Journal of Molecular and Cellular Cardiology
Volume 44, Issue 3 , Pages 486-495, March 2008

Comparison of intracoronary and transendocardial delivery of allogeneic mesenchymal cells in a canine model of acute myocardial infarction

  • Emerson C. Perin

      Affiliations

    • The Texas Heart Institute at St. Luke's Episcopal Hospital, Houston, TX 77030, USA
    • Corresponding Author InformationCorresponding author. Tel.: +1 713 791 9400; fax: +1 713 795 5651.
  • ,
  • Guilherme V. Silva

      Affiliations

    • The Texas Heart Institute at St. Luke's Episcopal Hospital, Houston, TX 77030, USA
  • ,
  • Joao A.R. Assad

      Affiliations

    • The Texas Heart Institute at St. Luke's Episcopal Hospital, Houston, TX 77030, USA
  • ,
  • Deborah Vela

      Affiliations

    • The Texas Heart Institute at St. Luke's Episcopal Hospital, Houston, TX 77030, USA
    • The University of Texas Health Science Center at Houston, Houston, TX 77030, USA
  • ,
  • L. Maximilian Buja

      Affiliations

    • The Texas Heart Institute at St. Luke's Episcopal Hospital, Houston, TX 77030, USA
    • The University of Texas Health Science Center at Houston, Houston, TX 77030, USA
  • ,
  • Andre L.S. Sousa

      Affiliations

    • The Texas Heart Institute at St. Luke's Episcopal Hospital, Houston, TX 77030, USA
  • ,
  • Silvio Litovsky

      Affiliations

    • The Texas Heart Institute at St. Luke's Episcopal Hospital, Houston, TX 77030, USA
  • ,
  • Jing Lin

      Affiliations

    • The Texas Heart Institute at St. Luke's Episcopal Hospital, Houston, TX 77030, USA
  • ,
  • William K. Vaughn

      Affiliations

    • The Texas Heart Institute at St. Luke's Episcopal Hospital, Houston, TX 77030, USA
  • ,
  • Stephanie Coulter

      Affiliations

    • The Texas Heart Institute at St. Luke's Episcopal Hospital, Houston, TX 77030, USA
  • ,
  • Marlos R. Fernandes

      Affiliations

    • The Texas Heart Institute at St. Luke's Episcopal Hospital, Houston, TX 77030, USA
    • The University of Texas Health Science Center at Houston, Houston, TX 77030, USA
  • ,
  • James T. Willerson

      Affiliations

    • The Texas Heart Institute at St. Luke's Episcopal Hospital, Houston, TX 77030, USA
    • The University of Texas Health Science Center at Houston, Houston, TX 77030, USA

Received 2 July 2007; received in revised form 30 August 2007; accepted 27 September 2007.

Abstract 

This study assessed safety of transendocardial (TE) electromechanical-guided delivery of bone marrow mesenchymal stem cells (MSCs) after acute myocardial infarction (AMI) and compared intracoronary (IC) delivery with TE delivery. In a canine acute myocardial ischemia model, 100×106 MSCs were delivered 7 days after AMI via IC and TE routes. Functional assessment was performed by 2D echocardiogram, and detailed histopathologic analyses were performed to assess the impact of cell therapy in vascular density and fibrosis. Patterns of cell distribution in both delivery methods were also compared. There was a statistically significant reduction in the amount of myocardial ischemia in the TE group (P=0.007). Left ventricular ejection fraction (LVEF) increased 13% (mean) in the TE group (21-day follow-up) and was significantly better than that of the controls (P=0.01), but did not improve in the IC-delivery group. Dissimilar patterns of cell distribution were noted between the IC and TE groups. This study suggests that MSC treatment is probably safe and effective after AMI. In the comparison of TE and IC delivery, the TE group showed higher cell retention (clusters even in the injury center of the infarct) with an increased vascularity and greater functional improvement than did the IC group (no clusters; cells at the border of the infarct). The higher local cell density in the TE group may be important for therapeutic effectiveness.

Keywords: Acute myocardial infarction, Stem cell therapy, Transendocardial delivery, Intracoronary delivery, Mesenchymal stem cell, Stem cell injection

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PII: S0022-2828(07)01241-2

doi:10.1016/j.yjmcc.2007.09.012

Journal of Molecular and Cellular Cardiology
Volume 44, Issue 3 , Pages 486-495, March 2008