Kimlin Lauren, Virador Victoria
NIH, Bethesda, MD, USA.
Methods Mol Biol. 2013;989:217-33. doi: 10.1007/978-1-62703-330-5_17.
We developed protocols for isolation and characterization of mesenchymal progenitors from murine dermis. Our protocols are part of a more general isolation procedure starting with neonatal murine skin, which has been described in detail by U. Lichti and coauthors (Nat Protoc 3(5):799-810, 2008). We list Lichti's procedures in an abbreviated form as part of this methods section. Our methods to isolate mesenchymal stem cells are presented as a continuous workflow of isolation and characterization, including flow cytometry, cell survival assays, colony formation assays, immunoblotting, immunostaining, multipotential differentiation assays, and in vivo engraftment. In most cases, the protocols are standard; in others, they were adapted to our particular purpose. We made special emphasis on the use of in vitro three-dimensional cultures to cue mesenchymal progenitors into epidermal cells.
我们开发了从小鼠真皮中分离和鉴定间充质祖细胞的方案。我们的方案是从新生小鼠皮肤开始的更通用分离程序的一部分,U. Lichti及其合著者已对此进行了详细描述(《自然方法》3(5):799 - 810, 2008)。作为本方法部分的一部分,我们以简略形式列出了Lichti的程序。我们分离间充质干细胞的方法呈现为分离和鉴定的连续工作流程,包括流式细胞术、细胞存活测定、集落形成测定、免疫印迹、免疫染色、多能分化测定和体内植入。在大多数情况下,方案是标准的;在其他情况下,它们是根据我们的特定目的进行调整的。我们特别强调使用体外三维培养来促使间充质祖细胞分化为表皮细胞。