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.

Highlights

  • Traumatic brain injuries (TBI) represent a dire global health and economic problem, impacting 69 million people worldwide and costing approximately $400 billion (USD) in associated medical fees annually [1, 2]

  • We initially examined the structural integrity of the glia limitans superficialis in Aldh1CreER/+ Stopfl/fl TdTomato mice fed tamoxifen chow for 3 weeks to induce expression of Aldh1 — a promoter active in most adult astrocytes [15]

  • Decades of research have been dedicated to understanding blood brain barrier (BBB) destruction following TBI, little is known about mechanisms that inflame and break down the glia limitans superficialis, despite its crucial role in protecting the CNS parenchyma

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Summary

Introduction

Traumatic brain injuries (TBI) represent a dire global health and economic problem, impacting 69 million people worldwide and costing approximately $400 billion (USD) in associated medical fees annually [1, 2]. The glia limitans superficialis is a layer of surface-associated astrocytes that resides beneath the pia mater and serves as a barrier between cerebral spinal fluid space and CNS parenchyma [12]. It covers the entire brain parenchyma, yet little is known about this important barrier surface in the context of TBI, despite the fact that it is permeabilized following brain injury [6, 13]. We set out to elucidate mechanisms of glia limitans superficialis breakdown after single and repetitive mTBI, with the hope of discovering a druggable pathway to preserve barrier integrity and mitigate adverse, postinjury outcomes

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