Naito Yuji, Mizushima Katsura, Yoshikawa Toshikazu
Molecular Gastroenterology and Hepatology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, Japan.
Dig Dis Sci. 2005 Oct;50 Suppl 1:S45-55. doi: 10.1007/s10620-005-2806-3.
Gastric ischemia-reperfusion is a relatively common condition leading to mucosal injury and may affect mucosal repair via modulating the gene expression of growth factors. Therefore, precise understanding of the molecular mechanism of ischemia or ischemia-reperfusion may lead to the discovery of new mucosal protective drugs. DNA microarray analysis followed by powerful data analysis has the potential to uncover previously undescribed genes involved in gastric injury and lead to an increased understanding of gastric mucosal cytoprotection. We introduced the laser-assisted microdissection to obtain cell-specific RNA from gastric mucosa in vivo and obtained sufficient amounts of cRNA for GeneChip analysis. This comprehensive approach enabled the simultaneous analysis of many genes, including transcriptional factors, as well as the generation of novel hypothesis on the mechanism of action of gastro-protective agents.
胃缺血再灌注是导致黏膜损伤的一种相对常见的病症,并且可能通过调节生长因子的基因表达来影响黏膜修复。因此,精确了解缺血或缺血再灌注的分子机制可能会促成新型黏膜保护药物的发现。DNA微阵列分析结合强大的数据分析有潜力揭示此前未被描述的参与胃损伤的基因,并增进对胃黏膜细胞保护作用的理解。我们引入激光辅助显微切割技术以在体内从胃黏膜获取细胞特异性RNA,并获得了足够量的用于基因芯片分析的cRNA。这种综合方法能够同时分析包括转录因子在内的许多基因,并能就胃保护剂的作用机制生成新的假设。