Cyclooxygenase COX-2a, a novel COX-2 mRNA variant, in platelets from patients after coronary artery bypass grafting

被引:31
作者
Censarek, P
Freidel, K
Udelhoven, M
Ku, SJ
Hohlfeld, T
Meyer-Kirchrath, J
Schrör, K
Weber, AA
机构
[1] Univ Klinikum Dusseldorf, Inst Pharmakol, D-40225 Dusseldorf, Germany
[2] Univ Klinikum Dusseldorf, Klin Pharmakol, D-40225 Dusseldorf, Germany
关键词
cyclooxygenase-2; splice variant; platelets; coronary artery bypass grafting;
D O I
10.1160/TH04-05-0302
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There are two principal cyclooxygenase isoforms referred to as COX-1 and COX-2. Recently, COX-3 has been identified. We have demonstrated the expression of COX-2 in platelets from patients after coronary artery bypass grafting (CABG). Careful biochemical analysis revealed that, when compared to recombinant COX-2, platelet COX-2 had a slightly higher electrophoretic mobility. Two COX-2 sequences (similar to1.8 kb, similar to1.7 kb) were cloned from platelet mRNA. The similar to1.7 kb sequence, designated COX-2a, differed from the human COX-2 sequence only in, a deletion from position +458 to +567. Similar to the human COX-3, there is a frame shift in the COX-2a sequence resulting in a TAA stop codon at position +490. Thus, the expression of a COX-2a protein corresponding to the 67 kDa COX-2 protein is not clear. However, the marked shifting from COX-2 to COX-2a in platelets from some patients after CABG is a striking finding.
引用
收藏
页码:925 / 928
页数:4
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