Department of Molecular and Cell Biology, Boston University Henry M. Goldman School of Dental Medicine, Boston, MA, USA.
Methods Mol Biol. 2020;2109:1-22. doi: 10.1007/7651_2019_263.
Although mouse models have been used as an essential tool for studying the physiology and diseases of the skin, propagation of mouse primary epidermal keratinocytes remains challenging. In this chapter, we introduce the simplest, at least to our knowledge, protocol that enables long-term expansion of p63 mouse epidermal keratinocytes in low Ca media without the need of progenitor cell-purification steps or support by a feeder cell layer. Pharmacological inhibition of TGF-β signaling in crude preparations of mouse epidermis robustly increases proliferative capacity of p63 epidermal progenitor cells, while preserving their ability to differentiate. Suppression of TGF-β signaling also permits p63 epidermal keratinocytes to form macroscopically large clones in 3T3-J2 feeder cell co-culture. Suppression of TGF-β signaling also enhances the clonal growth of human keratinocytes in co-culture with a variety of feeder cells. This simple and efficient approach will not only facilitate the use of mouse models by providing p63 primary epidermal keratinocytes in quantity but also significantly reduce the time needed for preparing the customized skin grafts in Green method.
虽然小鼠模型已被广泛应用于研究皮肤的生理学和疾病,但原代小鼠表皮角质形成细胞的培养仍然具有挑战性。在本章中,我们介绍了一种最简单的方法,据我们所知,该方法能够在低钙培养基中长时间扩增 p63 小鼠表皮角质形成细胞,而无需进行祖细胞纯化步骤或饲养细胞层的支持。在粗制的小鼠表皮制剂中,抑制 TGF-β 信号通路可显著增强 p63 表皮祖细胞的增殖能力,同时保持其分化能力。抑制 TGF-β 信号通路还允许 p63 表皮角质形成细胞在 3T3-J2 饲养细胞共培养中形成肉眼可见的大克隆。抑制 TGF-β 信号通路还可增强与多种饲养细胞共培养的人角质形成细胞的克隆生长。这种简单而高效的方法不仅可以通过提供大量的 p63 原代表皮角质形成细胞来促进小鼠模型的应用,还可以显著缩短 Green 方法中定制皮肤移植物的制备时间。