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Molecular anatomy of adult mouse leptomeninges

Authors :
Pietilä, Riikka
Del Gaudio, Francesca
He, Liqun
Vázquez-Liébanas, Elisa
Vanlandewijck, Michael
Muhl, Lars
Mocci, Giuseppe
Bjørnholm, Katrine D.
Lindblad, Caroline
Fletcher-Sandersjöö, Alexander
Svensson, Mikael
Thelin, Eric P.
Liu, Jianping
van Voorden, A. Jantine
Torres, Monica
Antila, Salli
Xin, Li
Karlström, Helena
Storm-Mathisen, Jon
Bergersen, Linda Hildegard
Moggio, Aldo
Hansson, Emil M.
Ulvmar, Maria H.
Nilsson, Per
Mäkinen, Taija
Andaloussi Mäe, Maarja
Alitalo, Kari
Proulx, Steven T.
Engelhardt, Britta
McDonald, Donald M.
Lendahl, Urban
Andrae, Johanna
Betsholtz, Christer
Pietilä, Riikka
Del Gaudio, Francesca
He, Liqun
Vázquez-Liébanas, Elisa
Vanlandewijck, Michael
Muhl, Lars
Mocci, Giuseppe
Bjørnholm, Katrine D.
Lindblad, Caroline
Fletcher-Sandersjöö, Alexander
Svensson, Mikael
Thelin, Eric P.
Liu, Jianping
van Voorden, A. Jantine
Torres, Monica
Antila, Salli
Xin, Li
Karlström, Helena
Storm-Mathisen, Jon
Bergersen, Linda Hildegard
Moggio, Aldo
Hansson, Emil M.
Ulvmar, Maria H.
Nilsson, Per
Mäkinen, Taija
Andaloussi Mäe, Maarja
Alitalo, Kari
Proulx, Steven T.
Engelhardt, Britta
McDonald, Donald M.
Lendahl, Urban
Andrae, Johanna
Betsholtz, Christer
Publication Year :
2023

Abstract

Leptomeninges, consisting of the pia mater and arachnoid, form a connective tissue investment and barrier enclosure of the brain. The exact nature of leptomeningeal cells has long been debated. In this study, we iden-tify five molecularly distinct fibroblast-like transcriptomes in cerebral leptomeninges; link them to anatomically distinct cell types of the pia, inner arachnoid, outer arachnoid barrier, and dural border layer; and contrast them to a sixth fibroblast-like transcriptome present in the choroid plexus and median eminence. Newly identified transcriptional markers enabled molecular characterization of cell types responsible for adherence of arach-noid layers to one another and for the arachnoid barrier. These markers also proved useful in identifying the molecular features of leptomeningeal development, injury, and repair that were preserved or changed after traumatic brain injury. Together, the findings highlight the value of identifying fibroblast transcriptional subsets and their cellular locations toward advancing the understanding of leptomeningeal physiology and pathology.<br />De fyra första författarna delar förstaförfattarskapetDe tre sista författarna delar sistaförfattarskapet

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1422607041
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1016.j.neuron.2023.09.002