Atp13a5 Marker Reveals Pericytes of The Central Nervous System in Mice
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 known as the guardian of the blood-brain barrier, blood-spinal cord barrier and blood-retinal barrier, and play key roles in maintaining cerebrovascular and neuronal functions. However, the functional difference between CNS and peripheral pericytes has 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 cation-transporting ATPase 13A5 (Atp13a5) marker is highly specific to the pericytes in brain, spinal cord and retina. We generated a transgenic model with a knock-in tdTomato reporter and Cre recombinase. The tdTomato reporter reliably labels the CNS pericytes, but not found in any other CNS cell types including closely related VSMCs, or in peripheral organs. More importantly, Atp13a5 is turned on at embryonic day E15, suggesting brain pericytes are shaped by the developing neural environment. We hope that the new tools will allow us to further explore the heterogeneity of pericytes and achieve a better understanding of CNS pericytes in health and diseases.
Additional Information
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. This version posted July 10, 2021. The work of Z.Z. is supported by the National Institutes of Health (NIH) grant nos. R01AG061288, R01NS110687 and RF1NS122060, and BrightFocus Foundation grant no. A2019218S. Author contributions: XG and ZZ designed and performed experiments and analyzed data and wrote the manuscript. TG, SX, HW, MC, XX, BZ and FG performed experiments and/or analyzed data. JZ, JFC, DZ, AM and FG contributed to writing the manuscript. All authors read and approved the final manuscript. The authors have declared no competing interest.Attached Files
Submitted - 2021.07.09.451694v1.full.pdf
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Additional details
- Eprint ID
- 109939
- Resolver ID
- CaltechAUTHORS:20210720-203604788
- NIH
- R01AG061288
- NIH
- R01NS110687
- NIH
- RF1NS122060
- BrightFocus Foundation
- A2019218S
- Created
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2021-07-21Created from EPrint's datestamp field
- Updated
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2021-11-16Created from EPrint's last_modified field