Department of Medicine, University of Minnesota Medical School, Minneapolis, MN 55455, USA.
Hepatology. 2012 Feb;55(2):563-74. doi: 10.1002/hep.24712.
Although there have been numerous reports describing the isolation of liver progenitor cells from the adult liver, their exact origin has not been clearly defined; and the role played by mature hepatocytes as direct contributors to the hepatic progenitor cell pool has remained largely unknown. Here, we report strong evidence that mature hepatocytes in culture have the capacity to dedifferentiate into a population of adult liver progenitors without genetic or epigenetic manipulations. By using highly purified mature hepatocytes, which were obtained from untreated, healthy rat liver and labeled with fluorescent dye PKH2, we found that hepatocytes in culture gave rise to a population of PKH2-positive liver progenitor cells. These cells, liver-derived progenitor cells, which share phenotypic similarities with oval cells, were previously reported to be capable of forming mature hepatocytes, both in culture and in animals. Studies done at various time points during the course of dedifferentiation cultures revealed that hepatocytes rapidly transformed into liver progenitors within 1 week through a transient oval cell-like stage. This finding was supported by lineage-tracing studies involving double-transgenic AlbuminCreXRosa26 mice expressing β-galactosidase exclusively in hepatocytes. Cultures set up with hepatocytes obtained from these mice resulted in the generation of β-galactosidase-positive liver progenitor cells, demonstrating that they were a direct dedifferentiation product of mature hepatocytes. Additionally, these progenitors differentiated into hepatocytes in vivo when transplanted into rats that had undergone retrorsine pretreatment and partial hepatectomy.
Our studies provide strong evidence for the unexpected plasticity of mature hepatocytes to dedifferentiate into progenitor cells in culture, and this may potentially have a significant effect on the treatment of liver diseases requiring liver or hepatocyte transplantation.
虽然有大量的报道描述了从成年肝脏中分离肝祖细胞,但它们的确切来源尚未明确;成熟肝细胞作为肝祖细胞池的直接贡献者的作用在很大程度上仍然未知。在这里,我们报告了强有力的证据,证明在没有遗传或表观遗传操作的情况下,培养中的成熟肝细胞具有分化为一群成年肝祖细胞的能力。通过使用从未处理的健康大鼠肝脏中获得的高度纯化的成熟肝细胞,并标记有荧光染料 PKH2,我们发现培养中的肝细胞产生了一群 PKH2 阳性的肝祖细胞。这些细胞,肝源性祖细胞,与卵圆细胞具有相似的表型,以前被报道能够在培养物和动物中形成成熟的肝细胞。在分化培养过程中的各个时间点进行的研究表明,肝细胞在 1 周内通过短暂的卵圆细胞样阶段迅速转化为肝祖细胞。这一发现得到了涉及表达β-半乳糖苷酶的双转基因 AlbuminCreXRosa26 小鼠谱系追踪研究的支持,该酶仅在肝细胞中表达。用从小鼠中获得的肝细胞建立的培养物导致β-半乳糖苷酶阳性的肝祖细胞生成,证明它们是成熟肝细胞的直接去分化产物。此外,当将这些祖细胞移植到接受 retro 丝氨酸预处理和部分肝切除的大鼠体内时,它们会分化为肝细胞。
我们的研究为成熟肝细胞在培养中去分化为祖细胞的意外可塑性提供了有力证据,这可能对需要肝或肝细胞移植治疗的肝脏疾病的治疗产生重大影响。