Placenta as a source for progenitor cells for cardiac cell-based therapies

Abstract

Objective: Cell-based therapies utilizing mesenchymal and cardiac progenitor cells have demonstrated promising results in the treatment of congenital heart disease. We hypothesize that autologous human placental-derived progenitor cells share similar characteristics to cardiac progenitor cells (CPC) derived from autologous bone marrow or cardiac sources.Methods: Fetal portion of the placenta was harvested at the time of delivery from newborns (N = 5), and cells were isolated and expanded from the amnion and chorion layers. Flow cytometry and multi-lineage differentiation potential assays were used to characterize placental-derived progenitor cells. Placenta derived sphere cells were generated and phenotypic and functional characteristics were analyzed.Results: CD90, CD105, and Vimentin were expressed in 65% expressed cardiac lineage marker (SIRPA), but <15% expressed Discoidin domain receptor 2 (DDR2). Compared to placental-derived progenitor cells, placenta derived sphere cells expressed higher levels of cardiac transcription factors, cardiac ion channel genes and cardiac structural genes.Conclusions: Placental progenitor cells demonstrate similar characteristics to CPC currently utilized in several clinical trials that can serve as a readily available autologous source for cardiac cell therapy.

Keywords

• Congenital heart surgery
• Placenta
• Stem cells