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Related Experiment Video

Updated: Dec 14, 2025

Reliable Isolation of Central Nervous System Microvessels Across Five Vertebrate Groups
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Transcriptomic comparison of human and mouse brain microvessels.

Hannah W Song1,2, Koji L Foreman1, Benjamin D Gastfriend1

  • 1Department of Chemical and Biological Engineering, University of Wisconsin-Madison, 1415 Engineering Dr., Madison, WI, 53706, USA.

Scientific Reports
|July 25, 2020
PubMed
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Researchers characterized the molecular makeup of brain microvessels in humans and mice. This work enhances understanding of the blood-brain barrier (BBB) and aids in developing new brain drug delivery strategies.

Area of Science:

  • Neuroscience
  • Vascular Biology
  • Genomics

Background:

  • The brain vasculature, specifically the blood-brain barrier (BBB), is crucial for maintaining brain homeostasis.
  • BBB dysfunction is implicated in various neurological disorders.
  • The molecular profiles of human brain microvascular endothelial cells (BMECs) and pericytes are not fully understood, hindering therapeutic development.

Purpose of the Study:

  • To comprehensively characterize the molecular constituents of human and mouse brain microvessels.
  • To identify novel genes and cell markers associated with brain endothelial cells and pericytes.
  • To explore species-specific gene expression differences relevant to BBB function and drug delivery.

Main Methods:

  • Laser capture microdissection (LCM) was used to isolate brain microvessels from human and mouse tissues.

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Last Updated: Dec 14, 2025

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  • RNA sequencing was performed on the isolated microvessel preparations to generate transcriptome datasets.
  • Bioinformatic analysis was employed to identify microvessel-enriched genes and compare human and mouse expression profiles.
  • Main Results:

    • Transcriptome data confirmed enrichment of known BMEC and pericyte markers.
    • Novel microvessel-enriched genes were identified.
    • Significant mouse-human differences in microvessel gene expression were discovered, with implications for BBB regulation and drug delivery.
    • Putative novel markers for human brain pericytes were identified by comparing LCM data with existing transcriptomic datasets.

    Conclusions:

    • This study provides an improved molecular definition of human and mouse BMECs and brain pericytes.
    • The generated datasets serve as a valuable resource for understanding brain vascular function and dysfunction.
    • These findings support the rational design of brain-penetrant therapeutics and strategies to overcome BBB challenges.