4.7 Article

Glial Cell Calcium Signaling Mediates Capillary Regulation of Blood Flow in the Retina

Journal

JOURNAL OF NEUROSCIENCE
Volume 36, Issue 36, Pages 9435-9445

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.1782-16.2016

Keywords

blood flow; calcium signaling; capillary; glia; neurovascular coupling; retina

Categories

Funding

  1. NIH [R01-EY04077, P30-EY11374, P50-MH084020, P30-NS050274]
  2. MinnCReST Predoctoral Training Fellowship [T90 DE 022732]
  3. NIH Predoctoral Training of Neuroscientists Grant [T32GM0D8471]

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The brain is critically dependent on the regulation of blood flow to nourish active neurons. One widely held hypothesis of blood flow regulation holds that active neurons stimulate Ca2+ increases in glial cells, triggering glial release of vasodilating agents. This hypothesis has been challenged, as arteriole dilation can occur in the absence of glial Ca2+ signaling. We address this controversy by imaging glial Ca2+ signaling and vessel dilation in the mouse retina. We find that sensory stimulation results in Ca2+ increases in the glial endfeet contacting capillaries, but not arterioles, and that capillary dilations often follow spontaneous Ca2+ signaling. In IP3R2(-/-) mice, where glial Ca2+ signaling is reduced, light-evoked capillary, but not arteriole, dilation is abolished. The results show that, independent of arterioles, capillaries actively dilate and regulate blood flow. Furthermore, the results demonstrate that glial Ca2+ signaling regulates capillary but not arteriole blood flow.

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