Suppr超能文献

小鼠白细胞介素-13受体α2:分子克隆、特性鉴定及其与小鼠白细胞介素-13受体α1的比较。

The murine IL-13 receptor alpha 2: molecular cloning, characterization, and comparison with murine IL-13 receptor alpha 1.

作者信息

Donaldson D D, Whitters M J, Fitz L J, Neben T Y, Finnerty H, Henderson S L, O'Hara R M, Beier D R, Turner K J, Wood C R, Collins M

机构信息

Genetics Institute, Immunology Department, Cambridge, MA 02140, USA.

出版信息

J Immunol. 1998 Sep 1;161(5):2317-24.

PMID:9725226
Abstract

Two components of a receptor complex for IL-13, the IL-4R and a low affinity IL-13-binding chain, IL-13R alpha 1, have been cloned in mice and humans. An additional high affinity binding chain for IL-13, IL-13R alpha 2, has been described in humans. We isolated a cDNA from the thymus that encodes the murine orthologue of the human IL-13R alpha 2. The predicted protein sequence of murine IL-13R alpha 2 (mIL-13R alpha 2) has 59% overall identity to human IL-13R alpha 2 and is closely related to the murine low affinity IL-13-binding subunit, IL-13R alpha 1. The genes for both mIL-13-binding chains map to the X chromosome. A specific interaction between mIL-13R alpha 2.Fc protein and IL-13 was demonstrated by surface plasmon resonance using a BIACORE instrument. Ba/F3 cells that were transfected with mIL-13R alpha 2 expressed 5000 molecules per cell and bound IL-13 with a single Kd of 0.5 to 1.2 nM. However, these cells did not proliferate in response to IL-13, and the IL-4 dose response was unaffected by high concentrations of IL-13. In contrast, the expression of mIL-13R alpha 1 by Ba/F3 cells resulted in a sensitive proliferative response to IL-13. Consistent with its lower affinity for IL-13, IL-13R alpha 1.Fc was 100-fold less effective than IL-13R alpha 2.Fc in neutralizing IL-13 in vitro. These results show that mIL-13R alpha 2 and mIL-13R alpha 1 are not functionally equivalent and predict distinct roles for each polypeptide in IL-13R complex formation and in the modulation of IL-13 signal transduction.

摘要

白细胞介素-13(IL-13)受体复合物的两个组分,即IL-4受体和低亲和力IL-13结合链IL-13Rα1,已在小鼠和人类中克隆出来。人类中还发现了另一种IL-13的高亲和力结合链IL-13Rα2。我们从胸腺中分离出一个cDNA,它编码人类IL-13Rα2的小鼠同源物。小鼠IL-13Rα2(mIL-13Rα2)的预测蛋白序列与人类IL-13Rα2的总体一致性为59%,并且与小鼠低亲和力IL-13结合亚基IL-13Rα1密切相关。两种mIL-13结合链的基因都定位于X染色体。使用BIACORE仪器通过表面等离子体共振证明了mIL-13Rα2.Fc蛋白与IL-13之间存在特异性相互作用。用mIL-13Rα2转染的Ba/F3细胞每个细胞表达5000个分子,并且以0.5至1.2 nM的单一解离常数(Kd)结合IL-13。然而,这些细胞对IL-13没有增殖反应,并且IL-4剂量反应不受高浓度IL-13的影响。相比之下,Ba/F3细胞表达mIL-13Rα1会导致对IL-13产生敏感的增殖反应。与其对IL-13的较低亲和力一致,IL-13Rα1.Fc在体外中和IL-13的效果比IL-13Rα2.Fc低100倍。这些结果表明,mIL-13Rα2和mIL-13Rα1在功能上不等同,并预测每种多肽在IL-13受体复合物形成和IL-13信号转导调节中具有不同的作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验