Title of article :
Intracardiac fibroblasts, but not bone marrow derived cells, are the origin of myofibroblasts in myocardial infarct repair
Author/Authors :
Yano، نويسنده , , Toshiyuki and Miura، نويسنده , , Tetsuji and Ikeda، نويسنده , , Yoshihiro and Matsuda، نويسنده , , Eiji and Saito، نويسنده , , Keiji and Miki، نويسنده , , Takayuki and Kobayashi، نويسنده , , Hironori and Nishino، نويسنده , , Yasuhiro and Ohtani، نويسنده , , Seiji and Shimamoto، نويسنده , , Kazuaki، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2005
Pages :
6
From page :
241
To page :
246
Abstract :
Summary of myofibroblasts in infarcted myocardium was examined by using rats in which bone marrow of green fluorescent protein (GFP)-transgenic mice had been transplanted. GFP was not detected in myofibroblasts at either 3 or 7 days after infarction, suggesting that proliferating myofibroblasts in infarcted myocardium are derived from resident fibroblasts rather than circulating precursor cells of bone marrow origin. ound roblasts play important roles in the repair process of myocardial infarct, and their origin has been assumed to be interstitial fibroblasts in the heart. However, bone marrow-derived myofibroblasts have recently been identified in pathological fibrosis in extracardiac tissues. In this study, we aimed to determine whether some of the myofibroblasts in infarcted myocardium are derived from circulating precursor cells of bone marrow origin. s and Results arrow (BM) of GFP-transgenic mice was transplanted into nude rats, and their coronary arteries were occluded for 60 min and reperfused for 3 or 7 days. Non-BM-transplanted rats served as controls. At 3 days after infarction, some endothelial cells were GFP-positive, indicating that they were of bone marrow origin. Predominant cells in infarcted regions were macrophages and neutrophils, and there were only a small number of vimentin-positive cells and fewer myofibroblasts, both of which were GFP-negative. At 7 days after infarction, there were numerous myofibroblasts in granulation tissue replacing necrotic myocytes, and none of them showed GFP signals, whereas some cells were positive for both GFP and vimentin. Appearance of myofibroblasts and extent of the infarct repair in BM-transplanted and those in non-transplanted rats were similar. sions ndings in this study suggest that proliferating myofibroblasts in infarcted myocardium are derived from resident fibroblasts rather than circulating precursor cells of bone marrow origin.
Keywords :
Myofibroblast , Myocardial infarction , Bone marrow , GFP-transgenic mice
Journal title :
Cardiovascular Pathology
Serial Year :
2005
Journal title :
Cardiovascular Pathology
Record number :
1844855
Link To Document :
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