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核苷酸、腺苷及其受体调节趋化作用的新见解。

New insights regarding the regulation of chemotaxis by nucleotides, adenosine, and their receptors.

机构信息

Institute of Cell Signalling, University of Nottingham, Nottingham, UK.

出版信息

Purinergic Signal. 2012 Sep;8(3):587-98. doi: 10.1007/s11302-012-9311-x. Epub 2012 Apr 15.

DOI:10.1007/s11302-012-9311-x
PMID:22528684
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3360098/
Abstract

The directional movement of cells can be regulated by ATP, certain other nucleotides (e.g., ADP, UTP), and adenosine. Such regulation occurs for cells that are "professional phagocytes" (e.g., neutrophils, macrophages, certain lymphocytes, and microglia) and that undergo directional migration and subsequent phagocytosis. Numerous other cell types (e.g., fibroblasts, endothelial cells, neurons, and keratinocytes) also change motility and migration in response to ATP, other nucleotides, and adenosine. In this article, we review how nucleotides and adenosine modulate chemotaxis and motility and highlight the importance of nucleotide- and adenosine-regulated cell migration in several cell types: neutrophils, microglia, endothelial cells, and cancer cells. We also discuss difficulties in conducting experiments and drawing conclusions regarding the ability of nucleotides and adenosine to modulate the migration of professional and non-professional phagocytes.

摘要

细胞的定向运动可以被 ATP、某些其他核苷酸(如 ADP、UTP)和腺苷调节。这种调节发生在“专业吞噬细胞”(如中性粒细胞、巨噬细胞、某些淋巴细胞和小胶质细胞)中,它们会发生定向迁移和随后的吞噬作用。许多其他细胞类型(如成纤维细胞、内皮细胞、神经元和角质细胞)也会响应 ATP、其他核苷酸和腺苷改变其运动性和迁移性。在本文中,我们回顾了核苷酸和腺苷如何调节趋化性和运动性,并强调了核苷酸和腺苷调节几种细胞类型(如中性粒细胞、小胶质细胞、内皮细胞和癌细胞)中细胞迁移的重要性。我们还讨论了在进行实验和得出关于核苷酸和腺苷调节专业和非专业吞噬细胞迁移能力的结论方面存在的困难。

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本文引用的文献

1
Vesicular and conductive mechanisms of nucleotide release.核苷酸释放的囊泡和传导机制。
Purinergic Signal. 2012 Sep;8(3):359-73. doi: 10.1007/s11302-012-9304-9. Epub 2012 Apr 12.
2
Real-time imaging reveals that P2Y2 and P2Y12 receptor agonists are not chemoattractants and macrophage chemotaxis to complement C5a is phosphatidylinositol 3-kinase (PI3K)- and p38 mitogen-activated protein kinase (MAPK)-independent.实时成像显示,P2Y2 和 P2Y12 受体激动剂不是趋化因子,而补体 C5a 诱导的巨噬细胞趋化作用与磷脂酰肌醇 3-激酶(PI3K)和 p38 丝裂原活化蛋白激酶(MAPK)无关。
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Extracellular ATP acts on P2Y2 purinergic receptors to facilitate HIV-1 infection.细胞外 ATP 通过 P2Y2 嘌呤能受体发挥作用,促进 HIV-1 感染。
J Exp Med. 2011 Aug 29;208(9):1823-34. doi: 10.1084/jem.20101805. Epub 2011 Aug 22.
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A3 adenosine receptor agonist reduces brain ischemic injury and inhibits inflammatory cell migration in rats.A3 腺苷受体激动剂可减少大鼠脑缺血损伤并抑制炎性细胞迁移。
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Extracellular ATP induces CD44 shedding from macrophage-like P388D1 cells via the P2X7 receptor.细胞外 ATP 通过 P2X7 受体诱导巨噬样 P388D1 细胞释放 CD44。
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Chemotaxis in cancer.癌症中的趋化作用。
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