Aihara Yasuo, Jahromi Babak S, Yassari Reza, Takahashi Masataka, Macdonald R Loch
Division of Neurosurgery, St. Michael's Hospital, Keenan Research Centre in the Li Ka Shing Knowledge Institute of St. Michael's Hospital, Toronto, Ontario, Canada.
J Neurosci Methods. 2008 Jul 15;172(1):1-7. doi: 10.1016/j.jneumeth.2008.03.020. Epub 2008 Apr 10.
Changes in gene expression are commonly assessed relative to the expression of housekeeping genes, which are assumed to remain unchanged. We tested this assumption in cerebral arteries obtained from dogs 4 and 7 days after subarachnoid hemorrhage (SAH) had been created using the double hemorrhage model. Basilar arteries were removed and examined for expression of messenger ribonucleic acid (mRNA) levels using quantitative real-time polymerase chain reaction. Cross-sections of basilar arteries were stained immunohistochemically for proliferating cell nuclear antigen (PCNA) and 4',6-diamidino-2-phenylindole (DAPI). Positively stained cells were counted and numbers obtained were normalized to the cross-sectional area. The results were compared to normal dog basilar arteries contracted pharmacologically in vitro. SAH resulted in significant vasospasm (P<0.001 for each, paired t-tests). There were significant increases in mRNA for beta-actin (441%, P=0.01), glyceraldehyde-3-phosphate dehydrogenase (566%, P=0.007) and 18S ribosomal RNA (320%, P=0.025) 7 days after SAH. Total mRNA was increased 7 days after SAH relative to genomic DNA (157%, P=0.009). There were significant increases in the number of cells in the tunica media and adventitia of arteries after SAH and a significant decrease in the media after contraction in vitro. Cells in the tunica media and adventitia labeled with PCNA were significantly increased at both times after SAH. Transcripts for housekeeping genes are increased after SAH, making standardization to them potentially invalid. The increase is due to proliferation of cells in the adventitia and increased total mRNA in the media and adventitia.
基因表达的变化通常相对于管家基因的表达进行评估,假定管家基因的表达保持不变。我们使用双次出血模型,在蛛网膜下腔出血(SAH)后4天和7天从犬类获取脑动脉,对这一假设进行了检验。取出基底动脉,使用定量实时聚合酶链反应检测信使核糖核酸(mRNA)水平的表达。基底动脉的横截面进行免疫组织化学染色,以检测增殖细胞核抗原(PCNA)和4',6-二脒基-2-苯基吲哚(DAPI)。对阳性染色细胞进行计数,并将所得数量根据横截面面积进行标准化。将结果与体外经药理学收缩的正常犬基底动脉进行比较。SAH导致显著的血管痉挛(每次配对t检验,P<0.001)。SAH后7天,β-肌动蛋白的mRNA显著增加(441%,P=0.01),甘油醛-3-磷酸脱氢酶的mRNA显著增加(566%,P=0.007),18S核糖体RNA的mRNA显著增加(320%,P=0.025)。SAH后7天,相对于基因组DNA,总mRNA增加(157%,P=0.009)。SAH后,动脉中膜和外膜的细胞数量显著增加,体外收缩后中膜显著减少。SAH后两个时间点,中膜和外膜中标记有PCNA的细胞均显著增加。SAH后管家基因的转录本增加,使其作为标准化的参照可能无效。这种增加是由于外膜细胞增殖以及中膜和外膜中总mRNA增加所致。