|
An estimated 275,000 patients undergo heart
valve replacement each year. However, existing
solutions for valve replacement are complicated
by the morbidity associated with lifelong
anticoagulation of mechanical valves and the
limited durability of bioprostheses. Recent
advances in tissue engineering and our
understanding of stem cell biology may provide a
lifelong solution to these problems.
Mesenchymal stem cells were isolated from ovine
bone marrow and characterized by their
morphology and antigen expression through
immunocytochemistry, flow cytometry, and
capacity to differentiate into multiple cell
lineages. A biodegradable scaffold was developed
and characterized by its tensile strength and
stiffness as a function of time in
cell-conditioned medium. Autologous semilunar
heart valves were then created in vitro using
mesenchymal stem cells and the biodegradable
scaffold and were implanted into the pulmonary
position of sheep on cardiopulmonary bypass.
The valves were evaluated by echocardiography at
implantation and after 4 months in vivo. Valves
were explanted at 4 and 8 months and examined by
histology and immunohistochemistry. Valves
displayed a maximum instantaneous gradient of
17.2 ± 1.33 mm Hg, a mean gradient of 9.7 ± 1.3
mm Hg, an effective orifice area of 1.35 ± 0.17
cm2, and trivial or mild regurgitation at
implantation. Gradients changed little over 4
months of follow-up. Histology showed
disposition of extracellular matrix and
distribution of cell phenotypes in the
engineered valves reminiscent of that in native
pulmonary valves.
Stem-cell tissue-engineered heart valves can be
created from mesenchymal stem cells in
combination with a biodegradable scaffold and
function satisfactorily in vivo for periods of >
4 months. Furthermore, such valves undergo
extensive remodeling in vivo to resemble native
heart valves.
Circulation. 2005;111:2783-2791
|