| Autor: |
Lim, Xin Rui, Abd-Alhaseeb, Mohammad M., Ippolito, Michael, Koide, Masayo, Senatore, Amanda J., Plante, Curtis, Hariharan, Ashwini, Weir, Nick, Longden, Thomas A., Laprade, Kathryn A., Stafford, James M., Ziemens, Dorothea, Schwaninger, Markus, Wenzel, Jan, Postnov, Dmitry D., Harraz, Osama F. |
| Předmět: |
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| Zdroj: |
Nature Communications; 10/7/2024, Vol. 15 Issue 1, p1-16, 16p |
| Abstrakt: |
Hyperemia in response to neural activity is essential for brain health. A hyperemic response delivers O2 and nutrients, clears metabolic waste, and concomitantly exposes cerebrovascular endothelial cells to hemodynamic forces. While neurovascular research has primarily centered on the front end of hyperemia—neuronal activity-to-vascular response—the mechanical consequences of hyperemia have gone largely unexplored. Piezo1 is an endothelial mechanosensor that senses hyperemia-associated forces. Using genetic mouse models and pharmacologic approaches to manipulate endothelial Piezo1 function, we evaluated its role in blood flow control and whether it impacts cognition. We provide evidence of a built-in brake system that sculpts hyperemia, and specifically show that Piezo1 activation triggers a mechano-feedback system that promotes blood flow recovery to baseline. Further, genetic Piezo1 modification led to deficits in complementary memory tasks. Collectively, our findings establish a role for endothelial Piezo1 in cerebral blood flow regulation and a role in its behavioral sequelae. On-demand blood flow increases are essential for brain health, but how flow recovers is unclear. Here, the authors show that brain perfusion triggers vascular Piezo1-mediated mechano-feedback that promotes blood flow recovery to baseline levels. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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