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截短型心房利钠肽受体-A的功能结构域与表达:羧基末端区域指导受体在COS-7细胞中的内化与隔离

Functional domains and expression of truncated atrial natriuretic peptide receptor-A: the carboxyl-terminal regions direct the receptor internalization and sequestration in COS-7 cells.

作者信息

Pandey K N, Kumar R, Li M, Nguyen H

机构信息

Department of Physiology, Tulane University School of Medicine, New Orleans, Louisiana, USA.

出版信息

Mol Pharmacol. 2000 Feb;57(2):259-67.

Abstract

The objective of this study was to determine the role of cytoplasmic (protein kinase-like homology and guanylyl cyclase catalytic) domains of atrial natriuretic peptide (ANP) receptor-A (Npra) in postbinding events and metabolic turnover of ligand-receptor complexes. Using deletion mutagenesis, the specific regions in the intracellular domains of Npra relevant to the receptor function, namely ligand-binding, cGMP production, and internalization and sequestration of ligand-receptor complexes, have been determined in transiently expressing COS-7 cells. Deletion of 12 aa (aa) at the carboxyl-terminal end of receptor (Delta1045-Npra) affected neither ligand-binding efficiency nor cGMP production. However, deletion of 120 to 170 aa residues (Delta937-Npra, Delta916-Npra, Delta902-Npra, and Delta887-Npra) decreased ligand binding by 16 to 20% and cGMP production by 50 to 90%. Further deletion of 422 aa and 569 aa (Delta635-Npra and Delta488-Npra) reduced ligand binding efficiency by 40% and 90%, respectively. The deletion of 12 aa (Delta1045-Npra) did not affect the internalization of Npra; however, deletions up to 170 aa (Delta937-Npra, Delta916-Npra, Delta887-Npra) reduced the internalization of ligand-receptor complexes by 60%. Cells expressing either full-length (wild-type) Npra or 120 aa deleted receptor (Delta937-Npra) released 40 to 45% (125)I-ANP radioactivity into culture medium, but only 10 to 15% radioactivity was released from the cells that expressed Delta635-Npra. Furthermore, 35 to 40% (125)I-ANP radioactivity was detected into the intracellular compartments of cells that expressed the wild-type Npra, and only 5 to 10% (125)I-ANP radioactivity was observed in cells expressing the Delta635-Npra (-422 aa) or Delta488-Npra (-569 aa) mutant receptors. These results show that specific regions within the intracellular domains of Npra determine the extent of ligand-binding efficiency, cGMP production, endocytosis, and intracellular sequestration of ligand-receptor complexes in cDNA expressing COS-7 cells.

摘要

本研究的目的是确定心房利钠肽(ANP)受体-A(Npra)的细胞质(蛋白激酶样同源性和鸟苷酸环化酶催化)结构域在配体-受体复合物的结合后事件和代谢周转中的作用。利用缺失诱变技术,在瞬时表达的COS-7细胞中确定了Npra细胞内结构域中与受体功能相关的特定区域,即配体结合、cGMP产生以及配体-受体复合物的内化和隔离。受体羧基末端缺失12个氨基酸(aa)(Delta1045-Npra)既不影响配体结合效率,也不影响cGMP产生。然而,缺失120至170个氨基酸残基(Delta937-Npra、Delta916-Npra、Delta902-Npra和Delta887-Npra)使配体结合减少16%至20%,cGMP产生减少50%至90%。进一步缺失422个氨基酸和569个氨基酸(Delta635-Npra和Delta488-Npra)分别使配体结合效率降低40%和90%。缺失12个氨基酸(Delta1045-Npra)不影响Npra的内化;然而,缺失多达170个氨基酸(Delta937-Npra、Delta916-Npra、Delta887-Npra)使配体-受体复合物的内化减少60%。表达全长(野生型)Npra或缺失120个氨基酸的受体(Delta937-Npra)的细胞将40%至45%的(125)I-ANP放射性释放到培养基中,但表达Delta635-Npra的细胞仅释放10%至15%的放射性。此外,在表达野生型Npra的细胞的细胞内区室中检测到35%至40%的(125)I-ANP放射性,而在表达Delta635-Npra(-422个氨基酸)或Delta488-Npra(-569个氨基酸)突变受体的细胞中仅观察到5%至10%的(125)I-ANP放射性。这些结果表明,Npra细胞内结构域中的特定区域决定了cDNA表达的COS-7细胞中配体结合效率、cGMP产生、内吞作用以及配体-受体复合物的细胞内隔离程度。

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