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Keeping the Brain Well Fed: The Role of Capillaries and Arterioles in Orchestrating Functional Hyperemia

2018; Cell Press; Volume: 99; Issue: 2 Linguagem: Inglês

10.1016/j.neuron.2018.07.011

1097-4199

Amy R. Nippert, Anusha Mishra, Eric A. Newman,

Traumatic Brain Injury and Neurovascular Disturbances

Cerebral blood flow increases in regions of increased brain activity. In this issue of Neuron, Rungta et al., 2018Rungta R.L. Chaigneau E. Osmanski B.F. Charpak S. Vascular compartmentalization of functional hyperemia from the synapse to the pia.Neuron. 2018; 99 (this issue): 362-375Abstract Full Text Full Text PDF PubMed Scopus (123) Google Scholar characterize the contribution of different vascular compartments in generating this increase and outline the time course of arteriole and capillary dilation in generating functional hyperemia. Cerebral blood flow increases in regions of increased brain activity. In this issue of Neuron, Rungta et al., 2018Rungta R.L. Chaigneau E. Osmanski B.F. Charpak S. Vascular compartmentalization of functional hyperemia from the synapse to the pia.Neuron. 2018; 99 (this issue): 362-375Abstract Full Text Full Text PDF PubMed Scopus (123) Google Scholar characterize the contribution of different vascular compartments in generating this increase and outline the time course of arteriole and capillary dilation in generating functional hyperemia. The brain is a hungry organ, consuming 20% to 25% of the total oxygen and glucose utilized by the body. Many mechanisms have evolved to ensure that the brain receives adequate nourishment to maintain its health and proper function. When a region of the brain is active, blood flow to that region increases via a process termed functional hyperemia, bringing additional nutrients to the active neurons and removing metabolic byproducts. This coupling between neuronal activity and blood flow allows imaging techniques, such as blood-oxygen-level-dependent functional magnetic resonance imaging (BOLD fMRI), which use the functional hyperemia response to determine regions of brain activity based on changes in blood flow and oxygenation. Fundamental questions about the nature of functional hyperemia remain unsolved, complicating interpretation of fMRI. One such question concerns whether capillaries, as well as arterioles, actively dilate in response to neuronal activity (Nippert et al., 2018Nippert A.R. Biesecker K.R. Newman E.A. Mechanisms mediating functional hyperemia in the brain.Neuroscientist. 2018; 24: 73-83Crossref PubMed Scopus (68) Google Scholar). The question is critical, as it determines whether blood flow increases can be targeted precisely to regions of activity and defines the limits of spatial resolution achievable by BOLD imaging. Traditionally, it was believed that increases in blood flow were regulated entirely by arteries and arterioles on the pial surface of the brain and penetrating arterioles within the brain parenchyma. Recently, however, several laboratories have reported that capillaries also dilate actively following neuronal activation and contribute to functional hyperemia (Hall et al., 2014Hall C.N. Reynell C. Gesslein B. Hamilton N.B. Mishra A. Sutherland B.A. O'Farrell F.M. Buchan A.M. Lauritzen M. Attwell D. Capillary pericytes regulate cerebral blood flow in health and disease.Nature. 2014; 508: 55-60Crossref PubMed Scopus (1113) Google Scholar, Kornfield and Newman, 2014Kornfield T.E. Newman E.A. Regulation of blood flow in the retinal trilaminar vascular network.J. Neurosci. 2014; 34: 11504-11513Crossref PubMed Scopus (128) Google Scholar, Tian et al., 2010Tian P. Teng I.C. May L.D. Kurz R. Lu K. Scadeng M. Hillman E.M. De Crespigny A.J. D'Arceuil H.E. Mandeville J.B. et al.Cortical depth-specific microvascular dilation underlies laminar differences in blood oxygenation level-dependent functional MRI signal.Proc. Natl. Acad. Sci. USA. 2010; 107: 15246-15251Crossref PubMed Scopus (220) Google Scholar). This observation is controversial, as one report claims that pericytes, the vascular mural cells that surround capillaries and are analogous to arteriolar smooth muscle cells (SMCs), do not express contractile proteins (Hill et al., 2015Hill R.A. Tong L. Yuan P. Murikinati S. Gupta S. Grutzendler J. Regional blood flow in the normal and ischemic brain Is controlled by arteriolar smooth muscle cell contractility and not by capillary pericytes.Neuron. 