Boudard F, Bastide M
Immunology Research Unit, Faculty of Pharmacy, Montpellier, France.
J Neurosci Res. 1991 May;29(1):29-41. doi: 10.1002/jnr.490290104.
We compared the effect of two neuropeptides, calcitonin gene-related peptide (CGRP) and vasoactive intestinal peptide (VIP), on mitogen-induced murine splenocyte proliferation. Both neuropeptides exerted their maximal effect within 24 hr after activation by Con A. The combination CGRP-VIP caused an additive inhibitory effect on T-cell proliferation. The inhibitory effect of VIP could be correlated with a decrease in interleukin 2 (IL-2) production, whereas CGRP did not affect this production. Since we also observed an additive inhibitory effect on T-cell proliferation by the theophylline and CGRP or VIP combination, we measured the effect of each neuropeptide on intracellular cAMP production by enriched T-cells: CGRP, but not VIP, strongly stimulated cAMP synthesis. Taken together, our results indicate that inhibition of murine T-cell proliferation by CGRP and VIP is mediated by different mechanisms.
我们比较了两种神经肽,降钙素基因相关肽(CGRP)和血管活性肠肽(VIP)对丝裂原诱导的小鼠脾细胞增殖的影响。两种神经肽在被刀豆蛋白A激活后的24小时内发挥其最大作用。CGRP-VIP组合对T细胞增殖产生相加抑制作用。VIP的抑制作用可能与白细胞介素2(IL-2)产生的减少有关,而CGRP不影响这种产生。由于我们还观察到茶碱与CGRP或VIP组合对T细胞增殖有相加抑制作用,我们测量了每种神经肽对富集T细胞内cAMP产生的影响:CGRP强烈刺激cAMP合成,而VIP则无此作用。综上所述,我们的结果表明CGRP和VIP对小鼠T细胞增殖的抑制作用是由不同机制介导的。