Svetlana B Krasnova, Natalia V Malkova, Yuliya A Kovalitskaya, Yuri A Zolotarev, Tatyana A Zargarova, Alexander A Kolobov, Elena A Kampe-Nemm, Elena V Navolotskaya, Valery M Lipkin
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引用次数: 0
摘要
结果表明,β -内啡肽和与人IgG重链364-373氨基酸序列相对应的合成十肽SLTCLVKGFY(称为免疫球蛋白)能够刺激人t淋巴母细胞样细胞系Jurkat的生长。阿片受体拮抗剂纳洛酮不抑制肽的刺激作用。[(3)H]-immunorphin与Jurkat细胞受体结合的研究表明,它与纳洛酮不敏感受体结合具有高亲和力(K(d) = 1.3 nM;N = 5.2 x 10(5))。未标记的β -内啡肽和免疫啡肽6-10片段完全抑制T淋巴细胞上标记配体与纳洛酮不敏感受体的特异性结合(K(i)分别= 1.4 x 10(-7)和3.7 x 10(-5) M)。因此,-内啡肽和免疫啡肽在人t淋巴母细胞样细胞系Jurkat上共享纳洛酮不敏感受体。
The Stimulating Effect of the beta-Endorphin-Like Peptide Immunorphin on the Human T-Lymphoblastoid Cell Line Jurkat Is Mediated by a Non-Opioid Receptor for beta-Endorphin.
It was shown that beta-endorphin and the synthetic decapeptide SLTCLVKGFY that corresponds to the amino acid sequence 364-373 of the human IgG heavy chain (referred to as immunorphin) is able to stimulate growth of the human T-lymphoblastoid cell line Jurkat. The antagonist of opioid receptors naloxone did not inhibit the stimulating effect of the peptides. Studies on [(3)H]-immunorphin binding to Jurkat cell receptors have demonstrated that it binds with high affinity to naloxone-insensitive receptors (K(d) = 1.3 nM; n = 5.2 x 10(5)). Unlabeled beta-endorphin and the 6-10 fragment of immunorphin completely inhibited the labeled ligand specific binding to naloxone-insensitive receptors on T lymphocytes (K(i) = 1.4 x 10(-7) and 3.7 x 10(-5) M, respectively). Thus, beta-endorphin and immunorphin share the naloxone-insensitive receptors on human T-lymphoblastoid cell line Jurkat.