The P2Y12 receptor regulates microglial activation by extracellular nucleotides

• Published in: Nature neuroscience Vol. 9; no. 12; pp. 1512 - 1519
• Main Authors: Haynes, Sharon E, Hollopeter, Gunther, Yang, Guang, Kurpius, Dana, Dailey, Michael E, Gan, Wen-Biao, Julius, David
• Format: Journal Article
• Language: English
• Published: United States Nature Publishing Group 01.12.2006
• Subjects: Adenosine Diphosphate - physiology; Adenosine Diphosphate - secretion; Adenosine Triphosphate - physiology; Adenosine Triphosphate - secretion; Animals; Brain Injuries - immunology; Brain Injuries - metabolism; Cell receptors; Cellular signal transduction; Central Nervous System - cytology; Central Nervous System - immunology; Chemotaxis - physiology; Injuries; Membrane Proteins - immunology; Membrane Proteins - metabolism; Mice; Mice, Knockout; Microglia - immunology; Microglia - metabolism; Morphology; Neuroglia; Neurosciences; Nucleotides; Physiological aspects; Physiology; Proteins; Receptors, Purinergic P2 - immunology; Receptors, Purinergic P2 - metabolism; Receptors, Purinergic P2Y12; Spinal cord; United States; New York; San Francisco California; California; United States > US
• ISSN: 1097-6256; 1546-1726
• DOI: 10.1038/nn1805

Microglia are primary immune sentinels of the CNS. Following injury, these cells migrate or extend processes toward sites of tissue damage. CNS injury is accompanied by release of nucleotides, serving as signals for microglial activation or chemotaxis. Microglia express several purinoceptors, including a G(i)-coupled subtype that has been implicated in ATP- and ADP-mediated migration in vitro. Here we show that microglia from mice lacking G(i)-coupled P2Y(12) receptors exhibit normal baseline motility but are unable to polarize, migrate or extend processes toward nucleotides in vitro or in vivo. Microglia in P2ry(12)(-/-) mice show significantly diminished directional branch extension toward sites of cortical damage in the living mouse. Moreover, P2Y(12) expression is robust in the 'resting' state, but dramatically reduced after microglial activation. These results imply that P2Y(12) is a primary site at which nucleotides act to induce microglial chemotaxis at early stages of the response to local CNS injury.