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小鼠巨噬细胞中G蛋白偶联受体的表达分析。

Expression analysis of G Protein-Coupled Receptors in mouse macrophages.

作者信息

Lattin Jane E, Schroder Kate, Su Andrew I, Walker John R, Zhang Jie, Wiltshire Tim, Saijo Kaoru, Glass Christopher K, Hume David A, Kellie Stuart, Sweet Matthew J

机构信息

Cooperative Research Centre for Chronic Inflammatory Diseases and Special Research Centre for Functional and Applied Genomics, Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland, 4072, Australia.

出版信息

Immunome Res. 2008 Apr 29;4:5. doi: 10.1186/1745-7580-4-5.

Abstract

BACKGROUND

Monocytes and macrophages express an extensive repertoire of G Protein-Coupled Receptors (GPCRs) that regulate inflammation and immunity. In this study we performed a systematic micro-array analysis of GPCR expression in primary mouse macrophages to identify family members that are either enriched in macrophages compared to a panel of other cell types, or are regulated by an inflammatory stimulus, the bacterial product lipopolysaccharide (LPS).

RESULTS

Several members of the P2RY family had striking expression patterns in macrophages; P2ry6 mRNA was essentially expressed in a macrophage-specific fashion, whilst P2ry1 and P2ry5 mRNA levels were strongly down-regulated by LPS. Expression of several other GPCRs was either restricted to macrophages (e.g. Gpr84) or to both macrophages and neural tissues (e.g. P2ry12, Gpr85). The GPCR repertoire expressed by bone marrow-derived macrophages and thioglycollate-elicited peritoneal macrophages had some commonality, but there were also several GPCRs preferentially expressed by either cell population.

CONCLUSION

The constitutive or regulated expression in macrophages of several GPCRs identified in this study has not previously been described. Future studies on such GPCRs and their agonists are likely to provide important insights into macrophage biology, as well as novel inflammatory pathways that could be future targets for drug discovery.

摘要

背景

单核细胞和巨噬细胞表达多种G蛋白偶联受体(GPCRs),这些受体调节炎症和免疫。在本研究中,我们对原代小鼠巨噬细胞中的GPCR表达进行了系统的微阵列分析,以鉴定与一组其他细胞类型相比在巨噬细胞中富集的家族成员,或受炎症刺激物细菌产物脂多糖(LPS)调节的家族成员。

结果

P2RY家族的几个成员在巨噬细胞中具有显著的表达模式;P2ry6 mRNA基本上以巨噬细胞特异性方式表达,而P2ry1和P2ry5 mRNA水平则被LPS强烈下调。其他几种GPCR的表达要么局限于巨噬细胞(如Gpr84),要么局限于巨噬细胞和神经组织(如P2ry12、Gpr85)。骨髓来源的巨噬细胞和巯基乙酸诱导的腹腔巨噬细胞表达的GPCR库有一些共性,但也有几种GPCR优先在任一细胞群体中表达。

结论

本研究中鉴定的几种GPCR在巨噬细胞中的组成性或调节性表达此前尚未见报道。对这类GPCR及其激动剂的进一步研究可能会为巨噬细胞生物学提供重要见解,以及可能成为未来药物发现靶点的新炎症途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1d3/2394514/a7a4eef2a898/1745-7580-4-5-1.jpg

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