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

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...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Császár Eszter
Lénárt Nikolett
Cserép Csaba
Környei Zsuzsanna
Fekete Rebeka
Pósfai Balázs
Balázsfi Diána
Hangya Balázs
Schwarcz Dóra Anett
Cserépné Szabadits Eszter
Szöllősi Dávid
Szigeti Krisztián
Máthé Domokos
West Brian L.
Tóthné 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
Dokumentumtípus: Cikk
Megjelent: 2022
Sorozat:JOURNAL OF EXPERIMENTAL MEDICINE 219 No. 3
Tárgyszavak:
doi:10.1084/jem.20211071

mtmt:32710992
Online Access:http://publicatio.bibl.u-szeged.hu/25659
Leíró adatok
Tartalmi kivonat: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.
Terjedelem/Fizikai jellemzők:33
ISSN:0022-1007