Le Blanc P E, Roncari D A, Hoar D I, Adachi A M
Department of Medicine, University of Calgary, Alberta, Canada.
J Clin Invest. 1988 May;81(5):1639-45. doi: 10.1172/JCI113499.
To learn about adipose differentiation of precursors from postnatal adipose tissue of lean and massively obese subjects, human omental adipocyte precursor-murine renal adenocarcinoma cell (RAG) hybrids were formed by fusion with polyethylene glycol, and cultured selectively with 50 microM ouabain in hypoxanthine aminopterin thymidine (HAT) medium. Under conditions in which the parent cells did not differentiate, a number of hybrids, which were cloned, revealed morphologic and biochemical evidence of differentiation. In addition to activation of human genes within the common nucleus of the hybrids, murine cytoplasmic activators are probably also involved because heterocaryons (fused cells with two interspecific nuclei) revealed the same phenomenon. Hybrids composed of precursors from massively obese subjects disclosed more frequent and prominent differentiation. Since these hybrids, in contrast to those from the lean, recapitulate this phenomenon in subcultures, they provide the potential system for mapping the human gene(s) responsible for adipose differentiation and its exaggeration in massive obesity.
为了了解瘦人和极度肥胖者出生后脂肪组织中前体细胞的脂肪分化情况,通过聚乙二醇融合法构建了人网膜脂肪细胞前体-小鼠肾腺癌细胞(RAG)杂交细胞,并在次黄嘌呤氨基蝶呤胸腺嘧啶核苷(HAT)培养基中用50微摩尔哇巴因进行选择性培养。在亲本细胞未分化的条件下,许多克隆的杂交细胞显示出分化的形态学和生化证据。除了杂交细胞共同细胞核内人类基因的激活外,小鼠细胞质激活剂可能也参与其中,因为异核体(具有两个种间细胞核的融合细胞)也显示出相同的现象。由极度肥胖者的前体细胞组成的杂交细胞表现出更频繁和显著的分化。由于这些杂交细胞与瘦人来源的杂交细胞不同,在传代培养中重现了这一现象,它们为定位负责脂肪分化及其在极度肥胖中过度表现的人类基因提供了潜在的系统。