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Glia limitans superficialis oxidation and breakdown promote cortical cell death after repetitive head injury
Hannah D. Mason, … , Panagiotis Mastorakos, Dorian B. McGavern
Hannah D. Mason, … , Panagiotis Mastorakos, Dorian B. McGavern
Published August 24, 2021
Citation Information: JCI Insight. 2021;6(19):e149229. https://doi.org/10.1172/jci.insight.149229.
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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 1

Reinjury promotes degradation of the glia limitans superficialis.

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Reinjury promotes degradation of the glia limitans superficialis.
(A) Re...
(A) Representative xy maximally projected Z stacks (40 μm in depth) show ALDH1+ astrocytes (green) in Aldh1CreER/+ Stopfl/fl TdTomato naive, single-injury, and reinjury mice. All injury mice were sacrificed at 30 hours after initial mTBI. White dotted lines denote the vasculature. Images are representative of 4 independent mice per group. Scale bar: 20 μm. (B) Representative xz maximally projected Z stacks (300 μm in depth) of SR101 leakage (white) applied transcranially through the skull (green). Glia limitans superficialis depicted as red-dashed line. Scale bar: 20 μm. (C) Quantification of SR101 leakage by mean fluorescent intensity (MFI). (D) Representative xy maximal projection Z stacks (100 μm in depth) shows propidium iodide–labeled (PI-labeled) dead cells (red). Scale bar: 100 μm. (E) Quantification of cell death by selecting only PI+DAPI+ cells. Each symbol in C and E depicts an individual mouse. Bar graphs represent 2 independent pooled experiments with 3–5 mice per group per experiment. Data were normalized to average single injury mouse per experimental day and displayed as the mean fold change ± SD with *P ≤ 0.05 and ***P ≤ 0.001 (2-tailed Student’s t test).

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