UDP acting at P2Y6 receptors is a mediator of microglial phagocytosis

被引:0
|
作者
Schuichi Koizumi
Yukari Shigemoto-Mogami
Kaoru Nasu-Tada
Yoichi Shinozaki
Keiko Ohsawa
Makoto Tsuda
Bhalchandra V. Joshi
Kenneth A. Jacobson
Shinichi Kohsaka
Kazuhide Inoue
机构
[1] National Institute of Health Sciences,Division of Pharmacology
[2] 1-18-1 Kamiyoga,Department of Pharmacology
[3] Setagaya,Department of Molecular and System Pharmacology
[4] Tokyo 158-8501,Department of Neurochemistry
[5] Japan,undefined
[6] Interdisciplinary Graduate School of Medicine and Engineering,undefined
[7] University of Yamanashi,undefined
[8] 1110 Shimokato,undefined
[9] Chuo,undefined
[10] Yamanashi 409-3893,undefined
[11] Japan,undefined
[12] Graduate School of Pharmaceutical Sciences,undefined
[13] Kyushu University,undefined
[14] 3-1-1 Maidashi,undefined
[15] Higashi,undefined
[16] Fukuoka 812-8582,undefined
[17] Japan,undefined
[18] National Institute of Neuroscience,undefined
[19] 4-1-1 Ogawahigashi,undefined
[20] Kodaira,undefined
[21] Tokyo 187-8502,undefined
[22] Japan,undefined
[23] Molecular Recognition Section,undefined
[24] Laboratory of Bioorganic Chemistry,undefined
[25] National Institute of Diabetes and Digestive and Kidney Diseases,undefined
[26] National Institutes of Health,undefined
[27] Bethesda,undefined
[28] Maryland 20892-0810,undefined
[29] USA,undefined
来源
Nature | 2007年 / 446卷
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摘要
Phagocytosis is thought to be initiated by activation of phagocytosis-promoting receptors that recognize 'eat-me' signals such as phosphatidylserine or amyloid-β expressed in the apoptotic cells. But now Koizumi et al. demonstrate a novel type of microglial phagocytosis that requires neither typical 'eat-me' signals nor Fc receptor ligands for initiation. Instead, this phagocytosis is promoted by the diffusible extracellular molecule uridine 5′-diphosphate, released by injured cells. The UDP activates P2Y6 receptors on the microglial surface. The clearance of dead cells is crucial to the maintenance of brain function, so these findings may have implications for a range of central nervous system diseases.
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页码:1091 / 1095
页数:4
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