Heterogeneity of Sensory-Induced Astrocytic Ca(2+) Dynamics During Functional Hyperemia

Astrocytic Ca(2+) fluctuations associated with functional hyperemia have typically been measured from large cellular compartments such as the soma, the whole arbor and the endfoot. The most prominent Ca(2+) event is a large magnitude, delayed signal that follows vasodilation. However, previous work has provided little information about the spatio-temporal properties of such Ca(2+) transients or their heterogeneity. Here, using an awake, in vivo two-photon fluorescence-imaging model, we performed detailed profiling of delayed astrocytic Ca(2+) signals across astrocytes or within individual astrocyte compartments using small regions of interest next to penetrating arterioles and capillaries along with vasomotor responses to vibrissae stimulation. We demonstrated that while a 5-s air puff that stimulates all whiskers predominantly generated reproducible functional hyperemia in the presence or absence of astrocytic Ca(2+) changes, whisker stimulation inconsistently produced astrocytic Ca(2+) responses. More importantly, these Ca(2+) responses were heterogeneous among subcellular structures of the astrocyte and across different astrocytes that resided within the same field of view. Furthermore, we found that whisker stimulation induced discrete Ca(2+) “hot spots” that spread regionally within the endfoot. These data reveal that astrocytic Ca(2+) dynamics associated with the microvasculature are more complex than previously thought, and highlight the importance of considering the heterogeneity of astrocytic Ca(2+) activity to fully understanding neurovascular coupling.