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Tieu, T.

Publications and source records attributed to Tieu, T..

2 recordsLinked to original sources
bioRxiv2024

Physiological and injury-induced microglial dynamics across the lifespan

Microglia are brains resident immune cells known for their dynamic responses to tissue and vascular injury. Little is known about how microglial activity differs across the life-stages of early development, adulthood, and aging. Using two-photon live imaging, we show that microglia in the adult cerebral cortex exhibit highly ramified processes and relatively immobile somata under basal conditions. Their responses to injury occur over minutes and are highly coordinated neighboring microglia. In neonates, microglia are denser and more mobile but less morphologically complex. Their responses to focal laser-induced injuries of capillaries or parenchymal tissue are uncoordinated, delayed and persistent over days. In the aged brain, microglia somata remain immobile under basal conditions but their processes become less ramified. Their responses to focal injuries remain coordinated but are slower and less sensitive. These studies confirm that microglia undergo significant changes in their morphology, distribution, dynamics and response to injury across the lifespan. HIGHLIGHTSO_LIMicroglia undergo significant morphological and dynamic changes between life-stages. C_LIO_LINeonatal microglia are highly dynamic, less morphologically complex and mount delayed responses to focal injury compared to adult microglia. C_LIO_LIAged microglia are slightly less ramified and their responses to focal injury are slow and less sensitive than adult microglial. C_LIO_LIMaturation of microglial morphology in the developing cortex is disrupted by focal laser injury. C_LI O_FIG O_LINKSMALLFIG WIDTH=163 HEIGHT=200 SRC="FIGDIR/small/615212v1_ufig1.gif" ALT="Figure 1"> View larger version (47K): org.highwire.dtl.DTLVardef@1ba9011org.highwire.dtl.DTLVardef@1485428org.highwire.dtl.DTLVardef@18d1f2aorg.highwire.dtl.DTLVardef@1f9086d_HPS_FORMAT_FIGEXP M_FIG C_FIG

neuroscience↗
bioRxiv2020

Brain capillary pericytes exert a substantial but slow influence on blood flow

The majority of the brains vasculature is comprised of intricate capillary networks lined by capillary pericytes. However, it remains unclear whether capillary pericytes contribute to blood flow control. Using two-photon microscopy to observe and manipulate single capillary pericytes in vivo, we find their optogenetic stimulation decreases lumen diameter and blood flow, but with slower kinetics than mural cells of upstream pial and pre-capillary arterioles. This slow, optogenetically-induced vasoconstriction was inhibited by the clinically-used vasodilator fasudil, a Rho kinase inhibitor that blocks contractile machinery. Capillary pericytes were also slower to constrict back to baseline following hypercapnia-induced dilation, and relax towards baseline following optogenetically-induced vasoconstriction. In a complementary approach, optical ablation of single capillary pericytes led to sustained local dilation and a doubling of blood cell flux in capillaries lacking pericyte contact. Altogether these data indicate that capillary pericytes contribute to basal blood flow resistance and slow modulation of blood flow throughout the capillary bed.

neuroscience↗