The Journal of Thoracic and Cardiovascular Surgery
Volume 139, Issue 6 , Pages 1637-1643, June 2010

Orthotopic vascularized right lung transplantation in the mouse

  • Wenjun Li, MD

      Affiliations

    • Department of Surgery, Washington University, St Louis, Mo
  • ,
  • Seiichiro Sugimoto, MD, PhD

      Affiliations

    • Department of Surgery, Washington University, St Louis, Mo
  • ,
  • Jiaming Lai, MD

      Affiliations

    • Department of Surgery, Washington University, St Louis, Mo
  • ,
  • G. Alexander Patterson, MD

      Affiliations

    • Department of Surgery, Washington University, St Louis, Mo
  • ,
  • Andrew E. Gelman, PhD

      Affiliations

    • Department of Surgery, Washington University, St Louis, Mo
    • Department of Pathology and Immunology, Washington University, St Louis, Mo
  • ,
  • Alexander S. Krupnick, MD

      Affiliations

    • Department of Surgery, Washington University, St Louis, Mo
  • ,
  • Daniel Kreisel, MD, PhD

      Affiliations

    • Department of Surgery, Washington University, St Louis, Mo
    • Department of Pathology and Immunology, Washington University, St Louis, Mo
    • Corresponding Author InformationAddress for reprints: Daniel Kreisel, MD, PhD, Departments of Surgery and Pathology and Immunology, Campus Box 8234, 660 South Euclid Ave, Washington University in St Louis, St Louis, MO 63110-1013.

Received 28 July 2009; received in revised form 15 October 2009; accepted 12 November 2009. published online 10 March 2010.

Objectives

Orthotopic left lung transplantation in the mouse, as recently developed by our laboratory, represents a physiologic model for studies in transplantation biology. However, because of the limited overall respiratory contribution of the murine left lung, left lung transplant recipients remain healthy despite immune-mediated graft necrosis. We sought to develop a lung transplantation model in which animal survival depends on graft function.

Methods

Orthotopic vascularized right lung transplantations using cuff techniques were performed in syngeneic and allogeneic strain combinations. Grafts were assessed histologically or functionally by measuring arterial blood gases from 7 to 28 days after transplantation. In a parallel set of experiments, syngeneic and immunosuppressed allogeneic hosts underwent a left pneumonectomy 2 weeks after right lung transplantation, with assessment of graft function 1 week later.

Results

We performed 40 right lung transplantations, with a survival rate of 87.5%. Syngeneic grafts remain free of inflammation as far as 28 days after transplantation. On day 7, arterial oxygen levels in syngeneic recipients (481 ± 90 mm Hg) are equivalent to those in naive mice (503 ± 59 mm Hg) after left hilar occlusion. Alternatively, allogeneic grafts develop histologic evidence of acute rejection, and arterial oxygen levels are significantly decreased after left hilar clamping (53.3 ± 10.3 mm Hg). Both syngeneic and immunosuppressed allogeneic right lung recipients tolerate a left pneumonectomy.

Conclusions

Right lung transplantation followed by left pneumonectomy represents the first survival model of vascularized lung transplantation in the mouse and will therefore allow for the design of novel studies in experimental lung transplantation.

CTSNet classification: 12

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 Dr Kreisel is supported by a grant jointly sponsored by the National Heart, Lung, and Blood Institute and the Thoracic Surgery Foundation for Research and Education (1K08HL083983) and by a grant from the National Heart, Lung, and Blood Institute (1R01HL094601).

 Disclosures: None.

PII: S0022-5223(09)01474-3

doi:10.1016/j.jtcvs.2009.11.019

The Journal of Thoracic and Cardiovascular Surgery
Volume 139, Issue 6 , Pages 1637-1643, June 2010