Shared inflammatory glial cell signature after stab wound injury, revealed by spatial, temporal, and cell-type-specific profiling of the murine cerebral cortex

• Published in: Nature communications Vol. 15; no. 1; p. 2866
• Main Authors: Koupourtidou, Christina, Schwarz, Veronika, Aliee, Hananeh, Frerich, Simon, Fischer-Sternjak, Judith, Bocchi, Riccardo, Simon-Ebert, Tatiana, Bai, Xianshu, Sirko, Swetlana, Kirchhoff, Frank, Dichgans, Martin, Götz, Magdalena, Theis, Fabian J., Ninkovic, Jovica
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 03.04.2024; Nature Publishing Group; Nature Portfolio
• Subjects: 13; 13/51; 38/39; 38/91; 631/378/1687; 631/378/2596; 631/378/87; Brain; Cerebral cortex; CXCR3 protein; Glial cells; Head injuries; Humanities and Social Sciences; Inflammation; Injury analysis; multidisciplinary; Neurodegenerative diseases; Neuroglia; Regeneration; Science; Science (multidisciplinary); Temporal lobe; TLR1 protein; Toll-like receptors; Transcriptomics; Traumatic brain injury
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-024-46625-w

Traumatic brain injury leads to a highly orchestrated immune- and glial cell response partially responsible for long-lasting disability and the development of secondary neurodegenerative diseases. A holistic understanding of the mechanisms controlling the responses of specific cell types and their crosstalk is required to develop an efficient strategy for better regeneration. Here, we combine spatial and single-cell transcriptomics to chart the transcriptomic signature of the injured male murine cerebral cortex, and identify specific states of different glial cells contributing to this signature. Interestingly, distinct glial cells share a large fraction of injury-regulated genes, including inflammatory programs downstream of the innate immune-associated pathways Cxcr3 and Tlr1/2. Systemic manipulation of these pathways decreases the reactivity state of glial cells associated with poor regeneration. The functional relevance of the discovered shared signature of glial cells highlights the importance of our resource enabling comprehensive analysis of early events after brain injury. Glial cells and their crosstalk after injury are crucial for brain regeneration. Here, the authors show the spatial, temporal, and single-cell responses of glial cells after injury and identify shared pathways controlling glial reactivity.