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哺乳动物和鸟类肝细胞核中的一种1,25 - 二羟基维生素D3受体样蛋白。

A 1,25-dihydroxyvitamin D3 receptor-like protein in mammalian and avian liver nuclei.

作者信息

Duncan W E, Whitehead D, Wray H L

机构信息

Department of Medicine, Walter Reed Army Medical Center, Washington, D.C. 20307-5001.

出版信息

Endocrinology. 1988 Jun;122(6):2584-9. doi: 10.1210/endo-122-6-2584.

Abstract

The actions of 1,25-dihydroxyvitamin D3 [1,25-(OH)2D3] are thought to be mediated through receptor proteins which have been described in a variety of avian and mammalian tissues, but not in the liver. To determine if a binding protein for 1,25-(OH)2D3 is present in this tissue, rat liver was homogenized in a low ionic strength buffer containing 10 mM Tris (pH 7.4), 2.2 m sucrose, 3 mM calcium chloride, 0.2% Triton X-100, and 0.04% Trasylol (sucrose buffer) and centrifuged over a 10-ml cushion of sucrose buffer at 61,000 x g for 80 min at 4 C. The resultant nuclear pellet was extracted in a 26 mM Tris (pH 7.4) buffer containing 0.3 M potassium chloride, 5 mM dithiothreitol, 1 mM EDTA, and 10 mM sodium molybdate. Saturable 1,25-(OH)2D3 binding was identified in high salt extracts of rat liver nuclei and was eliminated by treatment with trypsin. This liver binding protein cosediments on high salt 5-20% sucrose density gradients with the 1,25-(OH)2D3 receptor protein from intestine and is distinct from the 6.OS tissue binding protein for 25-hydroxyvitamin D3. Perfusion of rat liver with PBS to remove receptor-positive blood cells before isolation of the nuclei did not change 1,25-(OH)2D3 binding. The nuclear protein bound 1,25-(OH)2D3 more avidly than either 24,25-(OH)2 D3 or 25-hydroxyvitamin D3. Saturation analysis of 1,25-(OH)2D3 binding revealed an apparent equilibrium dissociation constant of 20.6 +/- 2.2 pM (mean +/- SEM) at 4 C and a maximum binding capacity of 49.0 +/- 14.6 fmol/extract from 1.0 mg DNA. The 1,25-(OH)2D3-binding binding protein was present in liver nuclei isolated from mice, rabbits, and chicks and in nuclei isolated from cultured rat hepatocytes. The ligand specificity, sedimentation coefficient, limited binding capacity, trypsin sensitivity, and nuclear location of the hepatic 1,25-(OH)2D3-binding protein are similar to those of 1,25-(OH)2D3 receptors described in other tissues and suggest that the liver may be a target organ for [1,25-(OH)2D3] action.

摘要

1,25 - 二羟基维生素D3[1,25 - (OH)2D3]的作用被认为是通过受体蛋白介导的,这种受体蛋白已在多种禽类和哺乳动物组织中被描述,但在肝脏中尚未发现。为了确定该组织中是否存在1,25 - (OH)2D3结合蛋白,将大鼠肝脏在含有10 mM Tris(pH 7.4)、2.2 m蔗糖、3 mM氯化钙、0.2% Triton X - 100和0.04%抑肽酶(蔗糖缓冲液)的低离子强度缓冲液中匀浆,并在4℃下以61,000×g在10 ml蔗糖缓冲液垫层上离心80分钟。所得核沉淀用含有0.3 M氯化钾、5 mM二硫苏糖醇、1 mM EDTA和10 mM钼酸钠的26 mM Tris(pH 7.4)缓冲液提取。在大鼠肝细胞核的高盐提取物中鉴定出可饱和的1,25 - (OH)2D3结合,并且通过胰蛋白酶处理可消除这种结合。这种肝脏结合蛋白在高盐5 - 20%蔗糖密度梯度上与来自肠道的1,25 - (OH)2D3受体蛋白共沉降,并且与25 - 羟基维生素D3的6.0S组织结合蛋白不同。在分离细胞核之前用PBS灌注大鼠肝脏以去除受体阳性血细胞,这并不改变1,25 - (OH)2D3结合。该核蛋白与1,25 - (OH)2D3的结合比与24,25 - (OH)2D3或25 - 羟基维生素D3的结合更紧密。对1,25 - (OH)2D3结合的饱和分析显示,在4℃下表观平衡解离常数为20.6±2.2 pM(平均值±标准误),最大结合容量为49.0±14.6 fmol/从1.0 mg DNA提取的提取物。1,25 - (OH)2D3结合蛋白存在于从小鼠、兔子和小鸡分离的肝细胞核以及从培养的大鼠肝细胞分离的细胞核中。肝脏1,25 - (OH)2D3结合蛋白的配体特异性、沉降系数、有限的结合容量、胰蛋白酶敏感性和核定位与其他组织中描述的1,25 - (OH)2D3受体相似,这表明肝脏可能是[1,25 - (OH)2D3]作用的靶器官。

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