Putative cyclooxygenase-3 expression in rat brain cells

被引:68
作者
Kis, B
Snipes, JA
Isse, T
Nagy, T
Busija, DW
机构
[1] Wake Forest Univ, Sch Med, Dept Physiol & Pharmacol, Winston Salem, NC 27157 USA
[2] Univ Occupat & Environm Hlth, Dept Environm Hlth, Kitakyushu, Fukuoka 807, Japan
[3] Univ Szeged, Sch Med, Dept Physiol, Szeged, Hungary
关键词
cyclooxygenase; neuron; astrocyte; cerebral endothelial cell; choroidal epithelial cell; pericyte;
D O I
10.1097/01.WCB.0000090681.07515.81
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cyclooxygenase-3 (COX-3), a new acetaminophen-sensitive isoform of the COX family, has recently been cloned from canine tissues. Canine COX-3 apparently is identical to the full-length form of COX-1, with the exception that the COX-3 mRNA retains intron 1. Additionally, COX-3 mRNA expression is high in the brain. We investigated the expression of the putative rat COX-3 mRNA in primary cultures of neurons, astrocytes, endothelial cells, pericytes, and choroidal epithelial cells from the rat brain. Specific RT-PCR primers were designed to detect putative rat COX-3 mRNA, and the RT-PCR products were sequenced and compared to the known sequence of the rat COX-I gene. Our results demon-strate that the mRNA of the putative COX-3 is expressed in all of the cell types except neurons. Cerebral endothelial cells showed the highest COX-3 expression. Whereas COX-2 expression increased several-fold after lipopolysaccharide (LPS) challenge, COX-I and COX-3 expression did not change significantly, suggesting that cells constitutively express COX-3. In summary, we report, for the first time to our knowledge, that the putative COX-3 mRNA is detectable in rats and is differentially expressed in various cell types from rat brain, as well as that its expression is not stimulated by LPS.
引用
收藏
页码:1287 / 1292
页数:6
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