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星形胶质细胞和小胶质细胞中 2',3'-cAMP-腺苷途径的表达。

Expression of the 2',3'-cAMP-adenosine pathway in astrocytes and microglia.

机构信息

Departments of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15219, USA.

出版信息

J Neurochem. 2011 Sep;118(6):979-87. doi: 10.1111/j.1471-4159.2011.07392.x. Epub 2011 Aug 12.

DOI:10.1111/j.1471-4159.2011.07392.x
PMID:21777245
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3166383/
Abstract

Many organs express the extracellular 3',5'-cAMP-adenosine pathway (conversion of extracellular 3',5'-cAMP to 5'-AMP and 5'-AMP to adenosine). Some organs release 2',3'-cAMP (isomer of 3',5'-cAMP) and convert extracellular 2',3'-cAMP to 2'- and 3'-AMP and convert these AMPs to adenosine (extracellular 2',3'-cAMP-adenosine pathway). As astrocytes and microglia are important participants in the response to brain injury and adenosine is an endogenous neuroprotectant, we investigated whether these extracellular cAMP-adenosine pathways exist in these cell types. 2',3'-, 3',5'-cAMP, 5'-, 3'-, and 2'-AMP were incubated with mouse primary astrocytes or primary microglia for 1 h and purine metabolites were measured in the medium by mass spectrometry. There was little evidence of a 3',5'-cAMP-adenosine pathway in either astrocytes or microglia. In contrast, both cell types converted 2',3'-cAMP to 2'- and 3'-AMP (with 2'-AMP being the predominant product). Although both cell types converted 2'- and 3'-AMP to adenosine, microglia were five- and sevenfold, respectively, more efficient than astrocytes in this regard. Inhibitor studies indicated that the conversion of 2',3'-cAMP to 2'-AMP was mediated by a different ecto-enzyme than that involved in the metabolism of 2',3'-cAMP to 3'-AMP and that although CD73 mediates the conversion of 5'-AMP to adenosine, an alternative ecto-enzyme metabolizes 2'- or 3'-AMP to adenosine.

摘要

许多器官表达细胞外 3',5'-cAMP-腺苷途径(将细胞外 3',5'-cAMP 转化为 5'-AMP 和 5'-AMP 转化为腺苷)。一些器官释放 2',3'-cAMP(3',5'-cAMP 的异构体)并将细胞外 2',3'-cAMP 转化为 2'-和 3'-AMP,并将这些 AMP 转化为腺苷(细胞外 2',3'-cAMP-腺苷途径)。由于星形胶质细胞和小胶质细胞是对脑损伤反应的重要参与者,而腺苷是内源性神经保护剂,我们研究了这些细胞类型是否存在这些细胞外 cAMP-腺苷途径。将 2',3' - ,3',5'-cAMP,5' - ,3' - ,和 2'-AMP 与小鼠原代星形胶质细胞或原代小胶质细胞孵育 1 小时,并通过质谱法测量培养基中的嘌呤代谢物。在星形胶质细胞或小胶质细胞中几乎没有 3',5'-cAMP-腺苷途径的证据。相比之下,两种细胞类型都将 2',3'-cAMP 转化为 2'-和 3'-AMP(以 2'-AMP 为主产物)。尽管两种细胞类型都将 2'-和 3'-AMP 转化为腺苷,但小胶质细胞在这方面的效率分别比星形胶质细胞高五倍和七倍。抑制剂研究表明,2',3'-cAMP 转化为 2'-AMP 是由不同于参与 2',3'-cAMP 代谢为 3'-AMP 的不同ecto-酶介导的,尽管 CD73 介导 5'-AMP 转化为腺苷,但替代ecto-酶将 2'-或 3'-AMP 代谢为腺苷。

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