Choi K W, Bloom A D
Science. 1970 Oct 2;170(3953):89-90. doi: 10.1126/science.170.3953.89.
Two lymphocytoid cell lines have been established from a patient with the Lesch-Nyhan syndrome. The cells are deficient in hypoxanthine-guanine phosphoribosyltransferase, as demonstrated by their failure to incorporate [H(3)]hypoxanthine and by their inability to grow in medium in which they were nutritionally dependent upon exogenous hypoxanthine. This represents the first establishment of presumptively permanent human lymphocytoid cell lines that are deficient in a specific enzyme.
已从一名患有莱施-尼汉综合征的患者身上建立了两个淋巴样细胞系。这些细胞缺乏次黄嘌呤-鸟嘌呤磷酸核糖转移酶,这可通过它们不能掺入[H(3)]次黄嘌呤以及它们无法在营养上依赖外源性次黄嘌呤的培养基中生长得到证明。这代表了首次建立了推定永久性的、缺乏特定酶的人类淋巴样细胞系。