Autologus bone marrow-derived mesenchymal stem cells intracoronary delivery after acute myocardial infarction in miniature pig.
- Author:
Cheng-qian YIN
1
;
Ji-lin CHEN
;
Yun-fang WANG
;
Feng CAO
;
Rui CHENG
;
Xue-tao PEI
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Female; Male; Mesenchymal Stem Cell Transplantation; methods; Myocardial Infarction; pathology; physiopathology; therapy; Swine; Swine, Miniature; Transplantation, Autologous; Treatment Outcome
- From: Acta Academiae Medicinae Sinicae 2005;27(6):696-699
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo evaluate the possibility that using intracoronary delivery of autologus bone marrow-derived mesenchymal stem cells (MSCs) to improve the cardiac function after acute myocardial infarction (AMI) in miniature pig.
METHODSMSCs were cultured in Dulbecco's modified Eagle's medium-F12 (DMEM/F12) medium. AMI model was made by blocking the blood stream of the first diagonal branch in miniature pig, and released the branch after 90 minutes. After 10-14 days, (4-6) x 10(7) culture-expanded autologus 4', 6-diamidino-2-phenylindole (DAPI)-labelled MSCs were transplanted into each host heart's AMI area through intracoronary way. Ultrasonic cardiography (UCG) was performed to observe the left ventricular function at 3 months after transplantation. The cellular transplanted hearts were harvested and investigated by immunohistochemical analysis.
RESULTSLeft ventricular function of the MSCs group was improved significantly 3 months later compared with the control group [(54.65 +/- 3.39) vs (43.98 +/- 4.21)%, (P < 0.01)]. Exogenous MSCs survived and site-differentiated into cardiomyocytes in infracted hearts.
CONCLUSIONMSCs can play a benificial role to repair damaged heart. Heart function can be improved after MSCs transplantation in porcine myocardial infarction model.