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首页> 外文期刊>Journal of cell biology >Expression of hepatic transcription factors during liver development and oval cell differentiation.
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Expression of hepatic transcription factors during liver development and oval cell differentiation.

机译:在肝脏发育和卵圆形细胞分化过程中肝转录因子的表达。

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摘要

The oval cells are thought to be the progeny of a liver stem cell compartment and strong evidence now exists indicating that these cells can participate in liver regeneration by differentiating into different hepatic lineages. To better understand the regulation of this process we have studied the expression of liver-enriched transcriptional factors (HNF1 alpha and HNF1 beta, HNF3 alpha, HNF3 beta, and HNF3 gamma, HNF4, C/EBP, C/EBP beta, and DBP) in an experimental model of oval cell proliferation and differentiation and compared the expression of these factors to that observed during late stages of hepatic ontogenesis. The steady-state mRNA levels of four (HNF1 alpha, HNF3 alpha, HNF4, and C/EBP beta) "liver-enriched" transcriptional factors gradually decrease during the late period of embryonic liver development while three factors (HNF1 beta, HNF3 beta, and DBP) increase. In the normal adult rat liver the expression of all the transcription factors are restricted to the hepatocytes. However, during early stages of oval cell proliferation both small and large bile ducts start to express HNF1 alpha and HNF1 beta, HNF3 gamma, C/EBP, and DBP but not HNF4. At the later stages all of these factors are also highly expressed in the proliferating oval cells. Expression of HNF4 is first observed when the oval cells differentiate morphologically and functionally into hepatocytes and form basophilic foci. At that time the expression of some of the other factors is also further increased. Based on these data we suggest that the upregulation of the "establishment" factors (HNF1 and -3) may be an important step in oval cell activation. The high levels of these factors in the oval cells and embryonic hepatoblasts further substantiates the similarity between the two cell compartments. Furthermore, the data suggest that HNF4 may be responsible for the final commitment of a small portion of the oval cells to differentiate into hepatocytes which form the basophilic foci and eventually regenerate the liver parenchyma.
机译:卵圆形细胞被认为是肝脏干细胞隔室的后代,并且现在存在强有力的证据表明这些细胞可以通过分化为不同的肝谱系而参与肝脏再生。为了更好地了解此过程的调控,我们研究了肝脏富集的转录因子(HNF1 alpha和HNF1 beta,HNF3 alpha,HNF3 beta和HNF3 gamma,HNF4,C / EBP,C / EBP beta和DBP)的表达在卵圆形细胞增殖和分化的实验模型中,将这些因子的表达与肝本体发生后期观察到的表达进行了比较。在胚胎肝发育晚期,四种“肝脏富集”的转录因子的稳态mRNA水平(HNF1 alpha,HNF3 alpha,HNF4和C / EBP beta)逐渐降低,而三种因子(HNF1 beta,HNF3 beta,和DBP)增加。在正常的成年大鼠肝脏中,所有转录因子的表达都局限于肝细胞。但是,在卵圆形细胞增殖的早期,小胆管和大胆管都开始表达HNF1 alpha和HNF1 beta,HNF3γ,C / EBP和DBP,但不表达HNF4。在后期,所有这些因素在增殖的卵圆细胞中也高度表达。当卵圆细胞在形态和功能上分化为肝细胞并形成嗜碱性病灶时,首先观察到HNF4的表达。那时,其他一些因素的表达也进一步增加。基于这些数据,我们建议“建立”因子(HNF1和-3)的上调可能是卵圆细胞激活的重要步骤。卵圆形细胞和胚胎成肝细胞中这些因子的含量较高,进一步证实了两个细胞区室之间的相似性。此外,数据表明HNF4可能负责一小部分卵圆形细胞的最终定型,以分化为形成嗜碱性灶并最终再生肝实质的肝细胞。

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