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Published Online: 3 December 2018

Controlled Release of Small Molecules for Cardiac Differentiation of Pluripotent Stem Cells

Publication: Tissue Engineering Part A
Volume 24, Issue Number 23-24

Abstract

Induced pluripotent stem cells (iPSCs) have been shown to differentiate to functional cardiomyocytes (CM) with high efficiency through temporally controlled inhibition of the GSK3/Wnt signaling pathways. In this study, we investigated the ability of temporally controlled release of GSK3/Wnt small-molecule inhibitors to drive cardiac differentiation of iPSC without manual intervention. Porous silica particles were loaded with GSK3 inhibitor CHIR99021 or Wnt inhibitor IWP2, and the particles containing IWP2 were coated with 5 wt% poly(lactic-co-glycolic acid) 50:50 to delay release by ∼72 h. iPSCs reprogrammed through mRNA transfection were cultured with these particles up to 30 days. High-performance liquid chromatography suggests a burst release of CHIR99021 within the first 24 h and a delayed release of IWP2 after 72 h. Annexin V/propidium iodide staining did not show a significant effect on apoptosis or necrosis rates. Cultured cells upregulated both early (Nkx 2.5, Isl-1) and late (cTnT, MHC, Cx43) cardiac markers, assayed with a quantitative real-time polymerase chain reaction, and began spontaneous contraction at 3.0 ± 0.6 Hz at 15–21 days after the start of differentiation. CM had clear sarcomeric striations when stained for β-myosin heavy chain, and showed expression and punctate membrane localization of gap junction protein Connexin43. Calcium and voltage-sensitive imaging showed both action potential and calcium transients typical of immature CM. This study showed that the cardiac differentiation of pluripotent stem cells can be directed by porous silica vectors with temporally controlled release of small-molecule inhibitors. These results suggest methods for automating and eliminating variability in manual maintenance of inhibitor concentrations in the differentiation of pluripotent stem cells to CM.

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Information & Authors

Information

Published In

cover image Tissue Engineering Part A
Tissue Engineering Part A
Volume 24Issue Number 23-24December 2018
Pages: 1798 - 1807
PubMed: 30129882

History

Published online: 3 December 2018
Published in print: December 2018
Published ahead of print: 29 October 2018
Published ahead of production: 21 August 2018
Accepted: 4 June 2018
Received: 12 February 2018

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Christopher J. Tsao
Department of Bioengineering, Rice University, Houston, Texas.
Francesca Taraballi
Department of Regenerative Medicine, Houston Methodist Research Institute, Houston, Texas.
Laura Pandolfi
Department of Regenerative Medicine, Houston Methodist Research Institute, Houston, Texas.
Aaron J. Velasquez-Mao
Department of Bioengineering, Rice University, Houston, Texas.
Rodrigo Ruano
Department of Obstetrics and Gynecology, Fetal Diagnostic and Intervention Center, Rochester, Minnesota.
Ennio Tasciotti
Department of Regenerative Medicine, Houston Methodist Research Institute, Houston, Texas.
Jeffrey G. Jacot [email protected]
Department of Bioengineering, Rice University, Houston, Texas.
Congenital Heart Surgery Service, Texas Children's Hospital, Houston, Texas.
Department of Bioengineering, University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado.

Notes

Address correspondence to: Jeffrey G. Jacot, PhD, Department of Bioengineering, University of Colorado Denver, Anschutz Medical Campus, 12705 E. Montview Avenue, Suite 100, Aurora, CO 80045 [email protected]

Disclosure Statement

No competing financial interests exist.

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