TY - JOUR
T1 - Progress and challenges of amniotic fluid derived stem cells in therapy of ischemic heart disease
AU - Fang, Yi Hsien
AU - Wang, Saprina P.H.
AU - Chang, Hsien Yuan
AU - Yang, Pei Jung
AU - Liu, Ping Yen
AU - Liu, Yen Wen
N1 - Funding Information:
Acknowledgments: This review article was funded by grants from Ministry of Science and Technology, Taiwan (MOST 109-2628-B-006-028). We thank the Research Center of Clinical Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University for professional domain knowledge consultation and writing guidance.
Funding Information:
This review article was funded by grants from the Ministry of Science and Technology, Taiwan [MOST 108-2628-B-006-020]. This review article was funded by grants from Ministry of Science and Technology, Taiwan (MOST 109-2628-B-006-028). We thank the Research Center of Clinical Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University for professional domain knowledge consultation and writing guidance.
Funding Information:
Funding: This review article was funded by grants from the Ministry of Science and Technology, Taiwan [MOST 108-2628-B-006-020].
Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/1/1
Y1 - 2021/1/1
N2 - Cardiovascular disease is the leading cause of deaths worldwide, claiming an estimated total of 17.9 million lives each year, of which one-third of the people are under the age of 70 years. Since adult cardiomyocytes fail to regenerate, the heart loses the ability to repair itself after an injury, making patients with heart disease suffer from poor prognosis. Pluripotent stem cells have the ability to differentiate into cardiomyocytes in vitro through a well-established process, which is a new advancement in cardiac regeneration therapy. However, pluripotent stem cell-derived cardiomyocytes have certain drawbacks, such as the risk of arrhythmia and immune incompatibility. Thus, amniotic fluid stem cells (AFSCs), a relatively novel source of stem cells, have been exploited for their ability of pluripotent differentiation. In addition, since AFSCs are weakly positive for the major histocompatibility class II molecules, they may have high immune tolerance. In summary, the possibility of development of cardiomyocytes from AFSCs, as well as their transplantation in host cells to produce mechanical contraction, has been discussed. Thus, this review article highlights the progress of AFSC therapy and its application in the treatment of heart diseases in recent years.
AB - Cardiovascular disease is the leading cause of deaths worldwide, claiming an estimated total of 17.9 million lives each year, of which one-third of the people are under the age of 70 years. Since adult cardiomyocytes fail to regenerate, the heart loses the ability to repair itself after an injury, making patients with heart disease suffer from poor prognosis. Pluripotent stem cells have the ability to differentiate into cardiomyocytes in vitro through a well-established process, which is a new advancement in cardiac regeneration therapy. However, pluripotent stem cell-derived cardiomyocytes have certain drawbacks, such as the risk of arrhythmia and immune incompatibility. Thus, amniotic fluid stem cells (AFSCs), a relatively novel source of stem cells, have been exploited for their ability of pluripotent differentiation. In addition, since AFSCs are weakly positive for the major histocompatibility class II molecules, they may have high immune tolerance. In summary, the possibility of development of cardiomyocytes from AFSCs, as well as their transplantation in host cells to produce mechanical contraction, has been discussed. Thus, this review article highlights the progress of AFSC therapy and its application in the treatment of heart diseases in recent years.
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U2 - 10.3390/ijms22010102
DO - 10.3390/ijms22010102
M3 - Article
C2 - 33374215
AN - SCOPUS:85098700113
SN - 1661-6596
VL - 22
SP - 1
EP - 12
JO - International journal of molecular sciences
JF - International journal of molecular sciences
IS - 1
M1 - 102
ER -