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一种针对哺乳动物血管紧张素II AT1受体的单克隆抗体识别鳗鱼(欧洲鳗鲡)表达的血管紧张素II受体亚型之一。

A monoclonal antibody to mammalian angiotensin II AT1 receptor recognizes one of the angiotensin II receptor isoforms expressed by the eel (Anguilla anguilla).

作者信息

Marsigliante S, Muscella A, Vilella S, Nicolardi G, Ingrosso L, Ciardo V, Zonno V, Vinson G P, Ho M M, Storelli C

机构信息

Dipartimento di Biologia, Università di Lecce, Italy.

出版信息

J Mol Endocrinol. 1996 Feb;16(1):45-56. doi: 10.1677/jme.0.0160045.

Abstract

Using labelled ligand-binding methods, previous studies have identified specific angiotensin II receptors (Ang II-Rs) in eel liver, kidney and intestine membranes. Isoelectric focusing on polyacrylamide gels also showed that there are two Ang II-R isoforms in eel liver, focusing at isoelectric points (pI) 6.5 and 6.7. These may have different functions. In contrast, eel enterocyte plasma membrane and renal brush border membranes contain only the pI 6.5 form. To characterize the eel receptors more fully, a newly developed monoclonal antibody (6313/G2) which selectively recognizes the AT1 subtype of mammalian Ang II-R was used. In ligand-binding experiments, the preincubation of eel liver membranes with 6313/G2 antibody eliminated the specific [3,5-3H]Tyr4-Ile5-Ang II binding. Moreover, Ang II-receptor complexes from solubilized liver membranes, which were immunoprecipitated by 6313/G2-coated beads, had a pI of 6.5. In immunoblotting experiments, the antibody recognized the isoform focusing at pI 6.5 in eel intestine and liver preparations, but not the liver pI 6.7 isoform. Immunoblotting of SDS gels showed that the antibody bound to a single protein of molecular mass of 75 kDa in eel liver, gill and kidney and to a doublet of molecular mass of about 74 and 75 kDa in intestinal membrane preparations. Immunocytochemistry of paraffin-embedded and cryostat sections of eel liver, kidney, intestine and gill showed that antibody 6313/G2 bound to uniformly distributed intracellular sites and cell surface membranes in proximal tubular cells, absorptive intestinal cells, hepatocytes and chloride cells. It also stained endothelium and both the longitudinal and circular layers of smooth muscle cells in the intestine. The data suggest that the previously described Ang II-R from eel liver, kidney and intestine may be similar to the mammalian AT1 subtype.

摘要

以往的研究运用标记配体结合方法,在鳗鱼肝脏、肾脏和肠膜中鉴定出了特定的血管紧张素II受体(Ang II-Rs)。在聚丙烯酰胺凝胶上进行等电聚焦也显示,鳗鱼肝脏中有两种Ang II-R同工型,聚焦在等电点(pI)6.5和6.7。它们可能具有不同的功能。相比之下,鳗鱼肠上皮细胞质膜和肾刷状缘膜仅含有pI 6.5的形式。为了更全面地表征鳗鱼受体,使用了一种新开发的单克隆抗体(6313/G2),该抗体可选择性识别哺乳动物Ang II-R的AT1亚型。在配体结合实验中,鳗鱼肝膜与6313/G2抗体预孵育消除了特异性的[3,5-3H]Tyr4-Ile5-Ang II结合。此外,由包被有6313/G2的珠子免疫沉淀的溶解肝膜中的Ang II受体复合物,其pI为6.5。在免疫印迹实验中,该抗体识别鳗鱼肠和肝制剂中聚焦在pI 6.5的同工型,但不识别肝pI 6.7的同工型。SDS凝胶免疫印迹显示,该抗体与鳗鱼肝脏、鳃和肾脏中分子量为75 kDa的单一蛋白质结合,并与肠膜制剂中分子量约为74和75 kDa的双峰结合。对鳗鱼肝脏、肾脏、肠和鳃的石蜡包埋切片和低温恒温器切片进行免疫细胞化学分析表明,抗体6313/G2与近端肾小管细胞、吸收性肠细胞、肝细胞和氯化物细胞中均匀分布的细胞内位点和细胞表面膜结合。它还对肠中的内皮以及平滑肌细胞的纵层和环层进行染色。数据表明,先前描述的来自鳗鱼肝脏、肾脏和肠的Ang II-R可能与哺乳动物的AT1亚型相似。

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