2015; 87: 95-110Abstract Full Text Full Text PDF PubMed Scopus (418) Google Scholar). A recent publication (Alarcon-Martinez et al., 2018Alarcon-Martinez L. Yilmaz-Ozcan S. Yemisci M. Schallek J. Kılıç K. Can A. Di Polo A. Dalkara T. Capillary pericytes express α-smooth muscle actin, which requires prevention of filamentous-actin depolymerization for detection.eLife. 2018; 7: e34861Crossref PubMed Scopus (130) Google Scholar) has demonstrated, however, that pericytes express alpha-smooth muscle actin and can constrict and relax. Furthermore, pericytes may also express actin isomers other than alpha-smooth muscle actin (DeNofrio et al., 1989DeNofrio D. Hoock T.C. Herman I.M. Functional sorting of actin isoforms in microvascular pericytes.J. Cell Biol. 1989; 109: 191-202Crossref PubMed Scopus (114) Google Scholar). In this issue of Neuron, Rungta et al., 2018Rungta R.L. Chaigneau E. Osmanski B.F. Charpak S. Vascular compartmentalization of functional hyperemia from the synapse to the pia.Neuron. 2018; 99 (this issue): 362-375Abstract Full Text Full Text PDF PubMed Scopus (123) Google Scholar make a major contribution to resolving the problem of which vessels generate functional hyperemia. Working in the mouse olfactory bulb in vivo, they demonstrate that capillaries, as well as arterioles, actively dilate in response to neuronal activity and contribute substantially to functional hyperemia. In this elegant study, Rungta et al., 2018Rungta R.L. Chaigneau E. Osmanski B.F. Charpak S. Vascular compartmentalization of functional hyperemia from the synapse to the pia.Neuron. 2018; 99 (this issue): 362-375Abstract Full Text Full Text PDF PubMed Scopus (123) Google Scholar use a variety of imaging techniques to simultaneously monitor several aspects of functional hyperemia. Using two-photon microscopy, they monitor activation of neuronal terminals by imaging Ca2+ signals in oligodendrocyte precursor cells, which they demonstrate faithfully follow presynaptic activity. They then monitor vascular responses by imaging Ca2+ within SMCs surrounding arterioles and within pericytes surrounding capillaries, an innovative and powerful method, as these Ca2+ responses occur faster than the dilation of vessels and show individual mural cell activation state independent of changes in vessel diameter or blood velocity. They simultaneously monitor vessel diameter and blood velocity with two-photon line scans. Rungta et al., 2018Rungta R.L. Chaigneau E. Osmanski B.F. Charpak S. Vascular compartmentalization of functional hyperemia from the synapse to the pia.Neuron. 2018; 99 (this issue): 362-375Abstract Full Text Full Text PDF PubMed Scopus (123) Google Scholar divide the vasculature into four functional units (see Figure 1): (1) pial arterioles, (2) parenchymal arterioles and the first-order capillaries branching from them, which they define as the primary functional unit, (3) the downstream, higher-order capillaries (the secondary functional unit), and (4) the smallest, highest-order capillaries, which are juxtaposed to the olfactory nerve terminals. They find that olfactory stimuli induce a decrease in intracellular Ca2+ in pericytes and SMCs throughout the vascular tree and that this decrease in Ca2+ occurs fastest and synchronously in the first three functional compartments compared to the fourth juxta-synaptic compartment. Yet, there is a difference in the evoked dilation of the vessels: the arterioles and capillaries of the primary functional unit dilate first while the pial arterioles and capillaries of the secondary functional unit dilate more slowly. The smallest juxta-synaptic capillaries (those 5 to 8 branches from parenchymal arterioles) do not actively dilate to olfactory stimuli despite the decrease in Ca2+ observed in the thin-strand pericytes contacting them. Rather, they dilate passively due to an increase in upstream perfusion pressure. Counterintuitively, while the primary functional unit dilates fastest, increases in blood velocity are fastest and largest in the smallest capillaries. The persuasiveness of Rungta et al., 2018Rungta R.L. Chaigneau E. Osmanski B.F. Charpak S. Vascular compartmentalization of functional hyperemia from the synapse to the pia.Neuron. 