Department of Tissue Development and Regeneration, Institute of Regenerative Medicine, Sapporo Medical University School of Medicine, Sapporo 060-8556, Japan.
Division of Regenerative Medicine, Center for Stem Cell Biology and Regenerative Medicine, The Institute of Medical Science, The University of Tokyo, Tokyo 108-8639, Japan.
Cells. 2023 Nov 27;12(23):2718. doi: 10.3390/cells12232718.
Mature hepatocytes (MHs) in an adult rodent liver are categorized into the following three subpopulations based on their proliferative capability: type I cells (MH-I), which are committed progenitor cells that possess a high growth capability and basal hepatocytic functions; type II cells (MH-II), which possess a limited proliferative capability; and type III cells (MH-III), which lose the ability to divide (replicative senescence) and reach the final differentiated state. These subpopulations may explain the liver's development and growth after birth. Generally, small-sized hepatocytes emerge in mammal livers. The cells are characterized by being morphologically identical to hepatocytes except for their size, which is substantially smaller than that of ordinary MHs. We initially discovered small hepatocytes (SHs) in the primary culture of rat hepatocytes. We believe that SHs are derived from MH-I and play a role as hepatocytic progenitors to supply MHs. The population of MH-I (SHs) is distributed in the whole lobules, a part of which possesses a self-renewal capability, and decreases with age. Conversely, injured livers of experimental models and clinical cases showed the emergence of SHs. Studies demonstrate the involvement of SHs in liver regeneration. SHs that appeared in the injured livers are not a pure population but a mixture of two distinct origins, MH-derived and hepatic-stem-cell-derived cells. The predominant cell-derived SHs depend on the proliferative capability of the remaining MHs after the injury. This review will focus on the SHs that appeared in the liver and discuss the significance of SHs in liver regeneration.
成熟的肝细胞 (MHs) 在成年啮齿动物肝脏中可根据其增殖能力分为以下三个亚群:I 型细胞 (MH-I),其为具有高生长能力和基础肝细胞功能的定向祖细胞;II 型细胞 (MH-II),其具有有限的增殖能力;以及 III 型细胞 (MH-III),其失去分裂能力(复制衰老)并达到最终分化状态。这些亚群可能解释了肝脏在出生后的发育和生长。通常,小型肝细胞出现在哺乳动物肝脏中。这些细胞除了体积较小外,在形态上与肝细胞完全相同,其体积明显小于普通 MHs。我们最初在大鼠肝细胞的原代培养中发现了小型肝细胞 (SHs)。我们认为 SHs 来源于 MH-I,作为肝细胞祖细胞发挥作用,为 MHs 提供来源。MH-I(SHs)的群体分布在整个小叶中,其中一部分具有自我更新能力,并随着年龄的增长而减少。相反,实验模型和临床病例的受损肝脏中出现了 SHs。研究表明 SHs 参与了肝脏再生。出现在受损肝脏中的 SHs 不是一个纯群体,而是两种不同来源(MH 衍生和肝干细胞衍生)的细胞的混合物。出现的 SHs 主要来源于细胞,取决于损伤后剩余 MHs 的增殖能力。这篇综述将重点介绍出现在肝脏中的 SHs,并讨论 SHs 在肝脏再生中的意义。