Xenografted Adult Human Mesenchymal Stem Cells Provide a Platform for Sustained Biological Pacemaker Function in Canine Heart
Author(s) -
Alexei N. Plotnikov,
Iry. Shlapakova,
Matthias Szabolcs,
Peter Danilo,
Beverly H. Lorell,
Irina A. Potapova,
Zhongju Lu,
Amy B. Rosen,
Richard T. Mathias,
Peter R. Brink,
Richard B. Robinson,
Ira S. Cohen,
Michael R. Rosen
Publication year - 2007
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.107.703231
Subject(s) - mesenchymal stem cell , medicine , embryonic stem cell , stem cell , andrology , xenotransplantation , transfection , immunosuppression , transplantation , microbiology and biotechnology , immunology , endocrinology , cell culture , biology , pathology , biochemistry , genetics , gene
Biological pacemaking has been performed with viral vectors, human embryonic stem cells, and adult human mesenchymal stem cells (hMSCs) as delivery systems. Only with human embryonic stem cells are data available regarding stability for >2 to 3 weeks, and here, immunosuppression has been used to facilitate survival of xenografts. The purpose of the present study was to determine whether hMSCs provide stable impulse initiation over 6 weeks without the use of immunosuppression, the "dose" of hMSCs that ensures function over this period, and the catecholamine responsiveness of hMSC-packaged pacemakers.
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