Moran Mary C, Pope Eleanor M, Brewer Matthew G, Beck Lisa A
Department of Dermatology, University of Rochester Medical Center, Rochester, New York, USA.
Department of Microbiology & Immunology, University of Rochester Medical Center, Rochester, New York, USA.
JID Innov. 2022 Nov;2(6):100151. doi: 10.1016/j.xjidi.2022.100151. Epub 2022 Aug 22.
Various culture media are used to propagate keratinocytes (KCs) in vitro. The COVID-19 pandemic resulted in supply chain shortages necessitating substitutions to standard laboratory protocols, which resulted in many laboratories having to use culture media different from those they typically use. We screened available media on the KC line N/TERT2G and found that biological responses varied considerably across three culture media: KC serum-free media, KC growth medium 2, and defined media. We observed qualitative and quantitative differences in proliferation; KCs cultured in defined media had significantly lower proliferative capacity. KC differentiation was assessed by western blot for CLDN1, occludin, cytokeratin-10, and loricrin. Elevated expression of differentiation markers was observed in cells cultured in either KC growth medium 2 or defined media compared with those in cells cultured in KC serum-free media. KC barrier function was measured by transepithelial electrical resistance. KCs cultured in KC growth medium 2 and defined media developed significantly higher transepithelial electrical resistance than those cultured in KC serum-free media, and when treated with IL-4 and IL-13 or IL-17A, we observed variable responses. H&E staining on day 5 -post-differentiation showed greater epithelial thickness in KCs cultured in defined media and KC growth medium 2 than in those cultured in KC serum-free media. These findings show that the choice of culture media impacts the biological response of KCs in a manner that persists through differentiation in the same media.
多种培养基被用于体外培养角质形成细胞(KC)。新冠疫情导致供应链短缺,使得实验室必须对标准实验方案进行调整,这导致许多实验室不得不使用与他们通常使用的不同的培养基。我们在KC细胞系N/TERT2G上筛选了可用的培养基,发现三种培养基(KC无血清培养基、KC生长培养基2和限定培养基)的生物学反应差异很大。我们观察到增殖方面的定性和定量差异;在限定培养基中培养的KC增殖能力显著较低。通过蛋白质免疫印迹法检测CLDN1、闭合蛋白、细胞角蛋白-10和兜甲蛋白来评估KC的分化。与在KC无血清培养基中培养的细胞相比,在KC生长培养基2或限定培养基中培养的细胞中观察到分化标志物的表达升高。通过跨上皮电阻测量KC的屏障功能。在KC生长培养基2和限定培养基中培养的KC比在KC无血清培养基中培养的KC形成了显著更高的跨上皮电阻,并且当用IL-4和IL-13或IL-17A处理时,我们观察到了不同的反应。分化后第5天的苏木精-伊红染色显示,在限定培养基和KC生长培养基2中培养的KC比在KC无血清培养基中培养的KC具有更厚的上皮层。这些发现表明,培养基的选择会以一种在相同培养基中持续分化的方式影响KC的生物学反应。