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Project III

YING MEI, PhD Assistant Professor of Bioengineering  Clemson University MUSC CampusPolymer Microarrays for Stem Cell Cardiac Differentiation

Target Investigator

Assistant Professor of Bioengineering

Clemson University MUSC Campus

Phone: 843-876-2548

Polymer Microarrays for stem cell Cardiac Regeneration

Cardiovascular disease, the leading cause of death and disability worldwide, claims more lives than all kinds of cancers combined. Ischaemic heart disease (IHD) and myocardial infarction (MI) are major contributors to cardiovascular morbidity and mortality; they usually are associated with irreversible death of cardiomyocyte and lead to permanent loss of heart function. Human embryonic stem cell (hESC) and human induced pluripotent stem cell (hIPSC) technologies hold remarkable promise for myocardial regeneration because of their unquestionable capacity to produce de novo cardiomyocytes.

Two key limitations of existing hESC and hIPSC technology are:

  • The lack of chemically defined, completely synthetic substrates to derive clinical grade cardiac cells.
  • The suboptimal efficiency associated with stem-cell differentiation into cardiac cells.

Synthetic short peptides derived from extracellular matrix (ECM) proteins and growth factors have been extensively used to enhance cell adhesion and proliferation on synthetic materials. However, their low affinity for cell-surface receptors limits their ability to direct stem-cell differentiation. Using my expertise in peptide synthesis, polymer science, combinatorial approach, and hESC and hIPSC technology, I propose to develop completely synthetic, biologically functional substrates to direct hESCs and hIPSCs to differentiate into clinical-grade cardiomyocytes in a xeno-free, chemically defined condition.

The central hypothesis of this project is that the substrates with a variety of high density peptides derived from multiple cardiogenic ECM proteins and growth factors that are essential to cardiogenesis can effectively induce cardiac differentiation of hESCs and hIPSCs through high affinity, synergic engagements between peptides and cell-surface receptors.