Cardiac telocytes were decreased during myocardial infarction and their therapeutic effects for ischaemic heart in rat.
Cardiac telocytes were decreased during myocardial infarction and their therapeutic effects for ischaemic heart in rat.
复制标题
心肌梗死时心肌细胞减少及其对大鼠缺血性心脏的治疗作用
DOI:
10.1111/j.1582-4934.2012.01655.x
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发表时间:
2013-01
影响因子:
5.3
通讯作者:
Cai D
中科院分区:
文献类型:
--
作者:
Zhao B;Chen S;Liu J;Yuan Z;Qi X;Qin J;Zheng X;Shen X;Yu Y;Qnin TJ;Chan JY;Cai D
Recently, cardiac telocytes were found in the myocardium. However, the functional role of cardiac telocytes and possible changes in the cardiac telocyte population during myocardial infarction in the myocardium are not known. In this study, the role of the recently identified cardiac telocytes in myocardial infarction (MI) was investigated. Cardiac telocytes were distributed longitudinally and within the cross network of the myocardium, which was impaired during MI. Cardiac telocytes in the infarction zone were undetectable from approximately 4 days to 4 weeks after an experimental coronary occlusion was used to induce MI. Although cardiac telocytes in the non‐ischaemic area of the ischaemic heart experienced cell death, the cell density increased approximately 2 weeks after experimental coronary occlusion. The cell density was then maintained at a level similar to that observed 1–4 days after left anterior descending coronary artery (LAD)‐ligation, but was still lower than normal after 2 weeks. We also found that simultaneous transplantation of cardiac telocytes in the infarcted and border zones of the heart decreased the infarction size and improved myocardial function. These data indicate that cardiac telocytes, their secreted factors and microvesicles, and the microenvironment may be structurally and functionally important for maintenance of the physiological integrity of the myocardium. Rebuilding the cardiac telocyte network in the infarcted zone following MI may be beneficial for functional regeneration of the infarcted myocardium.
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影响因子:
5.3
作者:
Cantarero Carmona I;Luesma Bartolomé MJ;Junquera Escribano C
通讯作者:
Junquera Escribano C
影响因子:
5.3
作者:
Kostin S
通讯作者:
Kostin S
影响因子:
5.3
作者:
Manole CG;Cismaşiu V;Gherghiceanu M;Popescu LM
通讯作者:
Popescu LM
影响因子:
5.3
作者:
Faussone-Pellegrini MS;Bani D
通讯作者:
Bani D
影响因子:
11.8
作者:
Leda, Masaki;Tsuchihashi, Takatoshi;Ivey, Kathryn N.;Ross, Robert S.;Hong, Ting-Ting;Shaw, Robin M.;Srivastava, Deepak
通讯作者:
Srivastava, Deepak