Lu Y, Pelling J C, Chaney W G
Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha 68198-4525.
Clin Exp Metastasis. 1994 Jan;12(1):47-54. doi: 10.1007/BF01784333.
NIH3T3 cells transfected with an activated Ha-ras oncogene were treated with L-PHA, the leukoagglutinin from red kidney beans. Cell lines resistant to L-PHA-mediated cytotoxicity were isolated and found to contain reduced levels of L-PHA-binding oligosaccharides. The levels of N-acetylglucosaminyltransferase V, the enzyme responsible for the initiation of the beta 1-6 branch, were reduced in L-PHA-resistant cells. Tumorigenicity in nude mice was unchanged by the change in oligosaccharide expression, but the ability to form lung tumors after intravenous injection was significantly reduced. These results demonstrate that the ability of NIH3T3 cells transfected with an activated Ha-ras oncogene to form lung tumors after intravenous injection into nude mice is reduced in all six L-PHA selected cell lines containing a reduction in beta 1-6 branched Asn-linked oligosaccharides.
用活化的Ha-ras癌基因转染的NIH3T3细胞用菜豆白细胞凝集素L-PHA处理。分离出对L-PHA介导的细胞毒性具有抗性的细胞系,发现其L-PHA结合寡糖水平降低。负责β1-6分支起始的N-乙酰葡糖胺转移酶V水平在L-PHA抗性细胞中降低。寡糖表达的变化未改变裸鼠中的致瘤性,但静脉注射后形成肺肿瘤的能力显著降低。这些结果表明,在所有六个β1-6分支的天冬酰胺连接寡糖减少的L-PHA选择的细胞系中,用活化的Ha-ras癌基因转染的NIH3T3细胞静脉注射到裸鼠后形成肺肿瘤的能力降低。