Molecular properties of apelin: tissue distribution and receptor binding

Molecular properties of apelin: tissue distribution and receptor binding
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DOI:
10.1016/s0167-4889(00)00143-9
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发表时间:
2001-04-23
影响因子:
5.1
通讯作者:
Fujino, M
Fujino, M
中科院分区:
生物学2区
文献类型:
--
作者:
Kawamata, Y;Fukusumi, S;Fujino, M

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我们通过定量逆转录-聚合酶链反应分析了大鼠apelin mRNA的组织分布,并通过使用单克隆抗体的酶免疫测定法(EIA)分析了免疫反应性apelin(IR-apelin)的组织分布。apelin mRNA和ir-apelin的表达水平在组织间似乎是一致的:它们在肺和乳腺中高度表达。通过凝胶过滤和EIA的组合,nle发现apelin的分子形式在各个组织中不同:大小接近apelin-36(长型)的apelin分子是肺、睾丸和子宫中的主要组分,但在乳腺中检测到长型和短型(其大小接近[Glu(65)]apelin-13)。在Scatchard分析中,放射性碘标记的爱帕琳-36类似物与受体结合。APJ,具有高亲和力。在竞争性结合测定中,爱帕琳-36和爱帕琳-19比[Glu(65)]爱帕琳-13更有效地抑制标记的爱帕琳-36类似物与APJ的结合。在爱帕琳从APJ解离的分析中,未标记的爱帕琳-36比[Glu(65)]爱帕琳-13更快地取代与APJ结合的标记的爱帕琳-36类似物。我们的研究结果表明,长和短形式的爱帕琳不同地与APJ相互作用。 Elsevier Science B. V.保留所有权利。
We analyzed the tissue distribution of apelin mRNA in rats by a quantitative revere transcription-polymerase chain reaction and that of immunoreactive apelin (ir-apelin) by an enzyme immunoassay (EIA) using a monoclonal antibody. The expression levels of apelin mRNA and ir-apelin seemed to be consistent among tissues: they were highly expressed in the lung and mammary gland. By the combination of gel filtration and EIA, nle found that the molecular forms of apelin differ among respective tissues: apelin molecules with sizes close to apelin-36 (long forms) were major components ill the lung, testis, and uterus, but both long and short (whose sizes were close to [< Glu(65)]apelin-13) forms were detected in the mammary gland. In Scatchard analyses, the radioiodinated apelin-36 analogue bound to the receptor. APJ, with high affinity. In competitive binding assays, apelin-36 and apelin-19 far more efficiently inhibited the binding of the labeled apelin-36 analogue with APJ than [< Glu(65)]apelin-13. In analyses for the dissociation of apelin from APJ, unlabeled apelin-36 replaced mole rapidly the labeled apelin-36 analogue bound with APJ than [ < Glu(65)]apelin-13. Our results demonstrate that the long and short forms of apelin differently interact with APJ. Elsevier Science B.V. All rights reserved.