Richter Karin, Wirta Valtteri, Dahl Lina, Bruce Sara, Lundeberg Joakim, Carlsson Leif, Williams Cecilia
Umeå Center for Molecular Medicin, Umeå Universitet, 90187 Umeå, Sweden.
BMC Genomics. 2006 Apr 6;7:75. doi: 10.1186/1471-2164-7-75.
Expression of the LIM-homeobox gene Lhx2 in murine hematopoietic cells allows for the generation of hematopoietic stem cell (HSC)-like cell lines. To address the molecular basis of Lhx2 function, we generated HSC-like cell lines where Lhx2 expression is regulated by a tet-on system and hence dependent on the presence of doxycyclin (dox). These cell lines efficiently down-regulate Lhx2 expression upon dox withdrawal leading to a rapid differentiation into various myeloid cell types.
Global gene expression of these cell lines cultured in dox was compared to different time points after dox withdrawal using microarray technology. We identified 267 differentially expressed genes. The majority of the genes overlapping with HSC-specific databases were those down-regulated after turning off Lhx2 expression and a majority of the genes overlapping with those defined as late progenitor-specific genes were the up-regulated genes, suggesting that these cell lines represent a relevant model system for normal HSCs also at the level of global gene expression. Moreover, in situ hybridisations of several genes down-regulated after dox withdrawal showed overlapping expression patterns with Lhx2 in various tissues during embryonic development.
Global gene expression analysis of HSC-like cell lines with inducible Lhx2 expression has identified genes putatively linked to self-renewal/differentiation of HSCs, and function of Lhx2 in organ development and stem/progenitor cells of non-hematopoietic origin.
LIM 同源框基因 Lhx2 在小鼠造血细胞中的表达能够产生造血干细胞(HSC)样细胞系。为了探究 Lhx2 功能的分子基础,我们构建了 HSC 样细胞系,其中 Lhx2 的表达受四环素诱导系统调控,因此依赖强力霉素(dox)的存在。这些细胞系在撤除 dox 后能有效下调 Lhx2 的表达,从而迅速分化为多种髓系细胞类型。
利用微阵列技术,将在 dox 中培养的这些细胞系的全局基因表达与撤除 dox 后的不同时间点进行了比较。我们鉴定出 267 个差异表达基因。与 HSC 特异性数据库重叠的大多数基因是在关闭 Lhx2 表达后下调的基因,而与定义为晚期祖细胞特异性基因重叠的大多数基因是上调基因,这表明这些细胞系在全局基因表达水平上也代表了正常 HSC 的相关模型系统。此外,对撤除 dox 后下调的几个基因进行原位杂交显示,在胚胎发育过程中,它们在各种组织中的表达模式与 Lhx2 重叠。
对具有可诱导 Lhx2 表达的 HSC 样细胞系进行全局基因表达分析,已鉴定出可能与 HSC 的自我更新/分化以及 Lhx2 在器官发育和非造血来源的干/祖细胞中的功能相关的基因。