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Apoptosis in right-ventricle biopsy is not predictive of graft survival
L Chalabreysse1, C Leroux, J-F Obadia
1Department of Pathology, Hôpital Louis Pradel, BP Lyon Montchat 69 394, Cedex 03 Lyon, France. lara.chalabreysse@chu-lyon.fr
Insights
Brain death can cause cell death in donor hearts, but this pre-existing apoptosis does not predict heart transplant dysfunction. Researchers examined donor and control hearts for signs of cell death to understand transplant outcomes.
Area of Science:
- Cardiology
- Transplantation Immunology
- Cell Biology
Background:
- Myocardial dysfunction is a frequent complication in heart grafts from brain-dead donors.
- The underlying mechanisms contributing to this dysfunction are not fully understood.
- Apoptosis (programmed cell death) has been proposed as a potential factor.
Purpose of the Study:
- To investigate the presence of apoptotic myocardial cells in brain-dead donor hearts.
- To compare apoptosis levels in donor hearts versus control hearts.
- To determine if pre-existing apoptosis in donor hearts predicts post-transplant myocardial dysfunction.
Main Methods:
- Apoptosis was assessed using an in situ DNA fragmentation assay.
- Western Blotting was employed to detect caspase-3, a key enzyme in the apoptotic pathway.
- Donor hearts were compared to control hearts.
Main Results:
- Brain death was found to induce myocardial apoptosis in donor hearts.
- However, the levels of apoptosis detected in donor hearts did not correlate with the development of myocardial dysfunction after transplantation.
- Caspase-3 activation was observed, confirming apoptotic activity.
Conclusions:
- Myocardial apoptosis induced by brain death is present in donor hearts.
- Pre-existing apoptosis in donor hearts is not a reliable predictor of myocardial dysfunction following heart transplantation.
- Further research is needed to identify the precise mechanisms of graft dysfunction.
Abstract:
Myocardial dysfunction is common in grafted hearts from brain-dead donors, but the mechanisms involved remain unclear, although apoptosis has been suggested to play an important role. In this study, we investigated the presence of apoptotic myocardial cells in donor hearts as compared to control hearts to determine whether pre-existing apoptosis can predict donor heart dysfunction. Apoptosis was studied by in situ DNA fragmentation assay and by Western Blotting for caspase-3, the pivotal executive caspase of the apoptotic pathway. We show that brain-death induced myocardial apoptosis was not predictive of myocardial dysfunction in transplanted hearts.
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