2018; 99 (this issue): 362-375Abstract Full Text Full Text PDF PubMed Scopus (123) Google Scholar's findings is buttressed by an associated modeling study, which simulates the experimental results. The model predicts blood flow changes in response to experimentally measured changes in vessel diameter in the four vascular compartments. As observed experimentally, the simulations demonstrate that blood velocity increases should be delayed in the primary functional unit because of the large volume increase in that compartment produced by vessel dilation. The same effect accounts for the transient decrease in blood velocity sometimes seen in this compartment. The simulations also indicate that the largest blood velocity increases should occur in the smallest capillaries, which only dilate passively. Additional important insights are derived from the modeling study. The simulations indicate that active dilation of capillaries in the secondary functional unit contribute to blood flow increases. More surprisingly, the smallest, highest-order capillaries also contribute substantially to functional hyperemia. When the passive dilation of these capillaries is removed from the simulation, the blood flow increase is reduced by almost half. This finding is in line with previous studies indicating that a large fraction of the total vascular resistance in the brain resides within the capillary network (Blinder et al., 2013Blinder P. Tsai P.S. Kaufhold J.P. Knutsen P.M. Suhl H. Kleinfeld D. The cortical angiome: an interconnected vascular network with noncolumnar patterns of blood flow.Nat. Neurosci. 2013; 16: 889-897Crossref PubMed Scopus (355) Google Scholar). The observation that these capillaries do not actively dilate but that pericytes around them nonetheless display Ca2+ decreases suggests that Ca2+ in these pericytes may contribute to the stiffness of the capillary wall. The work of Rungta et al., 2018Rungta R.L. Chaigneau E. Osmanski B.F. Charpak S. Vascular compartmentalization of functional hyperemia from the synapse to the pia.Neuron. 2018; 99 (this issue): 362-375Abstract Full Text Full Text PDF PubMed Scopus (123) Google Scholar raises important additional questions. The smallest high-order capillaries are closest to the synaptic terminals activated by olfactory stimuli. Yet, the pericytes associated with these capillaries respond more slowly than pericytes and SMCs associated with upstream vessels of the primary functional unit. Why do the contractile cells farther from the site of neural activity respond faster? Rungta et al., 2018Rungta R.L. Chaigneau E. Osmanski B.F. Charpak S. Vascular compartmentalization of functional hyperemia from the synapse to the pia.Neuron. 2018; 99 (this issue): 362-375Abstract Full Text Full Text PDF PubMed Scopus (123) Google Scholar suggest that a vasodilating signal (cell hyperpolarization) is propagated rapidly upstream through the vascular endothelial cells. This supports the idea that endothelial cells, rather than pericytes and SMCs, detect neuronal activity, as suggested previously (Chen et al., 2014Chen B.R. Kozberg M.G. Bouchard M.B. Shaik M.A. Hillman E.M. A critical role for the vascular endothelium in functional neurovascular coupling in the brain.J. Am. Heart Assoc. 2014; 3: e000787Crossref PubMed Scopus (218) Google Scholar). However, this still does not explain why pericytes surrounding the smallest capillaries respond more slowly. Perhaps, as Rungta et al., 2018Rungta R.L. Chaigneau E. Osmanski B.F. Charpak S. Vascular compartmentalization of functional hyperemia from the synapse to the pia.Neuron. 