| RRC ID |
85456
|
| Author |
Vittani M, Herlo R, Wang X, Christensen MDB, Vo CT, Mishima T, Kusk P, Konno A, Hirai H, Tsuboi T, Kitaguchi T, Kjaerby C, Asiminas A, Yokoyama T, Sakamoto M, Nedergaard M, Hirase H.
|
| Title |
Cerebral blood flow is modulated by astrocytic cAMP elevation independently of IP3R2-mediated Ca2+ signaling in mice.
|
| Journal |
Proc Natl Acad Sci U S A
|
| Abstract |
Local neural activation drives regional increase of cerebral blood flow (CBF), in a phenomenon known as functional hyperemia. Astrocytes, which enwrap cerebral blood vessels and respond to neuronal activity through their G protein-coupled receptors (GPCRs), play a vital role in brain energy metabolism. Although astrocytic calcium (Ca2+) signaling has been widely studied in relation to neurovascular coupling, the role of cyclic adenosine monophosphate (cAMP), another key second messenger of GPCRs, on CBF has not been established. In this study, we explored the effects of optogenetically induced astrocytic cAMP elevation on CBF. We engineered adeno-associated viral vectors (AAVs) to express a bacterial photoactivated adenylyl cyclase in astrocytes, which triggers an increase in cAMP upon blue light stimulation. Opto-stimulation also elevated astrocytic Ca2+, albeit with a delayed onset under mild stimulation. In vivo imaging of anesthetized and awake wild-type mice through a thinned skull preparation revealed that optogenetically induced astrocytic cAMP elevation led to pronounced arteriole dilation, with a latency of 1.8 s and maximal dilation reached within 10 s in the awake state and slower response under anesthesia. Mild opto-stimulation causing sensory-level cAMP elevations was sufficient to induce arteriole dilation. This effect was preserved in IP3 receptor type 2-knockout (IP3R2-/-) mice, indicating a mechanism independent of GPCR-induced intracellular Ca2+ elevations. These findings highlight astrocytic cAMP as a key modulator of cerebral vasodilation, contributing to our understanding of local CBF regulation. This study opens broad avenues for understanding astrocyte-mediated control of CBF and its implications in neurological diseases characterized by dysregulated blood flow.
|
| Volume |
122(27)
|
| Pages |
e2422069122
|
| Published |
2025-7-8
|
| DOI |
10.1073/pnas.2422069122
|
| PMID |
40591593
|
| PMC |
PMC12260423
|
| MeSH |
Animals
Astrocytes* / metabolism
Calcium / metabolism
Calcium Signaling* / physiology
Cerebrovascular Circulation* / physiology
Cyclic AMP* / metabolism
Inositol 1,4,5-Trisphosphate Receptors* / genetics
Inositol 1,4,5-Trisphosphate Receptors* / metabolism
Male
Mice
Mice, Inbred C57BL
Optogenetics
|
| IF |
9.412
|
| Resource |
| Mice |
RBRC05450
RBRC10289 |
