Dijkstra Dorothea, Leurs Rob, Chazot Paul, Shenton Fiona C, Stark Holger, Werfel Thomas, Gutzmer Ralf
Department of Dermatology and Allergology, Hannover Medical University, Hannover, Germany.
J Allergy Clin Immunol. 2007 Aug;120(2):300-7. doi: 10.1016/j.jaci.2007.03.024. Epub 2007 May 15.
The expression of the recently cloned histamine H(4) receptor (H(4)R) by leukocytes suggests a role in immunomodulation.
The expression and function of the H(4)R on human monocytes obtained from peripheral blood was investigated.
H(4)R expression was studied by using flow cytometry. Effects of H(4)R stimulation on Ca(2+) mobilization was determined fluorometrically, CCL2 production was determined by means of ELISA, intracellular CCL2 staining was measured with flow cytometry, and CCL2 mRNA was measured by using real-time quantitative LightCycler PCR. The relevance of CCL2 production was determined in chemotaxis transmigration assays.
H(4)R protein was expressed by monocytes and upregulated by IFN-gamma. H(4)R agonists (clobenpropit and 4-methylhistamine) induce a Ca(2+) mobilization in monocytes, which could be blocked with the selective H(4)R antagonist JNJ7,777,120. Furthermore, H(4)R agonists downregulated CCL2 protein production. This effect could also be blocked by JNJ7,777,120. Supernatants of H(4)R agonist-stimulated monocytes attracted less monocytes in transmigration assays. The downregulation of CCL2 production was regulated at different levels. First, the synthesis of CCL2 mRNA was significantly decreased. Second, intracellular staining suggested an inhibition of CCL2 secretion after stimulation with H(4)R agonists.
Human monocytes express the H(4)R, and its stimulation leads to a Ca(2+) influx and an inhibition of CCL2 production, resulting in a reduction of monocyte recruitment.
The H(4)R could represent an important anti-inflammatory receptor on monocytes and could be an interesting target for drug development.
白细胞中最近克隆的组胺H4受体(H4R)的表达提示其在免疫调节中发挥作用。
研究外周血来源的人单核细胞上H4R的表达及功能。
采用流式细胞术研究H4R表达。通过荧光法测定H4R激动剂对钙离子动员的影响,采用酶联免疫吸附测定法测定CCL2生成,用流式细胞术检测细胞内CCL2染色,并用实时定量LightCycler PCR法测定CCL2 mRNA。在趋化迁移试验中确定CCL2生成的相关性。
单核细胞表达H4R蛋白,且经γ干扰素上调。H4R激动剂(氯苯丙哌嗪和4-甲基组胺)可诱导单核细胞内钙离子动员,这可被选择性H4R拮抗剂JNJ7777120阻断。此外,H4R激动剂下调CCL2蛋白生成。此效应也可被JNJ7777120阻断。在迁移试验中,H4R激动剂刺激的单核细胞培养上清吸引的单核细胞较少。CCL2生成的下调在不同水平受到调控。首先,CCL2 mRNA的合成显著减少。其次,细胞内染色提示H4R激动剂刺激后CCL2分泌受到抑制。
人单核细胞表达H4R,其激动可导致钙离子内流并抑制CCL2生成,从而减少单核细胞募集。
H4R可能是单核细胞上一种重要的抗炎受体,可能是药物研发的一个有意义的靶点。