫组织化学分析结果表明,它在心脏、肾脏、脑、肝脏和肺等多种组织中广泛表达。在体外,我们将重组HCY - 2基因转入内皮细胞,发现它可诱导细胞凋亡和DNA损伤。在体内,HCY - 2基因可诱导鸡胚细胞凋亡和胚胎畸形。
结果表明,HCY - 2基因可能是一个新的凋亡诱导基因,可能参与高同型半胱氨酸血症诱导的心血管疾病和出生缺陷的发病机制。