The Journal of Heart and Lung Transplantation
Volume 27, Issue 7 , Pages 701-709, July 2008

Increased Expression of Stem Cell Factor and Its Receptor After Left Ventricular Assist Device Support: A Potential Novel Target for Therapeutic Interventions in Heart Failure

  • Jama Jahanyar, MD, PhD

      Affiliations

    • Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas
    • Corresponding Author InformationReprint requests: Jama Jahanyar, MD, PhD, Michael E. DeBakey Department of Surgery, Division of Transplant and Assist Devices, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030. Telephone: 713-790-3155. Fax: 713-797-0613.
  • ,
  • Keith A. Youker, PhD

      Affiliations

    • Methodist DeBakey Heart Center, The Methodist Hospital, Houston, Texas
  • ,
  • Guillermo Torre-Amione, MD, PhD

      Affiliations

    • Methodist DeBakey Heart Center, The Methodist Hospital, Houston, Texas
  • ,
  • Michael M. Koerner, MD, PhD

      Affiliations

    • Department of Medicine, Section of Cardiology, Baylor College of Medicine and Texas Heart Institute, Houston, Texas.
  • ,
  • Brian Bruckner, MD

      Affiliations

    • Methodist DeBakey Heart Center, The Methodist Hospital, Houston, Texas
  • ,
  • George P. Noon, MD

      Affiliations

    • Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas
    • Methodist DeBakey Heart Center, The Methodist Hospital, Houston, Texas
  • ,
  • Matthias Loebe, MD, PhD

      Affiliations

    • Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas
    • Methodist DeBakey Heart Center, The Methodist Hospital, Houston, Texas

Received 6 November 2007; received in revised form 8 February 2008; accepted 27 March 2008. published online 03 June 2008.

Background

Left ventricular assist devices (LVADs) cause an influx of mast cells into the failing heart, but the underlying mechanism is unknown. This study investigates the potential role of stem cell factor (SCF) and its receptor (c-Kit) in promoting the recruitment of mast cells during heart failure and after LVAD support.

Methods

Myocardial samples were collected from 10 end-stage heart failure patients undergoing LVAD implantation (pre-LVAD) and paired with samples taken at the time of orthotopic heart transplantation (post-LVAD). Biopsies of normal hearts served as controls. We assessed gene expression of SCF and c-Kit. In addition, we stained for SCF, c-Kit, tryptase and chymase, and utilized in situ hybridization to determine the origin of SCF.

Results

SCF mRNA and overall mast cell numbers were significantly increased (p < 0.01/p < 0.001) after LVAD support as compared with paired heart failure tissues. c-Kit mRNA was significantly increased post-LVAD compared with normal tissues (p < 0.05). The c-Kit protein was expressed only in cardiac mast cells. SCF mRNA was found in endothelial cells, myocytes and interstitial cells, as confirmed by antibody staining.

Conclusions

LVADs cause an increase of SCF and c-Kit gene expression, which coincides with a surge of mast cells after ventricular unloading. This suggests that SCF functions as an important mediator for the recruitment of mast cells to the mechanically unloaded human heart.

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 Supported by the George P. Noon Research Fund and the Michael E. DeBakey Foundation.

PII: S1053-2498(08)00283-0

doi:10.1016/j.healun.2008.03.021

The Journal of Heart and Lung Transplantation
Volume 27, Issue 7 , Pages 701-709, July 2008