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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 4

Free radicals contribute to glia limitans breakdown, inflammation, and cortical cell death following reinjury.

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Free radicals contribute to glia limitans breakdown, inflammation, and c...
(A) Representative xz maximally projected Z stacks (300 μm in depth) of SR101 leakage (white) applied transcranially through the skull (green) in vehicle reinjury and 10 mM GSH reinjury. Glia limitans depicted as red dashed line. Scale bar: 40 μm. (B) Quantification of SR101 leakage by MFI. (C) Representative xy (top) and xz (bottom) maximally projected Z stacks (180 μm in depth) show LysM-GFP+ myelomonocytic cells (green) and vasculature labeled with Evans blue (red) in reinjured LysMgfp/+ reporter mice treated with either vehicle (PBS) or glutathione (GSH). See corresponding Supplemental Video 3. Images are representative of 2 independent experiments with 1–2 mice per group. Scale bars: 40 μm (top, xy) and 40 μm (bottom, xz). (D) Quantification of total myelomonocytic cells in the meninges. (E) Quantification of total myelomonocytic cells in the parenchyma. (F) Representative xy maximally projected Z stacks (100 μm in depth) show PI-labeled dead cells (red) in vehicle- or GSH-treated reinjury mice. Scale bar: 200 μm. (G) Quantification of cell death by selecting only PI+DAPI+ cells. Bar graphs represent 2 (B and G) to 3 (D and E) independent, pooled experiments with 2–5 mice per group per experiment. Each symbol in B, D, E, and G depicts an individual mouse. (B and G) Data were normalized to average reinjury vehicle per experimental day. (D and E) Data represent raw myelomonocytic cell counts. All data in B, D, E, and G are displayed as the mean fold change ± SD with **P ≤ 0.01 and ***P ≤ 0.001 using 2-tailed Student’s t test.

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