Exosomes as critical agents of cardiac regeneration triggered by cell therapy

Ahmed Gamal Eldin Ibrahim, Ke Cheng, Eduardo Marbán

Research output: Contribution to journalArticle

Abstract

The CADUCEUS trial of cardiosphere-derived cells (CDCs) has shown that it may be possible to regenerate injured heart muscle previously thought to be permanently scarred. The mechanisms of benefit are known to be indirect, but the mediators have yet to be identified. Here we pinpoint exosomes secreted by human CDCs as critical agents of regeneration and cardioprotection. CDC exosomes inhibit apoptosis and promote proliferation of cardiomyocytes, while enhancing angiogenesis. Injection of exosomes into injured mouse hearts recapitulates the regenerative and functional effects produced by CDC transplantation, whereas inhibition of exosome production by CDCs blocks those benefits. CDC exosomes contain a distinctive complement of microRNAs, with particular enrichment of miR-146a. Selective administration of a miR-146a mimic reproduces some (but not all) of the benefits of CDC exosomes. The findings identify exosomes as key mediators of CDC-induced regeneration, while highlighting the potential utility of exosomes as cell-free therapeutic candidates.

Original languageEnglish (US)
Pages (from-to)606-619
Number of pages14
JournalStem Cell Reports
Volume2
Issue number5
DOIs
StatePublished - May 6 2014
Externally publishedYes

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Exosomes
Cell- and Tissue-Based Therapy
Regeneration
MicroRNAs
Muscle
Apoptosis
Cell Transplantation
Cardiac Myocytes
Myocardium
Injections

ASJC Scopus subject areas

  • Biochemistry
  • Cell Biology
  • Developmental Biology
  • Genetics

Cite this

Exosomes as critical agents of cardiac regeneration triggered by cell therapy. / Ibrahim, Ahmed Gamal Eldin; Cheng, Ke; Marbán, Eduardo.

In: Stem Cell Reports, Vol. 2, No. 5, 06.05.2014, p. 606-619.

Research output: Contribution to journalArticle

Ibrahim, Ahmed Gamal Eldin ; Cheng, Ke ; Marbán, Eduardo. / Exosomes as critical agents of cardiac regeneration triggered by cell therapy. In: Stem Cell Reports. 2014 ; Vol. 2, No. 5. pp. 606-619.
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