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小鼠淋巴细胞中血管活性肠肽受体1和2(VIP-R1和VIP-R2)mRNA的差异表达

Differential expression of vasoactive intestinal peptide receptors 1 and 2 (VIP-R1 and VIP-R2) mRNA in murine lymphocytes.

作者信息

Delgado M, Martinez C, Johnson M C, Gomariz R P, Ganea D

机构信息

Department of Biological Sciences, Rutgers University, Newark, NJ 07102, USA.

出版信息

J Neuroimmunol. 1996 Aug;68(1-2):27-38. doi: 10.1016/0165-5728(96)00063-x.

Abstract

Vasoactive intestinal peptide (VIP), a neuropeptide present in the lymphoid microenvironment, modulates cytokine expression and affects T cell proliferation. Recent molecular studies identified two VIP receptors. VIP-R1 and VIP-R2, primarily in nonlymphoid cells. In this study, we investigate the expression of VIP-R1 and VIP-R2 mRNA in unstimulated and stimulated lymphocytes and thymocytes, and in various lymphocyte subpopulations. In contrast to VIP-R1 which is constitutively expressed, the expression of VIP-R2 is induced only following stimulation through the TCR-associated CD3 complex. Both CD4+ and CD8+ T cells express VIP-R1 and VIP-R2. Two T cell lines, EL-4.IL-2 and D10.G4.1 express exclusively VIP-R2. VIP induces the expression of the VIP-R2 gene in the absence of additional stimuli. Differential expression and regulation of the two VIP receptors in T lymphocytes suggests different physiological roles in mediating the immunomodulatory activities of VIP and related neuropeptides.

摘要

血管活性肠肽(VIP)是一种存在于淋巴微环境中的神经肽,可调节细胞因子表达并影响T细胞增殖。最近的分子研究鉴定出两种VIP受体,即VIP-R1和VIP-R2,主要存在于非淋巴细胞中。在本研究中,我们调查了VIP-R1和VIP-R2 mRNA在未刺激和刺激的淋巴细胞及胸腺细胞以及各种淋巴细胞亚群中的表达情况。与组成性表达的VIP-R1不同,VIP-R2仅在通过TCR相关的CD3复合物刺激后才被诱导表达。CD4 +和CD8 + T细胞均表达VIP-R1和VIP-R2。两种T细胞系EL-4.IL-2和D10.G4.1仅表达VIP-R2。在没有额外刺激的情况下,VIP可诱导VIP-R2基因的表达。T淋巴细胞中两种VIP受体的差异表达和调节表明它们在介导VIP和相关神经肽的免疫调节活性中具有不同的生理作用。

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