Chen Zhongming, Chintagari Narendranath Reddy, Guo Yujie, Bhaskaran Manoj, Chen Jiwang, Gao Li, Jin Nili, Weng Tingting, Liu Lin
Department of Physiological Sciences, Oklahoma State University, 264 McElroy Hall, Stillwater, OK 74078, USA.
Free Radic Biol Med. 2007 Aug 15;43(4):628-42. doi: 10.1016/j.freeradbiomed.2007.05.024. Epub 2007 May 31.
Alveolar epithelial cell (AEC) injury and repair during hyperoxia exposure and recovery have been investigated for decades, but the molecular mechanisms of these processes are not clear. To identify potentially important genes involved in lung injury and repair, we studied the gene expression profiles of isolated AEC II from control, 48-h hyperoxia-exposed (>95% O(2)), and 1-7 day recovering rats using a DNA microarray containing 10,000 genes. Fifty genes showed significant differential expression between two or more time points (P<0.05, fold change >2). These genes can be classified into 8 unique gene expression patterns. Real-time PCR verified 14 selected genes in three patterns related to hyperoxia exposure and early recovery. The change in the protein level for two of the selected genes, bmp-4 and retnla, paralleled that of the mRNA level. Many of these genes were found to be involved in cell proliferation and differentiation. In an in vitro AEC trans-differentiation culture model using AEC II isolated from control and 48-h hyperoxia-exposed rats, the expressions of the cell proliferation and differentiation genes identified above were consistent with their predicted roles in the trans-differentiation of AEC. These data indicate that a coordinated mechanism may control AEC differentiation during in vivo hyperoxia exposure and recovery as well as during in vitro AEC culture.
数十年来,人们一直在研究高氧暴露及恢复过程中肺泡上皮细胞(AEC)的损伤与修复,但这些过程的分子机制尚不清楚。为了鉴定参与肺损伤和修复的潜在重要基因,我们使用包含10000个基因的DNA微阵列,研究了来自对照、高氧暴露48小时(>95% O₂)以及恢复1 - 7天的大鼠的分离肺泡II型上皮细胞(AEC II)的基因表达谱。五十个基因在两个或更多时间点之间表现出显著差异表达(P<0.05,倍数变化>2)。这些基因可分为8种独特的基因表达模式。实时PCR验证了与高氧暴露和早期恢复相关的三种模式中的14个选定基因。所选基因中的两个,即骨形态发生蛋白4(bmp - 4)和视黄醇结合蛋白a(retnla),其蛋白质水平的变化与mRNA水平的变化平行。发现这些基因中的许多都参与细胞增殖和分化。在使用从对照和高氧暴露48小时的大鼠分离的AEC II建立的体外AEC转分化培养模型中,上述鉴定的细胞增殖和分化基因的表达与其在AEC转分化中的预测作用一致。这些数据表明,一种协调机制可能在体内高氧暴露和恢复过程以及体外AEC培养过程中控制AEC分化。