Increased expression of phospholipase D in the heart with experimental autoimmune myocarditis in Lewis rats

被引:7
作者
Ahn, M
Lee, Y
Sim, KB
Min, DS
Matsumoto, Y
Wie, MB
Shin, YG
Shin, T [1 ]
机构
[1] Jeju Natl Univ, Coll Agr & Life Sci, Dept Vet Med, Jeju 690756, South Korea
[2] Jeju Natl Univ, Coll Med, Dept Neurosurg, Jeju 690756, South Korea
[3] Catholic Univ Korea, Coll Med, Dept Physiol, Seoul, South Korea
[4] Tokyo Metropolitan Inst Neurosci, Dept Mol Neuropathol, Tokyo, Japan
[5] Kangwon Natl Univ, Dept Vet Med, Chunchon, South Korea
[6] Daegu Polytech Coll, Taegu, South Korea
关键词
experimental autoimmune myocarditis; phospholipase D; proliferation; cardiomyocytes;
D O I
10.1081/IMM-120027688
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The expression of phospholipase D (PLD) in the hearts of rats with experimental autoimmune myocarditis (EAM) was studied to elucidate the functional role of PLD in the pathogenesis of EAM. Western blot analysis showed that the level of the PLD1 isoform was significantly increased in the hearts of rats with EAM on days 14, 17 and 21 postimmunization (pi) (P < 0.01; control vs EAM at 14 pi, 17 pi and 21 pi). The phenotypes of cells exhibiting increased PLD1 expression were primarily inflammatory cells, including ED1 positive macrophages, in the inflammatory EAM lesions. Some cardiomyocytes also showed increased PLD1 immunoreaction in and around EAM lesions. Some PLD1-positive cells were also positive for proliferating cell nuclear antigen in some cardiomyocytes or terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick end-labeling in some macrophages, suggesting that PLD1 positive cells have a capacity for proliferation or apoptosis depending on cell types in the target organ. Thus, it is postulated that increased expression of PLD1 in EAM may support an early inflammatory response in proliferating inflammatory cells, and its expression in cardiomyocytes may help them to survive by activation of survival factors in hearts with EAM.
引用
收藏
页码:95 / 105
页数:11
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