Stephens T W, Basinski M, Bristow P K, Bue-Valleskey J M, Burgett S G, Craft L, Hale J, Hoffmann J, Hsiung H M, Kriauciunas A
Technology Core Division, Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana 46285, USA.
Nature. 1995 Oct 12;377(6549):530-2. doi: 10.1038/377530a0.
Recently Zhang et al. cloned a gene that is expressed only in adipose tissue of the mouse. The obese phenotype of the ob/ob mouse is linked to a mutation in the obese gene that results in expression of a truncated inactive protein. Human and rat homologues for this gene are known. Previous experiments predict such a hormone to have a hypothalamic target. Hypothalamic neuropeptide Y stimulates food intake, decreases thermogenesis, and increases plasma insulin and corticosterone levels making it a potential target. Here we express the obese protein in Escherichia coli and find that it suppresses food intake and decreases body weight dramatically when administered to normal and ob/ob mice but not db/db (diabetic) mice, which are thought to lack the appropriate receptor. High-affinity binding was detected in the rat hypothalamus. One mechanism by which this protein regulated food intake and metabolism was inhibition of neuropeptide-Y synthesis and release.
最近,张等人克隆了一个仅在小鼠脂肪组织中表达的基因。ob/ob小鼠的肥胖表型与肥胖基因的突变有关,该突变导致截短的无活性蛋白的表达。已知该基因的人类和大鼠同源物。先前的实验预测这种激素有一个下丘脑靶点。下丘脑神经肽Y刺激食物摄入,减少产热,并增加血浆胰岛素和皮质酮水平,使其成为一个潜在的靶点。在这里,我们在大肠杆菌中表达肥胖蛋白,发现当将其施用于正常小鼠和ob/ob小鼠时,它会显著抑制食物摄入并降低体重,但对db/db(糖尿病)小鼠无效,据认为db/db小鼠缺乏合适的受体。在大鼠下丘脑中检测到高亲和力结合。这种蛋白质调节食物摄入和新陈代谢的一种机制是抑制神经肽Y的合成和释放。