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Transcriptional profiling of CD133+ cells in coronary artery disease and effects of exercise on gene expression

  • Delong Liu
  • , Alexander P. Glaser
  • , Sushmitha Patibandla
  • , Arnon Blum
  • , Peter J. Munson
  • , J. Philip McCoy
  • , Nalini Raghavachari
  • , Richard O. Cannon
  • National Institutes of Health

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

Background aims. Bone marrow (BM)-derived progenitor cells are under investigation for cardiovascular repair but may be altered by disease. Our aim was to identify differences in gene expression in CD133+ cells of patients with coronary artery disease (CAD) and healthy controls, and determine whether exercise modifies gene expression. Methods. CD133+ cells were flow-sorted from 10 CAD patients and four controls, and total RNA was isolated for microarray-based gene expression profiling. Genes that were found to be differentially regulated in patients were analyzed further to investigate whether exercise had any normalizing effect on CD133+ cells in CAD patients following 3 months of an exercise program. Results. Improvement in effort tolerance and increases in the number of CD133+ cells were observed in CAD patients after 3 months of exercise. Gene expression analysis of the CD133+ cells identified 82 differentially expressed genes (2-fold cut-off, 25% false-discovery rate and % present calls) in patients compared with controls, of which 59 were found to be up-regulated and 23 down-regulated. These genes were found to be involved in carbohydrate metabolism, cell cycle, cellular development and signaling, and molecular transport. Following completion of the exercise program, gene expression patterns resembled those of controls in seven of 10 patients. Conclusions. Alterations in gene expression of BM-derived CD133+ progenitor cells were found in CAD patients, which in part may be normalized by exercise.

Original languageEnglish
Pages (from-to)227-236
Number of pages10
JournalCytotherapy
Volume13
Issue number2
DOIs
StatePublished - Feb 2011
Externally publishedYes

Bibliographical note

Funding Information:
This research was supported by the Intramural Research Program of the NIH , National Heart, Lung and Blood Institute . We would like to acknowledge Ms Kimberly Woodhouse for her technical assistance in performing the QPCR assays.

Funding

This research was supported by the Intramural Research Program of the NIH , National Heart, Lung and Blood Institute . We would like to acknowledge Ms Kimberly Woodhouse for her technical assistance in performing the QPCR assays.

Funders
National Institutes of Health
National Heart, Lung, and Blood Institute

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Coronary artery disease
    • Exercise
    • Gene expression
    • Progenitor cells
    • Vascular repair

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