TY - JOUR
T1 - Creating frog heart as an organ
T2 - In vitro-induced heart functions as a circulatory organ in vivo
AU - Kinoshita, Masayoshi
AU - Ariizumi, Takashi
AU - Yuasa, Shinsuke
AU - Miyoshi, Shunichirou
AU - Komazaki, Shinji
AU - Fukuda, Keiichi
AU - Asashima, Makoto
PY - 2010
Y1 - 2010
N2 - Cardiomyocytes have been induced from various pluripotent cells, such as embryonic stem cells and myeloid stem cells; however, the generation of cardiac tissues beyond two-dimensional cell-sheets has not been reported. Creating higher order, three-dimensional structures that are unique to heart is the long-awaited next step in realizing cardiac regenerative medicine. We have previously shown that cardiomyocytes can be induced in vitro from undifferentiated cells (animal caps) excised from Xenopus embryos. Cardiomyocytes were induced by first dissociating the animal caps and then reaggregating them following treatment with activin. Here, we describe an interesting method for creating a complete ectopic heart in vivo, involving the introduction of in vitro-created tissue during early embryogenesis. Thus, animal cap reaggregates were transplanted into the abdomen of late-neurula-stage embryos, resulting in two-chambered hearts being formed. The dual-heart larvae matured into adult animals with transplanted hearts intact. Involvement of transplanted hearts in systemic circulation was demonstrated. Moreover, the ectopic hearts possessed higher order structures such as atrium and ventricle, and were morphologically, histologically, and electrophysiologically identical to original hearts. This system should facilitate the study of heart organogenesis and may promote a shift from tissue to organ engineering for clinical applications.
AB - Cardiomyocytes have been induced from various pluripotent cells, such as embryonic stem cells and myeloid stem cells; however, the generation of cardiac tissues beyond two-dimensional cell-sheets has not been reported. Creating higher order, three-dimensional structures that are unique to heart is the long-awaited next step in realizing cardiac regenerative medicine. We have previously shown that cardiomyocytes can be induced in vitro from undifferentiated cells (animal caps) excised from Xenopus embryos. Cardiomyocytes were induced by first dissociating the animal caps and then reaggregating them following treatment with activin. Here, we describe an interesting method for creating a complete ectopic heart in vivo, involving the introduction of in vitro-created tissue during early embryogenesis. Thus, animal cap reaggregates were transplanted into the abdomen of late-neurula-stage embryos, resulting in two-chambered hearts being formed. The dual-heart larvae matured into adult animals with transplanted hearts intact. Involvement of transplanted hearts in systemic circulation was demonstrated. Moreover, the ectopic hearts possessed higher order structures such as atrium and ventricle, and were morphologically, histologically, and electrophysiologically identical to original hearts. This system should facilitate the study of heart organogenesis and may promote a shift from tissue to organ engineering for clinical applications.
KW - Activin
KW - Animal cap
KW - Cardiogenesis
KW - Organ engineering
KW - Xenopus laevis
UR - http://www.scopus.com/inward/record.url?scp=77956026761&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=77956026761&partnerID=8YFLogxK
U2 - 10.1387/ijdb.093036mk
DO - 10.1387/ijdb.093036mk
M3 - Article
C2 - 20336605
AN - SCOPUS:77956026761
SN - 0214-6282
VL - 54
SP - 851
EP - 856
JO - International Journal of Developmental Biology
JF - International Journal of Developmental Biology
IS - 5
ER -