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与颈上神经节神经突共培养的骨髓来源肥大细胞中的钙反应和高亲和力IgE受体表达

Calcium response and FcepsilonRI expression in bone marrow-derived mast cells co-cultured with SCG neurites.

作者信息

Suzuki Akio, Suzuki Ryo, Furuno Tadahide, Teshima Reiko, Nakanishi Mamoru

机构信息

Graduate School of Pharmaceutical Sciences, Nagoya City University; Nagoya 467-8603, Japan.

出版信息

Biol Pharm Bull. 2005 Oct;28(10):1963-5. doi: 10.1248/bpb.28.1963.

Abstract

Communication between nerves and mast cells is a prototypic demonstration of neuro-immune interaction. Numerous studies have shown that the stimulation of nerves (or addition of neurotransmitters) can evoke activation of mast cells, and that mast cell-derived mediators can influence neuronal activity. However, it is still unknown whether high affinity IgE receptors (FcepsilonRI) themselves are involved directly in the communication between nerves and mast cells. In the present experiments, we used an in vitro co-culture approach comprising interaction between immune (bone marrow-derived mast cells, BMMCs) and nerve cells (superior cervical ganglia, SCG) to solve the above problem. We found that the intracellular calcium ion concentration ([Ca2+]i) increased much more in BMMCs after antigen (DNP7-BSA) stimulation when they were associated with SCG neurites in the co-culture system. But the [Ca2+]i in BMMCs was less increased when they were not associated with the neurites. Further, the in vitro co-culture approach of BMMCs with SCG neurites for 3 d showed the increases of FcepsilonRI expression occurred on the plasma membranes of BMMCs which were attached to the neurites. On the contrary, N-cadherin molecules which localized on the interface between on the plasma membrane of BMMCs and SCG neurites did not increase with the co-culture for 3 d. All of these results indicated that co-culturing BMMCs with SCG neurites for 3 d promoted not only the calcium response but also the FcepsilonRI expression in BMMCs.

摘要

神经与肥大细胞之间的通讯是神经免疫相互作用的典型例证。大量研究表明,神经刺激(或添加神经递质)可引发肥大细胞的激活,且肥大细胞衍生的介质可影响神经元活动。然而,高亲和力IgE受体(FcepsilonRI)自身是否直接参与神经与肥大细胞之间的通讯仍不清楚。在本实验中,我们采用了一种体外共培养方法,该方法包括免疫细胞(骨髓来源的肥大细胞,BMMCs)与神经细胞(颈上神经节,SCG)之间的相互作用,以解决上述问题。我们发现,在共培养系统中,当抗原(DNP7-BSA)刺激后,与SCG神经突相关的BMMCs细胞内钙离子浓度([Ca2+]i)增加得更多。但当BMMCs与神经突不相关时,其[Ca2+]i增加较少。此外,BMMCs与SCG神经突进行3天的体外共培养后,附着于神经突的BMMCs质膜上FcepsilonRI表达增加。相反,位于BMMCs质膜与SCG神经突界面的N-钙黏蛋白分子在共培养3天时并未增加。所有这些结果表明,BMMCs与SCG神经突共培养3天不仅促进了BMMCs中的钙反应,还促进了其FcepsilonRI表达。

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