Chimerism in Human Hearts
Recent evidence suggests extracardiac progenitors can repopulate
injured human hearts to replace damaged cells. One method of investigating
this observation is to perform in-situ hybridization techniques in
sex-mismatched heart transplants. We studied human female donor hearts
that were transplanted into male recipients and assessed the degree of
recipient cells with Y chromosome in-situ hybridization. Using this
technique, our lab has recently published data showing evidence that
extracardiac progenitor cells from the recipient replace damaged cardiomyocytes
in transplanted hearts. (Circulation Research)
Applying this technique, we also observed that major cell types in the
heart are repopulated to a variable degree by recipient cells. However,
the exact source of these progenitors is still under investigation.
We are currently underway to set up a mouse transplant model that would allow
further investigation into the source of these cells. If we are able to define,
select, and control these progenitor cells, the myocardial repair process can be
enhanced, which can potentially lead to application in the clinical setting.
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