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小鼠P1798淋巴肉瘤中糖皮质激素受体的类固醇结合和非类固醇结合形式的鉴定与定位

Identification and localization of steroid-binding and nonsteroid-binding forms of the glucocorticoid receptor in the mouse P1798 lymphosarcoma.

作者信息

Rowan B G, Ip M M

机构信息

Department of Experimental Therapeutics, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.

出版信息

J Steroid Biochem Mol Biol. 1995 May;52(5):437-50. doi: 10.1016/0960-0760(94)00193-p.

Abstract

Glucocorticoid receptors (GCRs) were characterized in sublines of the mouse P1798 lymphosarcoma that are sensitive (S) or resistant (R) to glucocorticoid-mediated apoptosis. Previous work had identified two steroid-binding GCRs in S and R cells: a 97 kDa wild-type GCR in S cells (WT-GCR), and a 45 kDa truncated GCR in R cells (TR-GCR). A third GCR, a 97 kDa nonsteroid-binding GCR (NSB-GCR), was also identified in R cells. Using subcellular fractionation and Western blotting, we now show that in contrast to the WT-GCR which is localized in both the cytoplasm and nucleus of S cells, the NSB-GCR is localized predominantly in R cell nuclei. Moreover, gel filtration chromatography revealed that treatment with 400 mM NaCl and heat did not significantly alter the Stokes radius of the NSB-GCR suggesting that this receptor is not present in a heterooligomeric complex with other proteins. The TR-GCR was localized predominantly in the soluble cytoplasmic fraction but also in the crude membrane fractions of R cell nuclei, suggesting that this receptor is tightly associated with nuclear structures. It was not detected in the soluble nuclear fraction. Unexpectedly, a 45 kDa nonsteroid-binding immunoreactive protein was detected in crude membrane fractions of S cells. These studies describe a complex GCR system in the P1798 lymphosarcoma that necessitates a further consideration of glucocorticoid signaling in S and R cells.

摘要

在对糖皮质激素介导的凋亡敏感(S)或耐药(R)的小鼠P1798淋巴肉瘤亚系中对糖皮质激素受体(GCRs)进行了表征。先前的研究已经在S和R细胞中鉴定出两种类固醇结合GCR:S细胞中的97 kDa野生型GCR(WT-GCR),以及R细胞中的45 kDa截短型GCR(TR-GCR)。在R细胞中还鉴定出了第三种GCR,即97 kDa非类固醇结合GCR(NSB-GCR)。使用亚细胞分级分离和蛋白质印迹法,我们现在表明,与定位于S细胞细胞质和细胞核中的WT-GCR不同,NSB-GCR主要定位于R细胞核中。此外,凝胶过滤色谱显示,用400 mM NaCl处理和加热并没有显著改变NSB-GCR的斯托克斯半径,这表明该受体不存在于与其他蛋白质形成的异源寡聚复合物中。TR-GCR主要定位于可溶性细胞质组分中,但也存在于R细胞核粗膜组分中,这表明该受体与核结构紧密相关。在可溶性核组分中未检测到它。出乎意料的是,在S细胞的粗膜组分中检测到了一种45 kDa非类固醇结合免疫反应蛋白。这些研究描述了P1798淋巴肉瘤中一个复杂的GCR系统,这需要进一步考虑S和R细胞中的糖皮质激素信号传导。

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