TY - JOUR
T1 - Cardiomyocytes undergo cells division following myocardial infarction is a spatially and temporally restricted event in rats
AU - Yuasa, Shinsuke
AU - Fukuda, Keiichi
AU - Tomita, Yuichi
AU - Fujita, Jun
AU - Ieda, Masaki
AU - Tahara, Satoko
AU - Itabashi, Yuji
AU - Yagi, Takashi
AU - Kawaguchi, Haruko
AU - Hisaka, Yasuyo
AU - Ogawa, Satoshi
N1 - Funding Information:
This study was supported in part by research grants from the Ministry of Education, Science and Culture, Japan, and Health Science Research Grants for Advanced Medical Technology from the Ministry of Welfare, Japan. This work was presented at the second Annual Meeting of the IACS Japan Section.
PY - 2004/4
Y1 - 2004/4
N2 - Dividing cardiomyocytes are observed in autopsied human hearts following recent myocardial infarction, however there is a lack of information in the literature on the division of these cells. In this study we used a rat model to investigate how and when adult mammalian cardiomyocytes proliferate by cell division after myocardial infarction. Myocardial infarction was induced in Wistar rats by ligation of the left coronary artery. The rats were sacrificed periodically up to 28 days following induced myocardial infarction, and the hearts subjected to microscopic investigation. Cardiomyocytes entering the cell cycle were assayed by observation of nuclear morphology and measuring expression of Ki-67, a proliferating cell marker. Ki-67 positive cardiomyocytes and dividing nuclei were observed initially after 1 day. After 2 days dividing cells gradually increased in number at the ischemic border zone, reaching a peak increase of 1.12% after 3 days, then gradually decreasing in number. Dividing nuclei increased at the ischemic border zone after 3 days, peaked by 0.14% at day 5, and then decreased. In contrast, Ki-67 positive cells and dividing nuclei were limited in number in the non-ischemic area throughout all experiments. In conclusion, mitogenic cardiomyocytes are present in the adult rat heart following myocardial infarction, but were spatially and temporally restricted.
AB - Dividing cardiomyocytes are observed in autopsied human hearts following recent myocardial infarction, however there is a lack of information in the literature on the division of these cells. In this study we used a rat model to investigate how and when adult mammalian cardiomyocytes proliferate by cell division after myocardial infarction. Myocardial infarction was induced in Wistar rats by ligation of the left coronary artery. The rats were sacrificed periodically up to 28 days following induced myocardial infarction, and the hearts subjected to microscopic investigation. Cardiomyocytes entering the cell cycle were assayed by observation of nuclear morphology and measuring expression of Ki-67, a proliferating cell marker. Ki-67 positive cardiomyocytes and dividing nuclei were observed initially after 1 day. After 2 days dividing cells gradually increased in number at the ischemic border zone, reaching a peak increase of 1.12% after 3 days, then gradually decreasing in number. Dividing nuclei increased at the ischemic border zone after 3 days, peaked by 0.14% at day 5, and then decreased. In contrast, Ki-67 positive cells and dividing nuclei were limited in number in the non-ischemic area throughout all experiments. In conclusion, mitogenic cardiomyocytes are present in the adult rat heart following myocardial infarction, but were spatially and temporally restricted.
KW - Cardiomyocyte
KW - Cell division
KW - Ki-67
KW - Myocardial infarction
KW - Regeneration
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U2 - 10.1023/B:MCBI.0000021370.24453.0c
DO - 10.1023/B:MCBI.0000021370.24453.0c
M3 - Article
C2 - 15124922
AN - SCOPUS:11144356400
SN - 0300-8177
VL - 259
SP - 177
EP - 181
JO - Molecular and Cellular Biochemistry
JF - Molecular and Cellular Biochemistry
IS - 1-2
ER -