Müller-Röver S, Handjiski B, van der Veen C, Eichmüller S, Foitzik K, McKay I A, Stenn K S, Paus R
Department of Dermatology, University Hospital Eppendorf, University of Hamburg, Hamburg, Germany.
J Invest Dermatol. 2001 Jul;117(1):3-15. doi: 10.1046/j.0022-202x.2001.01377.x.
Numerous strains of mice with defined mutations display pronounced abnormalities of hair follicle cycling, even in the absence of overt alterations of the skin and hair phenotype; however, in order to recognize even subtle, hair cycle-related abnormalities, it is critically important to be able to determine accurately and classify the major stages of the normal murine hair cycle. In this comprehensive guide, we present pragmatic basic and auxiliary criteria for recognizing key stages of hair follicle growth (anagen), regression (catagen) and quiescence (telogen) in C57BL/6NCrlBR mice, which are largely based on previous work from other authors. For each stage, a schematic drawing and representative micrographs are provided in order to illustrate these criteria. The basic criteria can be employed for all mouse strains and require only routine histochemical techniques. The auxiliary criteria depend on the immunohistochemical analysis of three markers (interleukin-1 receptor type I, transforming growth factor-beta receptor type II, and neural cell-adhesion molecule), which allow a refined analysis of anatomical hair follicle compartments during all hair cycle stages. In contrast to prior staging systems, we suggest dividing anagen III into three distinct substages, based on morphologic differences, onset and progression of melanogenesis, and the position of the dermal papilla in the subcutis. The computer-generated schematic representations of each stage are presented with the aim of standardizing reports on follicular gene and protein expression patterns. This guide should become a useful tool when screening new mouse mutants or mice treated with pharmaceuticals for discrete morphologic abnormalities of hair follicle cycling in a highly reproducible, easily applicable, and quantifiable manner.
许多具有特定突变的小鼠品系表现出明显的毛囊周期异常,即使在皮肤和毛发表型没有明显改变的情况下也是如此;然而,为了识别即使是细微的、与毛发周期相关的异常,能够准确确定并分类正常小鼠毛发周期的主要阶段至关重要。在本综合指南中,我们提出了实用的基本标准和辅助标准,用于识别C57BL/6NCrlBR小鼠毛囊生长(生长期)、退化(退行期)和静止(休止期)的关键阶段,这些标准很大程度上基于其他作者先前的研究成果。对于每个阶段,都提供了示意图和代表性显微照片以说明这些标准。基本标准可用于所有小鼠品系,仅需常规组织化学技术。辅助标准依赖于对三种标志物(白细胞介素-1 I型受体、转化生长因子-β II型受体和神经细胞黏附分子)的免疫组织化学分析,这使得在所有毛发周期阶段都能对毛囊解剖结构进行精细分析。与先前的分期系统不同,我们建议根据形态学差异、黑素生成的起始和进展以及真皮乳头在皮下组织中的位置,将生长期III分为三个不同的亚阶段。呈现每个阶段的计算机生成示意图的目的是使关于毛囊基因和蛋白质表达模式的报告标准化。当以高度可重复、易于应用和可量化的方式筛选新的小鼠突变体或用药物处理的小鼠是否存在毛囊周期的离散形态学异常时,本指南应成为一个有用的工具。