淋巴细胞中血管活性肠肽的表达:可能在免疫系统调节中的内源性作用

Javier Leceta, Carmen Martínez, Mario Delgado, Elvira Garrido, Rosa P. Gomariz
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引用次数: 60

摘要

越来越多的实验证据表明,血管活性肠肽(VIP)具有免疫调节肽的作用。我们和其他实验室的研究结果表明,免疫系统的细胞能够产生VIP。我们用免疫组织化学方法在中央和周围淋巴器官的特定部位检测了VIP在淋巴细胞中的免疫反应性。双免疫荧光染色和流式细胞术分析表明T淋巴细胞和B淋巴细胞均含有VIP,高效液相色谱和放射免疫分析证实VIP主要为VIP1-28。VIP也通过原位杂交和逆转录以及聚合酶链反应得到证实。我们也检测到有丝分裂刺激后脾淋巴细胞中VIP的诱导。淋巴细胞应该对内源性VIP敏感,因为我们也在不同的淋巴细胞群体中检测到了VIP受体的表达。这些证据表明VIP是一种内源性的免疫功能自分泌调节剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression of vasoactive intestinal peptide in lymphocytes: a possible endogenous role in the regulation of the immune system

Experimental evidence is accumulating showing that vasoactive intestinal peptide (VIP) acts as an immunoregulatory peptide. Findings from our laboratory and others indicate that cells of the immune system are able to produce VIP. We have detected immunoreactivity for VIP in lymphocytes by immunohistochemical methods at specific locations of both central and peripheral lymphoid organs. Double immunofluorescence staining and flow cytometry analysis indicate that both T and B lymphocytes contain VIP that has been proved to be mostly VIP1–28 by high-performance liquid chromatography and radioimmunoassay. VIP has been also demonstrated by ‘in situ’ hybridization and reverse transcription followed by polymerase chain reaction. We have also detected induction of VIP in splenic lymphocytes after mitogenic stimulation. Lymphocytes should be sensitive to the endogenously produced VIP because we have also detected VIP receptor expression in different populations of lymphocytes. All this evidence indicates that VIP is an endogenous autocrine modulator of immune function.

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