Wagner Wolfgang, Saffrich Rainer, Wirkner Ute, Eckstein Volker, Blake Jonathon, Ansorge Alexandra, Schwager Christian, Wein Frederik, Miesala Katrin, Ansorge Wilhelm, Ho Anthony D
Department of Medicine V, University of Heidelberg, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany.
Stem Cells. 2005 Sep;23(8):1180-91. doi: 10.1634/stemcells.2004-0361. Epub 2005 Jun 13.
Cell-cell contact between stem cells and cellular determinants of the microenvironment plays an essential role in controlling cell division. Using human hematopoietic progenitor cells (CD34+/CD38-) and a stroma cell line (AFT024) as a model, we have studied the initial behavioral and molecular sequel of this interaction. Time-lapse microscopy showed that CD34+/CD38- cells actively migrated toward and sought contact with stroma cells and 30% of them adhered firmly to AFT024 stroma through the uropod. CD44 and CD34 are colocalized at the site of contact. Gene expression profiles of CD34+/CD38- cells upon cultivation with or without stroma for 16, 20, 48, or 72 hours were analyzed using our human genome cDNA microarray. Chk1, egr1, and cxcl2 were among the first genes upregulated within 16 hours. Genes with the highest upregulation throughout the time course included tubulin genes, ezrin, c1qr1, fos, pcna, mcm6, ung, and dnmt1, genes that play an essential role in reorganization of the cytoskeleton system, stabilization of DNA, and methylation patterns. Our results demonstrate directed migration of CD34+/CD38- cells toward AFT024 and adhesion through the uropod and that upon interaction with supportive stroma, reorganization of the cytoskeleton system, regulation of cell division, and maintenance of genetic stability represent the most essential steps.
干细胞与微环境的细胞决定因素之间的细胞间接触在控制细胞分裂中起着至关重要的作用。我们以人类造血祖细胞(CD34+/CD38-)和一种基质细胞系(AFT024)为模型,研究了这种相互作用的初始行为和分子后续变化。延时显微镜观察显示,CD34+/CD38-细胞积极向基质细胞迁移并寻求接触,其中30%的细胞通过尾足与AFT024基质牢固黏附。CD44和CD34在接触部位共定位。使用我们的人类基因组cDNA微阵列分析了CD34+/CD38-细胞在有或无基质的情况下培养16、20、48或72小时后的基因表达谱。Chk1、egr1和cxcl2是在16小时内最早上调的基因之一。在整个时间进程中上调程度最高的基因包括微管蛋白基因、埃兹蛋白、c1qr1、fos、增殖细胞核抗原、微小染色体维持蛋白6、尿嘧啶-DNA糖基化酶和DNA甲基转移酶1,这些基因在细胞骨架系统重组、DNA稳定和甲基化模式中起着至关重要的作用。我们的结果表明,CD34+/CD38-细胞向AFT024定向迁移并通过尾足黏附,并且与支持性基质相互作用时,细胞骨架系统的重组、细胞分裂的调节和遗传稳定性的维持是最关键的步骤。