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Marker Reveals Pericyte Specification in the Mouse Central Nervous System

Overview
Journal J Neurosci
Specialty Neurology
Date 2024 Sep 11
PMID 39261008
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Abstract

Perivascular mural cells including vascular smooth cells (VSMCs) and pericytes are integral components of the vascular system. In the central nervous system (CNS), pericytes are also indispensable for the blood-brain barrier (BBB), blood-spinal cord barrier, and blood-retinal barrier and play key roles in maintaining cerebrovascular and neuronal functions. However, the functional specifications of pericytes between CNS and peripheral organs have not been resolved at the genetic and molecular levels. Hence, the generation of reliable CNS pericyte-specific models and genetic tools remains very challenging. Here, we report a new CNS pericyte marker in mice. This putative cation-transporting ATPase 13A5 () marker was identified through single-cell transcriptomics, based on its specificity to brain pericytes. We further generated a knock-in model with both tdTomato reporter and Cre recombinase. Using this model to trace the distribution of positive pericytes in mice, we found that the tdTomato reporter reliably labels the CNS pericytes, including the ones in spinal cord and retina but not peripheral organs. Interestingly, brain pericytes are likely shaped by the developing neural environment, as positive pericytes start to appear around murine embryonic day 15 (E15) and expand along the cerebrovasculature. Thus, is a specific marker of CNS pericyte lineage, and this based model is a reliable tool to explore the heterogeneity of pericytes and BBB functions in health and diseases.

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References
1.
Daneman R, Zhou L, Agalliu D, Cahoy J, Kaushal A, Barres B . The mouse blood-brain barrier transcriptome: a new resource for understanding the development and function of brain endothelial cells. PLoS One. 2010; 5(10):e13741. PMC: 2966423. DOI: 10.1371/journal.pone.0013741. View

2.
Saunders A, Macosko E, Wysoker A, Goldman M, Krienen F, de Rivera H . Molecular Diversity and Specializations among the Cells of the Adult Mouse Brain. Cell. 2018; 174(4):1015-1030.e16. PMC: 6447408. DOI: 10.1016/j.cell.2018.07.028. View

3.
Gerl K, Miquerol L, Todorov V, Hugo C, Adams R, Kurtz A . Inducible glomerular erythropoietin production in the adult kidney. Kidney Int. 2015; 88(6):1345-1355. DOI: 10.1038/ki.2015.274. View

4.
Ximerakis M, Lipnick S, Innes B, Simmons S, Adiconis X, Dionne D . Single-cell transcriptomic profiling of the aging mouse brain. Nat Neurosci. 2019; 22(10):1696-1708. DOI: 10.1038/s41593-019-0491-3. View

5.
Sheikh B, Guhathakurta S, Tsang T, Schwabenland M, Renschler G, Herquel B . Neural metabolic imbalance induced by MOF dysfunction triggers pericyte activation and breakdown of vasculature. Nat Cell Biol. 2020; 22(7):828-841. DOI: 10.1038/s41556-020-0526-8. View