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RESEARCH PAPER / 2025-03-11

Impaired capillary-venous drainage contributes to gliosis and demyelination in white matter during aging

Stamenkovic, S., Schmid, F., Gurler, G., Abolmaali, F., Weitermann, N., Takasaki, K. T., Bonney, S. K., Sosa, M. J., Bennett, H. C., Kim, Y., Waters, J., Shih, A.

Seattle Children\\\'s Research Institute · biorxiv

Abstract

The progressive loss of cerebral white matter during aging contributes to cognitive decline, but whether reduced blood flow is a cause or consequence remains debated. Using deep multi-photon imaging in mice, we examined microvascular networks perfusing myelinated tissues in cortical layer 6 and corpus callosum. We identified sparse, wide-reaching venules, termed principal cortical venules, that exclusively drain deep tissues and resemble vasculature at the human cortex and U-fiber interface. Aging involved selective constriction and rarefaction of capillaries in deep branches of principal cortical venules. This resulted in mild hypoperfusion that was associated with microgliosis, astrogliosis and demyelination in deep tissues, but not upper cortex. Inducing a comparable hypoperfusion in adult mice using carotid artery stenosis triggered a similar tissue pathology specific to layer 6 and corpus callosum. Thus, impaired capillary-venous drainage is a contributor to hypoperfusion and a potential therapeutic target for preserving blood flow to white matter during aging.

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Research summary

Impaired capillary-venous drainage contributes to hypoperfusion and subsequent gliosis and demyelination in aging white matter. The study addresses a potential root cause of cognitive decline associated with aging, focusing on microvascular changes that could inform therapeutic strategies for age-related cognitive decline.

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