Title of article :
Vascular endothelial growth factor mRNA synthesis by peripheral blood mononuclear cells in patients with acute myocardial infarction
Author/Authors :
Yasunobu Sasaki، نويسنده , , Atsuhiko Kawamoto، نويسنده , , Masayuki Iwano، نويسنده , , Hideyuki Kurioka، نويسنده , , Eiji Takase، نويسنده , , Hiroyuki Kawata، نويسنده , , Sota Tsujimura، نويسنده , , Shinya Fukuhara، نويسنده , , Yasuhiro Akai، نويسنده , , Toshio Hashimoto، نويسنده , , Kazuhiro Dohi، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2001
Pages :
10
From page :
51
To page :
60
Abstract :
We studied vascular endothelial growth factor (VEGF) mRNA synthesis by peripheral blood mononuclear cells (PBMCs) in 30 patients with acute myocardial infarction (AMI) and 20 healthy individuals. PBMCs were isolated from all patients on days 3 and 14 after the onset of aMI, and from all of control individuals. To prepare samples containing identical amounts of GAPDH cDNA, competitive PCR was performed by co-amplifying serial dilutions of GAPDH mutant templates. Next, to measure VEGF cDNA quantitatively in the samples containing identical amounts of GAPDH, we also used competitive PCR by co-amplifying mutant templates of VEGF. The serum VEGF concentrations on day 14 in patients with aMI were measured by an ELISA method. Higher levels of VEGF mRNA in PBMCs were present on day 14 than either on day 3 or in the control group. Serum VEGF concentrations correlated with the VEGF mRNA levels of PBMCs on day 14. Peak serum CK levels correlated well with VEGF mRNA levels of PBMCs on day 14. The present findings suggest that PBMCs may be one of the candidates responsible for elevated circulatory VEGF protein following aMI. In addition, VEGF mRNA may be overexpressed in PBMCs in response to cardiac muscle damage.
Keywords :
Acute myocardial infarction , vascular endothelial growth factor , peripheral blood mononuclear cells
Journal title :
International Journal of Cardiology
Serial Year :
2001
Journal title :
International Journal of Cardiology
Record number :
813514
Link To Document :
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