Grants and Contracts Details
Description
Recent evidence indicates that mobilized bone marrow (BM)-derived stem/progenitor cells
(SPCs) contribute to dynamic cardiomyocyte chimerism under physiological conditions and
after acute myocardial infarction (AMI), mostly through paracrine effects. While it is clear that
the magnitude of BMSPCs mobilization following AMI correlates with cardiac recovery, the
molecular events driving BMSPC mobilization and homing are poorly understood. There is
a critical need to define the pathways responsible for the mobilization and homing of
BMSPCs following AMI and ultimately their regenerative capacity. In the absence of such
knowledge, the promise of ultimately developing innovative mechanism-based strategies to
treat and/or prevent AMI-induced cardiac injury will remain unlikely.
Our long-term research goal is to contribute toward the development of new clinically useful
myocardial regenerative therapies for injury caused by AMI.
Status | Finished |
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Effective start/end date | 9/1/14 → 12/31/15 |
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