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盐皮质激素和糖皮质激素受体在结肠细胞中的类固醇结合与定位

Mineralocorticoid and glucocorticoid receptor steroid binding and localization in colonic cells.

作者信息

Schulman G, Robertson N M, Elfenbein I B, Eneanya D, Litwack G, Bastl C P

机构信息

Department of Medicine, Temple University Health Sciences Center, Philadelphia 19140.

出版信息

Am J Physiol. 1994 Mar;266(3 Pt 1):C729-40. doi: 10.1152/ajpcell.1994.266.3.C729.

Abstract

In rat colon epithelium glucocorticoids and mineralocorticoids regulate Na transport by binding to distinct receptors and stimulating different pathways. The distribution and intracellular localization of mineralocorticoid (MR) and glucocorticoid (GR) receptors in colonic Na-absorbing surface cells and Cl-secreting crypt cells is unknown. Surface and crypt cells were sequentially isolated from rat distal colon by EDTA chelation and mechanical dissociation. Cell viability was confirmed by trypan blue exclusion and low rates of 2',7'-bis(2-carboxyethyl)-5(6)-carboxylfluorescein leak. Histologic examination, alkaline phosphatase activity, and rates of [3H]leucine incorporation confirmed separation of surface from crypt cells. Scatchard analysis of [3H]aldosterone and [3H]triamcinolone acetonide binding demonstrated that the number of MR decreased from 7,228 +/- 1,067 in surface to 2,299 +/- 434 receptors/cell in crypt cells, whereas the number of GR increased from 20,857 +/- 4,241 in surface to 58,598 +/- 8,207 receptors/cell in crypt cells. The dissociation constants were 2.8 +/- 0.4 nM for the MR and 12 +/- 3 nM for the GR. Indirect immunofluorescence using the specific anti-MR antibody hMRsN and the anti-GR antibody BuGR-2 demonstrated that both unliganded receptors were cytoplasmic and translocated to the nucleus after hormone binding. These data indicate that both surface and crypt cells are potentially responsive to mineralocorticoids and glucocorticoids and that both the MR and GR require hormone for nuclear translocation.

摘要

在大鼠结肠上皮细胞中,糖皮质激素和盐皮质激素通过与不同受体结合并刺激不同途径来调节钠转运。盐皮质激素(MR)和糖皮质激素(GR)受体在结肠钠吸收表面细胞和氯分泌隐窝细胞中的分布及细胞内定位尚不清楚。通过EDTA螯合和机械解离从大鼠远端结肠依次分离出表面细胞和隐窝细胞。通过台盼蓝排斥试验和低速率的2',7'-双(2-羧乙基)-5(6)-羧基荧光素泄漏来确认细胞活力。组织学检查、碱性磷酸酶活性以及[3H]亮氨酸掺入率证实了表面细胞与隐窝细胞的分离。对[3H]醛固酮和[3H]曲安奈德结合的Scatchard分析表明,MR的数量从表面细胞中的7228±1067个受体/细胞减少到隐窝细胞中的2299±434个受体/细胞,而GR的数量从表面细胞中的20857±4241个受体/细胞增加到隐窝细胞中的58598±8207个受体/细胞。MR的解离常数为2.8±0.4 nM,GR的解离常数为12±3 nM。使用特异性抗MR抗体hMRsN和抗GR抗体BuGR-2进行间接免疫荧光显示,两种未结合配体的受体均位于细胞质中,激素结合后转位至细胞核。这些数据表明,表面细胞和隐窝细胞都可能对盐皮质激素和糖皮质激素有反应,并且MR和GR都需要激素才能进行核转位。

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