肿瘤抑制基因Klf6在ES细胞分化中的不同作用

N. Matsumoto, N. Matsumoto, Xiao Zhao, F. Itoh, S. Friedman
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引用次数: 3

摘要

Klf6是一种锌指转录因子,已被确定为几种人类癌症中失活的肿瘤抑制基因。我们之前报道过,由于造血分化受损,Klf6-/-小鼠是胚胎致死的。在该研究中,我们还发现Klf6-/-小鼠的肝脏无法确定。结合这一观察结果及其发育表达模式,Klf6可能在非造血组织分化中发挥作用。本研究的目的是利用组织特异性胚胎干细胞分化系统更清楚地定义Klf6在组织分化中的作用。我们评估了三种不同的培养条件诱导ES细胞分化,比较了Klf6+/+和Klf6-/- ES细胞的反应。Klf6-/- ES细胞的神经元分化受到标记基因表达和形态学的影响。有趣的是,Klf6 -/- ES细胞开始表达Hnf3β mRNA,这表明这些细胞是内胚层前体细胞,这表明在这种培养条件下Klf6通常抑制内胚层分化。此外,当Klf6-/- ES细胞在StemPro34无血清培养基中生长时,它们比Klf6+/+ ES细胞表现出更大程度的心脏分化,这表明Klf6可能具有阻止心肌发生的抑制活性。这些发现表明Klf6在胚胎干细胞分化中具有不同的组织特异性作用。
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Divergent roles of tumor suppressor gene Klf6 in ES cell differentiation
Klf6 is a zinc finger transcription factor that has been identified as a tumor suppressor gene inactivated in several human cancers. We previously reported that Klf6-/- mice are embryonic lethal because of impaired hematopoietic differentiation. In that study, we also found Klf6-/- mice have undefinable livers. Combined with this observation and its developmental expression pattern, Klf6 might have a role in in differentiation of non-hematopoietictissues. The aim of this study was to more clearly define the roles of Klf6 in tissue specification using tissue-specific ES cell differentiation systems. We have evaluated three different culture conditions to induce ES cell differentiation, comparing the responses between Klf6+/+ and Klf6-/- ES cells. Neuronal differentiation of Klf6-/- ES cells was impaired based on marker gene expression and morphology. Interestingly, Klf6 -/- ES cells began to express Hnf3β mRNA, which identified these cells as endodermal precursors, suggesting that Klf6 ordinarily suppresses endoderm differentiation in this culture condition. Additionally, when Klf6-/- ES cells were grown in StemPro34 serum free medium, they showed enhanced cardiac differentiation to a greater extent than Klf6+/+ ES cells, suggesting that Klf6 may have an inhibitory activity in preventing cardiomyogenesis. These findings indicate divergent and tissue- specific roles of Klf6 in ES cell differentiation.
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