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1 ) 13:00-13:10 13:10-13:40 in vivo 13:40 14: in vivo 14:10 14:50 Takahiro Takano ()University of Rochester Medical Center Cerebrovascular tone control by astrocytes in vivo 15:00-15:30 "" 15:30 16:00 16:00 16:30 16:40 17:10 17:10 17:40 () 17:40 18:10 D- 19:00-20:00 20:00-21:00 Takahiro TakanoUniversity of Rochester Medical Center In vivo in vitro () 21:00 310
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4 2 1 1 Ca2 09mm EYFP Cerebral blood flow is dynamically coupled to the regional neuronal activity, but the mechanism by which local microcirculation is controlled remains unclear. Astrocytes have tight association with neurons and their endfeet cover vasculature in brain. Recent studies suggest that astrocytes can change vessel tone, but observations in slice preparations have been contradictory. Here we show that cortical astrocytes in vivo possess a powerful mechanism for rapid vasodilation, using two-photon microscope to visualize perfusion in single vessel in exposed cortex of live animals. Cranial window was made at somatosensory cortex of adult mice and blood vessels were visualized by systemic injection of fluorescent dye conjugated with dextran. Concentration of calcium in astrocytic endfeet surrounding penetrating arteries was monitored after loading with the calcium indicator dye. To selectively stimulate astrocytic endfeet, we triggered calcium increases by photolysis of DMNP-EDTA AM. UV photolysis resulted in rapid increase of calcium in astrocytic endfeet and arterial dilation. Vasodilation occurred with a latency of only 1-2 seconds. The effect is limited to arteries, and stimulating astrocytic Ca2+ signaling in vascular endfeet surrounding veins or capillaries did not trigger the changes in vessel diameters. Inhibiting cyclooxygenase-1 activity by either indomethacin or SC-560 blocked the photolysis-induced hyperemia, while antagonists of other vasomodulators failed to influence it. These observations implicate that astrocytes is in control of local microcirculation, and suggest that one of their physiological roles is to mediate vasodilation in response to increased neural activity. exo uteroenhanced yellow fluorescent protein in vivo
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