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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This study has established a stable and efficient method for the isolation, culture, and functional determination of vascular wall-resident CD34+ stem cells (CD34+ VW-SCs). This easy-to-follow and time-effective isolation method can be utilized by other investigators to study the potential mechanisms involved in cardiovascular diseases.

Abstract

Resident CD34+ vascular wall-resident stem and progenitor cells (VW-SCs) are increasingly recognized for their crucial role in regulating vascular injury and repair. Establishing a stable and efficient method to culture functional murine CD34+ VW-SCs is essential for further investigating the mechanisms involved in the proliferation, migration, and differentiation of these cells under various physiological and pathological conditions. The described method combines magnetic bead screening and flow cytometry to purify primary cultured resident CD34+ VW-SCs. The purified cells are then functionally identified through immunofluorescence staining and Ca2+ imaging. Briefly, vascular cells from the adventitia of the murine aorta and mesenteric artery are obtained through tissue block attachment, followed by subculturing until reaching a cell count of at least 1 × 107. Subsequently, CD34+ VW-SCs are purified using magnetic bead sorting and flow cytometry. Identification of CD34+ VW-SCs involves cellular immunofluorescence staining, while functional multipotency is determined by exposing cells to a specific culture medium for oriented differentiation. Moreover, functional internal Ca2+ release and external Ca2+ entry is assessed using a commercially available imaging workstation in Fura-2/AM-loaded cells exposed to ATP, caffeine, or thapsigargin (TG). This method offers a stable and efficient technique for isolating, culturing, and identifying vascular wall-resident CD34+ stem cells, providing an opportunity for in vitro studies on the regulatory mechanisms of VW-SCs and the screening of targeted drugs.

Introduction

The vascular wall plays a pivotal role in vascular development, homeostatic regulation, and the progression of vascular diseases. In recent years, numerous studies have unveiled the presence of various stem cell lineages in arteries. In 2004, Professor Qingbo Xu's group first reported the existence of vascular stem/progenitor cells in the periphery of the adult vascular wall, expressing CD34, Sca-1, c-kit, and Flk-11. These vascular stem cells exhibit multidirectional differentiation and proliferation potential. Under normal conditions, they remain relatively quiescent; however, when activated by specific factors, they can differentiate int....

Protocol

This study was approved, and the animals were handled in accordance with the Guidelines for the Management and Use of Laboratory Animals in China. The research strictly adhered to the ethical requirements of animal experiments, with approval from the Animal Ethics Committee (Approval Number: SWMU2020664). Eight-week-old healthy C57BL/6 mice of either gender, weighing between 18-20 g, were utilized for the present study. The animals were housed at the Laboratory Animal Center of Southwest Medical University (SWMU).

Representative Results

Isolation and purification of CD34+ VW-SCs
High purity of CD34+ VW-SCs is obtained from the adventitia of the mouse aortic and mesenteric artery by tissue attachment and magnetic microbead sorting. The percentage of CD34+ cells in the vessel wall is generally 10%-30%. Flow cytometry confirms that the purity of CD34+ cells obtained by magnetic bead sorting is more than 90% (Figure 1A). Cellular immunofluorescence staining show.......

Discussion

This study provides a quick and convenient method for obtaining functional CD34+ VW-SCs from the aorta and mesenteric arteries of mice. CD34+ VW-SCs obtained by this method have proliferative activity and multidirectional differentiation properties. Triphosphate inositol 1,4,5-trisphosphate receptors (IP3Rs), ryanodine receptors (RyRs), and store-operated calcium channels mediate Ca2+ release and entry in CD34+ VW-SCs. The establishment of this technique will lay the.......

Acknowledgements

This work was funded by grants from National Natural Science Foundation of China (No. 82070502, 31972909, 32171099), the Sichuan Science and Technology Program of Sichuan Province (23NSFSC0576, 2022YFS0607). The authors would like to thank Qingbo Xu from Zhejiang University for help with the cell culture, and the authors acknowledge the scientific and technical assistance of the flow cytometry platform in Southwest Medical University.

....

Materials

NameCompanyCatalog NumberComments
2% gelatin solutionSigmaG1393
Anti-CD31 antibodyR&DAF3628
Anti-CD34 antibodyAbcamab81289
Anti-c-kit antibodyCST77522
Anti-FITC MicroBeadsMiltenyi Biotec130-048-701 
Anti-FITC MicroBeads MACSMiltenyi Biotec130-048-701
Anti-Flk- 1 antibodyAbcamab24313
Anti-Ki67 antibodyCST34330
Anti-PDGFRα antibodyAbcamab131591
Anti-Sca- 1 antibodyInvitrogen710952
CD140a (PDGFRA) Monoclonal Antibody (APA5), FITCeBioscience  Invitrogen11-1401-82
CD31 (PECAM-1) Monoclonal Antibody (390), APCeBioscience  Invitrogen17-0311-82
CD34 Antibody, anti-mouse, FITC, REAfinity Clone REA383Miltenyi Biotec130-117-775
cell culture hoodJIANGSU SUJING GROUP CO.,LTD SW-CJ-2FD
Centrifuge  CENCE  L530
CO2 incubators            Thermofisher Scientific4111
Confocal laser scanning microscope Zeiss zeiss 980  
DMEM High Glucose MediumATCC30-2002
EBM-2 culture mediumLonzaCC-3162
FACSMelody  BD Biosciences
FACSMelody™ System BD
Fetal bovine serumMilliporeES-009-C
FM-2 culture mediumScienCell2331
Fura-2/AM InvitrogenM1292
Goat anti-Rabbit IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor Plus 488 Thermofisher Scientific   A32731
Leukemia inhibitory factorMilliporeLIF2010
Microscope OlympusIX71
MiniMACS   Starting KitMiltenyi Biotec130-090-312
Penicillin-Streptomycin-Amphotericin B SolutionBeyotimeC0224
Purified Rat Anti-Mouse CD16/CD32 (Mouse BD Fc Block)BD Pharmingen553141
Stereo Microscope OlympusSZX10 
TILLvisION 4.0 program  T.I.L.L.Photonics GmbHpolychrome V 
VWF Monoclonal Antibody (F8/86)Thermofisher Scientific MA5-14029
β-MercaptoethanolThermofisher Scientific21985023

References

  1. Hu, Y., et al. Abundant progenitor cells in the adventitia contribute to atherosclerosis of vein grafts in ApoE-deficient mice. J Clin Invest. 113 (9), 1258-1265 (2004).
  2. Jiang, L., et al.

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