2018; 99 (this issue): 362-375Abstract Full Text Full Text PDF PubMed Scopus (123) Google Scholar suggest, these pericytes are less closely coupled to the endothelial cells than are the upstream pericytes. Or perhaps the molecular machinery generating the Ca2+ decreases in these pericytes is weaker or slower. Further, these data do not exclude the possibility that the juxta-synaptic pericytes hyperpolarize first in response to neuronal activity and transmit this signal to the endothelial cells. The question of whether endothelial cells, pericytes, or SMCs are the first responders in functional hyperemia can only be determined by future experiments comparing the time course of hyperpolarization of each cell type. Other questions arise from the work of Rungta et al., 2018Rungta R.L. Chaigneau E. Osmanski B.F. Charpak S. Vascular compartmentalization of functional hyperemia from the synapse to the pia.Neuron. 2018; 99 (this issue): 362-375Abstract Full Text Full Text PDF PubMed Scopus (123) Google Scholar. Is blood flow regulated by the same vascular compartments in other brain regions as in the olfactory bulb? One study in the rodent barrel cortex indicates that first-order capillaries dilate before the penetrating (parenchymal) arterioles (Hall et al., 2014Hall C.N. Reynell C. Gesslein B. Hamilton N.B. Mishra A. Sutherland B.A. O'Farrell F.M. Buchan A.M. Lauritzen M. Attwell D. Capillary pericytes regulate cerebral blood flow in health and disease.Nature. 2014; 508: 55-60Crossref PubMed Scopus (1113) Google Scholar), while another study in the somatosensory cortex shows that penetrating arterioles dilate slightly before first-order capillaries (Tian et al., 2010Tian P. Teng I.C. May L.D. Kurz R. Lu K. Scadeng M. Hillman E.M. De Crespigny A.J. D'Arceuil H.E. Mandeville J.B. et al.Cortical depth-specific microvascular dilation underlies laminar differences in blood oxygenation level-dependent functional MRI signal.Proc. Natl. Acad. Sci. USA. 2010; 107: 15246-15251Crossref PubMed Scopus (220) Google Scholar). By comparison, Rungta et al., 2018Rungta R.L. Chaigneau E. Osmanski B.F. Charpak S. Vascular compartmentalization of functional hyperemia from the synapse to the pia.Neuron. 2018; 99 (this issue): 362-375Abstract Full Text Full Text PDF PubMed Scopus (123) Google Scholar observe near-simultaneous contractile cell Ca2+ decreases and vessel dilation in the capillaries and arterioles of the primary functional unit. Some of these discrepancies may be explained by differences in layer-specific vascular responsiveness in different cortical regions (Tian et al., 2010Tian P. Teng I.C. May L.D. Kurz R. Lu K. Scadeng M. Hillman E.M. De Crespigny A.J. D'Arceuil H.E. Mandeville J.B. et al.Cortical depth-specific microvascular dilation underlies laminar differences in blood oxygenation level-dependent functional MRI signal.Proc. Natl. Acad. Sci. USA. 2010; 107: 15246-15251Crossref PubMed Scopus (220) Google Scholar). In summary, Rungta et al., 2018Rungta R.L. Chaigneau E. Osmanski B.F. Charpak S. Vascular compartmentalization of functional hyperemia from the synapse to the pia.Neuron. 2018; 99 (this issue): 362-375Abstract Full Text Full Text PDF PubMed Scopus (123) Google Scholar make major contributions to our understanding of how blood flow is regulated in the brain. Their work is a technical tour de force, simultaneously monitoring neuronal activity, responses of pericytes and SMCs, vessel dilation, and blood velocity and further utilizing computational modeling to interpret their observations. This is an important advance over previous studies, which limited their scope to only a few of these responses. Using these imaging techniques, Rungta et al., 2018Rungta R.L. Chaigneau E. Osmanski B.F. Charpak S. Vascular compartmentalization of functional hyperemia from the synapse to the pia.Neuron. 2018; 99 (this issue): 362-375Abstract Full Text Full Text PDF PubMed Scopus (123) Google Scholar determine which vascular compartments generate functional hyperemia and characterize the dynamics of the responses in greater detail than previously possible. This study adds to an accumulating body of work demonstrating the importance of capillaries in generating functional hyperemia. Vascular Compartmentalization of Functional Hyperemia from the Synapse to the PiaRungta et al.NeuronJune 21, 2018In BriefRungta et al. perform in vivo two-photon calcium imaging of neuron, oligodendrocyte precursor cell, pericyte, and smooth muscle cell responses to olfactory sensory stimulation in combination with vessel diameter and red blood cell velocity measurements along the entire vascular arbor. 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