Strachan Lauren R, Ghadially Ruby
Department of Dermatology, University of California San Francisco, San Francisco, CA 94143, USA.
Stem Cell Rev. 2008 Sep;4(3):149-57. doi: 10.1007/s12015-008-9020-6.
As one of the most proliferative tissues in adult mammals, the epidermis is a good example of the precise regulation necessary between stem cell self-renewal and differentiation. The epidermis is derived from ectodermal progenitor cells and contains three distinct classes of cells: epidermal stem cells which are capable of infinite rounds of cell division; their immediate descendants, transient amplifying cells, which are capable of numerous but finite rounds of cell division; and finally, non-dividing, differentiating cells (Aberdam in Cell and Tissue Research 331:103-107, 2008). This proliferative hierarchy must be tightly regulated both temporally and spatially during epidermal development and homeostasis in order to prevent uncontrolled growth leading to hyperproliferative states and/or tumorigenesis. Historically, the most basic unit of epidermal proliferation has been described as the epidermal proliferation unit (EPU). The EPU, as originally characterized by Christophers, Potten and Mackenzie, is a proliferation unit consisting of approximately 10 basal cells with a clonogenic cell in the center and overlaid by the suprabasal and corneocyte progeny (reviewed in Potten, C. S. (1974). The epidermal proliferative unit: the possible role of the central basal cell. Cell and Tissue Kinetics, 7(1), 77-88). Numerous researchers have identified this classical EPU structure, consisting of approximately 20 cells, in a variety of mammalian skin sources. Recently however, lineage analyses have provided evidence for much larger clonal epidermal units consisting of hundreds to thousands of cells. Furthermore, cutaneous mosaicism as well as a variety of cutaneous pathologies indicate that clonal areas extend to whole patches of mammalian skin many centimeters across. In this review we revisit four decades of experimental evidence and put forward a model of clonal units derived from multiple classes of epidermal progenitors ranging from the largest and most primitive units, clonal ectodermal units, to epidermal stem cell units, and finally, to the most basic structural unit, the EPU.
作为成年哺乳动物中增殖能力最强的组织之一,表皮是干细胞自我更新与分化之间精确调控的一个典型例子。表皮源自外胚层祖细胞,包含三类不同的细胞:能够进行无限轮细胞分裂的表皮干细胞;其直接后代,即短暂扩增细胞,能够进行多次但有限轮的细胞分裂;最后是不再分裂、正在分化的细胞(阿贝丹姆,《细胞与组织研究》331:103 - 107,2008年)。在表皮发育和稳态维持过程中,这种增殖层次结构必须在时间和空间上受到严格调控,以防止不受控制的生长导致过度增殖状态和/或肿瘤发生。从历史上看,表皮增殖的最基本单位被描述为表皮增殖单位(EPU)。EPU最初由克里斯托弗斯、波顿和麦肯齐所描述,是一个增殖单位,由大约10个基底细胞组成,中心有一个克隆形成细胞,并被基底上层和角质形成细胞后代覆盖(波顿,C.S.(1974年)。表皮增殖单位:中央基底细胞可能的作用。《细胞与组织动力学》,7(1),77 - 88)。众多研究人员在多种哺乳动物皮肤来源中都鉴定出了这种由大约20个细胞组成的经典EPU结构。然而最近,谱系分析提供了证据,表明存在由数百到数千个细胞组成的大得多的克隆表皮单位。此外,皮肤镶嵌现象以及多种皮肤病理学表明,克隆区域可延伸至横跨数厘米的整个哺乳动物皮肤斑块。在本综述中,我们回顾了四十年来的实验证据,并提出了一个克隆单位模型,该模型源自多类表皮祖细胞,从最大、最原始的单位,即克隆外胚层单位,到表皮干细胞单位,最后到最基本的结构单位,即EPU。