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Glia limitans superficialis oxidation and breakdown promote cortical cell death after repetitive head injury
Hannah D. Mason, Alexis M. Johnson, Nicole A. Mihelson, Panagiotis Mastorakos, Dorian B. McGavern
Hannah D. Mason, Alexis M. Johnson, Nicole A. Mihelson, Panagiotis Mastorakos, Dorian B. McGavern
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Research Article Immunology Neuroscience

Glia limitans superficialis oxidation and breakdown promote cortical cell death after repetitive head injury

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Abstract

Repetitive mild traumatic brain injuries (mTBI) disrupt CNS barriers, the erosion of which has been linked to long-term neurodegenerative and psychiatric conditions. Although much attention has been devoted to CNS vasculature following mTBI, little is known about the glia limitans superficialis — a barrier of surface-associated astrocytes that helps protect the CNS parenchyma and maintain homeostasis. Here, we identify the glia limitans superficialis as a crucial barrier surface whose breakdown after acute repeat mTBI facilitates increased cell death and recruitment of peripheral myelomonocytic cells. Using intravital microscopy, we show that brain-resident microglia fortify this structure after a single mTBI, yet they fail to do so following secondary injury, which triggers massive recruitment of myelomonocytic cells from the periphery that contribute to further destruction of the glia limitans superficialis but not cortical cell death. We demonstrate, instead, that reactive oxygen species (ROS) generated in response to repetitive head injury are largely responsible for enhanced cortical cell death, and therapeutic administration of the antioxidant glutathione markedly reduces this cell death, preserves the glia limitans, and prevents myelomonocytic cells from entering the brain parenchyma. Collectively, our findings underscore the importance of preserving the glia limitans superficialis after brain injury and offer a therapeutic means to protect this structure and the underlying cortex.

Authors

Hannah D. Mason, Alexis M. Johnson, Nicole A. Mihelson, Panagiotis Mastorakos, Dorian B. McGavern

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Figure 2

Reinjury promotes loss of microglia.

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Reinjury promotes loss of microglia.
(A) Representative xy (top) and xz ...
(A) Representative xy (top) and xz (bottom) maximally projected Z stacks (180 μm in depth) show CX3CR1gfp/+ myeloid cells (green) and vasculature labeled with Evans blue (red) in Cx3cr1gfp/+ reporter mice without injury, with single injury, or with reinjury. See corresponding Supplemental Video 1. Images are representative of 4 independent mice per group. Scale bar: 20 μm (top, xy) and 20μm (bottom, xz). (B) Concatenated UMAPS generated from high-dimensional flow cytometric analysis (gating shown in Supplemental Figure 1A) of 2 mm cortical punch biopsies from the above groups show 4 different subsets of microglia identified as populations 1 (blue), 2 (green), 3 (pink), and 4 (orange). Dots depict cellularity. (C) Histograms show the relative expression of FSC-area (FSC-A), SSC-A, CD45, CD11b, CX3CR1, F480, P2RY12, CD206, and CD44 on composite, concatenated microglia populations 1 (blue), 2 (green), 3 (pink), and 4 (orange). (D) Quantification of microglia total per experimental group. (E) Quantification of the frequency of each microglia subtype per experimental group. Each symbol in D and E depicts an individual mouse. Bar graphs are representative of 2 independent experiments with 4–5 mice per experimental group. Data are displayed as mean ± SD with *P≤ 0.05, **P ≤ 0.01, and ***P ≤ 0.001 using 1-way ANOVA with Fisher’s LSD test (D) and multiple t tests with Holm-Sidak multiple comparisons test (E).

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