Clement Jade Q, Lacy Shareen M, Wilson Bobby L
Chemistry Department and NASA University Research Center, Texas Southern University, Houston, Texas, USA.
J Gravit Physiol. 2007 Jul;14(1):P121-2.
Human exposure to microgravity is considered the major environmental factor of space flight that affects cells and tissues causing adverse effects to human health. Ground-based gravity-simulation experiments at the cellular and molecular levels have gained some insight into the underlying molecular and cellular alterations induced by microgravity. However, systematic study and detailed molecular mechanisms of the adverse effect of microgravity on living cells are still lacking. The main objective of this study was to apply DNA microarray technology in time-course experiments for genome-wide search of genes whose expression are altered by microgravity, as part of the effort in the identification of major space genes. In this study, we analyzed global gene expression profiles for a human liver cell line exposed to a ground-based modeled microgravity system for 1, 3, and 4 days using the rotary cell culture system (RCCS) and the Agilent 22k human oligo DNA microarrays. We have found that 139 genes' mRNA levels were significantly (P < or = 0.01) altered by the microgravity exposures. Some of these identified genes were further verified by Northern analysis.
人类暴露于微重力环境被认为是太空飞行的主要环境因素,它会影响细胞和组织,对人类健康造成不利影响。在细胞和分子水平上进行的地面重力模拟实验,已经对微重力诱导的潜在分子和细胞变化有了一些了解。然而,对于微重力对活细胞不利影响的系统研究以及详细分子机制仍然缺乏。本研究的主要目的是在时间进程实验中应用DNA微阵列技术,对全基因组范围内受微重力影响而改变表达的基因进行搜索,作为鉴定主要太空基因工作的一部分。在本研究中,我们使用旋转细胞培养系统(RCCS)和安捷伦22k人类寡核苷酸DNA微阵列,分析了暴露于地面模拟微重力系统1天、3天和4天的人类肝细胞系的全球基因表达谱。我们发现,139个基因的mRNA水平因微重力暴露而发生了显著(P≤0.01)变化。其中一些已鉴定的基因通过Northern分析得到了进一步验证。