Gene proriling changes in cytoskeletal proteins during clinical recovery after left ventricular-assist device support

被引:80
作者
Birks, EJ
Hall, JL
Barton, PJR
Grindle, S
Latif, N
Hardy, JP
Rider, JE
Banner, NR
Khaghani, A
Miller, LW
Yacoub, MH [1 ]
机构
[1] Royal Brompton & Harefield Hosp, Heart Sci Ctr, Harefield UB9 6JH, Middx, England
[2] Univ London Imperial Coll Sci Technol & Med, Natl Heart & Lung Inst, Heart Sci Ctr, London SW7 2AZ, England
[3] Univ Minnesota, Dept Med, Div Cardiovasc, Minneapolis, MN 55455 USA
关键词
heart failure; heart-assist device; myocardial contraction; remodeling; genes;
D O I
10.1161/CIRCULATIONAHA.104.526137
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-After left ventricular-assist device (LVAD) support, a proportion of patients recover sufficient ventricular function to enable explantation of the device. The exact molecular mechanisms involved in myocardial recovery remain unknown. Cytoskeletal proteins are essential for the structure and function of the cardiac myocyte and might play a major role. Methods and Results-A total of 15 patients with nonischemic cardiomyopathy who required LVAD implantation were studied; 6 recovered sufficiently to allow explantation of the device compared with 9 who did not recover and required transplantation. LV myocardial samples were collected at implantation and explantation/transplantation. Affymetrix microarray analysis was performed on the paired samples and analyzed with reference to sarcomeric and nonsarcomeric cytoskeletal proteins. In the recovery group, of the nonsarcomeric proteins, lamin A/C increased 1.5-fold (P < 0.05) and spectrin 1.6-fold (P < 0.05) between the times of implantation and explantation. Integrins beta 1, beta 6, and alpha 7 decreased 1.7-fold (P < 0.05), 2.4-fold (P < 0.05), and 1.5-fold (P < 0.05), respectively, but integrins alpha 5 and beta 5 increased 2.3-fold (P < 0.01) and 1.2-fold (P < 0.01) at explantation. The following sarcomeric proteins changed in the recovered group only: beta-actin increased 1.4-fold (P < 0.05); a-tropomyosin, 1.3-fold (P < 0.05); alpha 1-actinin, 1.8-fold (P < 0.01); and alpha-filarnin A, 1.6-fold (P < 0.05). Both troponin T3 and alpha 2-actinin decreased by 1.6-fold at the time of explantation (P<0.05). Vinculin decreased 1.7-fold (P=0.001) in the recovered group but increased by 1.7-fold (P<0.05) in the nonrecovered group. Vinculin protein levels decreased 4.1-fold in the recovered group. Conclusions-Myocardial recovery was associated with a specific pattern of changes in sarcomeric, nonsarcomeric, and membrane-associated proteins, which could have important implications in understanding the mechanisms involved.
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收藏
页码:I57 / I64
页数:8
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