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Updated: May 29, 2025

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A High Output Method to Isolate Cerebral Pericytes from Mouse
Published on: January 14, 2020
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Screening and Identification of Brain Pericyte-Selective Markers.
Minkyung Kang1, Ava Nasrollahi1, Feng Cheng2
1Department of Molecular Pharmacology and Physiology, Morsani College of Medicine, University of South Florida, Tampa, Florida, USA.
CNS Neuroscience & Therapeutics
|February 6, 2025
Summary
Researchers identified new brain pericyte markers, Pla1a and Cox4i2. These genes help distinguish pericyte subpopulations from vascular smooth muscle cells, advancing central nervous system research.
Area of Science:
- Neuroscience
- Cell Biology
- Genomics
Background:
- Pericytes are crucial mural cells in the central nervous system (CNS).
- A significant challenge in pericyte research is the absence of specific markers for pericytes and their subpopulations.
- Identifying these markers is vital for understanding pericyte function and heterogeneity in the CNS.
Purpose of the Study:
- To identify novel genes specifically enriched in brain pericytes.
- To find markers that can differentiate pericyte subpopulations from vascular smooth muscle cells (vSMCs).
- To facilitate further research into the distinct roles of pericyte subpopulations in the CNS.
Main Methods:
- Generation of a novel transgenic mouse line with permanent tdTomato labeling of vSMCs.
- Isolation of PDGFRβ+tdTomato- pericytes and PDGFRβ+tdTomato+ vSMCs from mouse brains.
- RNA sequencing (RNAseq) analysis to identify pericyte- and vSMC-enriched genes.
Main Results:
- Identification of 40 pericyte-enriched genes and 158 vSMC-enriched genes.
- Discovery that Pla1a and Cox4i2 are predominantly enriched in subpopulations of brain pericytes.
- Observation that Pla1a and Cox4i2 also mark some non-vascular parenchymal cells, indicating potential broader applications.
Conclusions:
- Pla1a and Cox4i2 show preferential enrichment in brain pericyte subpopulations over vSMCs.
- These genes serve as valuable tools for distinguishing pericyte subpopulations in the brain.
- The findings contribute to a better understanding of pericyte heterogeneity and function in the CNS.

