TY - JOUR
T1 - Micromanaging cardiac regeneration
T2 - Targeted delivery of microRNAs for cardiac repair and regeneration
AU - Kamps, Jan A.A.M.
AU - Krenning, Guido
PY - 2016/2/26
Y1 - 2016/2/26
N2 - The loss of cardiomyocytes during injury and disease can result in heart failure and sudden death, while the adult heart has a limited capacity for endogenous regeneration and repair. Current stem cell-based regenerative medicine approaches modestly improve cardiomyocyte survival, but offer neglectable cardiomyogenesis. This has prompted the need for methodological developments that crease de novo cardiomyocytes. Current insights in cardiac development on the processes and regulatory mechanisms in embryonic cardiomyocyte differentiation provide a basis to therapeutically induce these pathways to generate new cardiomyocytes. Here, we discuss the current knowledge on embryonic cardiomyocyte differentiation and the implementation of this knowledge in state-of-the-art protocols to the direct reprogramming of cardiac fibroblasts into de novo cardiomyocytes in vitro and in vivo with an emphasis on microRNA-mediated reprogramming. Additionally, we discuss current advances on state-of-the-art targeted drug delivery systems that can be employed to deliver these microRNAs to the damaged cardiac tissue. Together, the advances in our understanding of cardiac development, recent advances in microRNA-based therapeutics, and innovative drug delivery systems, highlight exciting opportunities for effective therapies for myocardial infarction and heart failure.
AB - The loss of cardiomyocytes during injury and disease can result in heart failure and sudden death, while the adult heart has a limited capacity for endogenous regeneration and repair. Current stem cell-based regenerative medicine approaches modestly improve cardiomyocyte survival, but offer neglectable cardiomyogenesis. This has prompted the need for methodological developments that crease de novo cardiomyocytes. Current insights in cardiac development on the processes and regulatory mechanisms in embryonic cardiomyocyte differentiation provide a basis to therapeutically induce these pathways to generate new cardiomyocytes. Here, we discuss the current knowledge on embryonic cardiomyocyte differentiation and the implementation of this knowledge in state-of-the-art protocols to the direct reprogramming of cardiac fibroblasts into de novo cardiomyocytes in vitro and in vivo with an emphasis on microRNA-mediated reprogramming. Additionally, we discuss current advances on state-of-the-art targeted drug delivery systems that can be employed to deliver these microRNAs to the damaged cardiac tissue. Together, the advances in our understanding of cardiac development, recent advances in microRNA-based therapeutics, and innovative drug delivery systems, highlight exciting opportunities for effective therapies for myocardial infarction and heart failure.
KW - PLURIPOTENT STEM-CELLS
KW - ACUTE MYOCARDIAL-INFARCTION
KW - CARDIOVASCULAR DRUG-DELIVERY
KW - CARDIOMYOCYTE-LIKE CELLS
KW - HEART FIELD DEVELOPMENT
KW - MUSCLE GENE-EXPRESSION
KW - IN-VIVO
KW - HUMAN FIBROBLASTS
KW - PROGENITOR CELLS
KW - MAMMALIAN HEART
U2 - 10.4330/wjc.v8.i2.163
DO - 10.4330/wjc.v8.i2.163
M3 - Article
C2 - 26981212
VL - 8
SP - 163
EP - 179
JO - World Journal of Cardiology
JF - World Journal of Cardiology
IS - 2
ER -