Microglia modulate blood flow, neurovascular coupling, and hypoperfusion via purinergic actions

• Published in: The Journal of experimental medicine Vol. 219; no. 3
• Main Authors: Császár, Eszter, Lénárt, Nikolett, Cserép, Csaba, Környei, Zsuzsanna, Fekete, Rebeka, Pósfai, Balázs, Balázsfi, Diána, Hangya, Balázs, Schwarcz, Anett D, Szabadits, Eszter, Szöllősi, Dávid, Szigeti, Krisztián, Máthé, Domokos, West, Brian L, Sviatkó, Katalin, Brás, Ana Rita, Mariani, Jean-Charles, Kliewer, Andrea, Lenkei, Zsolt, Hricisák, László, Benyó, Zoltán, Baranyi, Mária, Sperlágh, Beáta, Menyhárt, Ákos, Farkas, Eszter, Dénes, Ádám
• Format: Journal Article
• Language: English
• Published: United States Rockefeller University Press 07-03-2022
• Subjects: Adult; Aged; Animals; Brain - physiology; Calcium Signaling - physiology; Carotid Artery Diseases - physiopathology; Cerebrovascular Circulation - physiology; Evoked Potentials - physiology; Female; Humans; Hypercapnia - physiopathology; Life Sciences; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Microglia - physiology; Neuroinflammation; Neurons and Cognition; Neuroscience; Neurovascular Coupling - physiology; Receptors, Purinergic - physiology; Receptors, Purinergic P2Y12 - physiology; Vasodilation - physiology; Vibrissae - innervation
• ISSN: 0022-1007; 1540-9538; 1540-9538
• DOI: 10.1084/jem.20211071

Microglia, the main immunocompetent cells of the brain, regulate neuronal function, but their contribution to cerebral blood flow (CBF) regulation has remained elusive. Here, we identify microglia as important modulators of CBF both under physiological conditions and during hypoperfusion. Microglia establish direct, dynamic purinergic contacts with cells in the neurovascular unit that shape CBF in both mice and humans. Surprisingly, the absence of microglia or blockade of microglial P2Y12 receptor (P2Y12R) substantially impairs neurovascular coupling in mice, which is reiterated by chemogenetically induced microglial dysfunction associated with impaired ATP sensitivity. Hypercapnia induces rapid microglial calcium changes, P2Y12R-mediated formation of perivascular phylopodia, and microglial adenosine production, while depletion of microglia reduces brain pH and impairs hypercapnia-induced vasodilation. Microglial actions modulate vascular cyclic GMP levels but are partially independent of nitric oxide. Finally, microglial dysfunction markedly impairs P2Y12R-mediated cerebrovascular adaptation to common carotid artery occlusion resulting in hypoperfusion. Thus, our data reveal a previously unrecognized role for microglia in CBF regulation, with broad implications for common neurological diseases.