Dame Michael K, Spahlinger Diana M, DaSilva Marissa, Perone Patricia, Dunstan Robert, Varani James
Department of Pathology, The University of Michigan Medical School, 1150 W. Medical Center Dr., Box 0602, Ann Arbor, MI 48109, USA.
In Vitro Cell Dev Biol Anim. 2008 Jul-Aug;44(7):245-52. doi: 10.1007/s11626-008-9091-3. Epub 2008 Jun 21.
Skin from Gottingen minipigs was used as a source of tissue for organ and cell culture and compared to human skin for growth conditions and sensitivity to irritants. Optimal organ culture conditions were determined, based on the preservation of the histological structure. These included serum-free, growth factor-free conditions with a calcium concentration of 1.5mM. Formulations in which the calcium concentration were low (0.075-0.15mM) failed to support tissue viability (even in the presence of dialyzed serum). Epidermal keratinocytes were grown from tissue explants and as single cells from enzyme-disrupted tissue. Optimal keratinocyte growth was achieved using a serum-free, growth factor-supplemented culture medium with a calcium concentration of 0.15mM. Fibroblasts were optimally grown from explant cultures using a medium with 1.5mM calcium and 10% fetal bovine serum. The conditions that were optimal for maintenance of intact pig skin, as well as for the isolated cells, are the same conditions that have been shown previously to be optimal for intact human skin and skin cells. In additional studies, pig skin keratinocytes and fibroblasts were exposed to a panel of contact irritants and contact sensitizers. Using growth inhibition as the response, the median effective dose values with each agent were very similar to the values previously determined for human epidermal keratinocytes and human dermal fibroblasts. Taken together, these data suggest that the skin from the Gottingen minipig can be used as a surrogate for human skin in ex vivo skin safety studies.
将哥廷根小型猪的皮肤用作器官和细胞培养的组织来源,并与人类皮肤在生长条件和对刺激物的敏感性方面进行比较。基于组织结构的保存确定了最佳的器官培养条件。这些条件包括无血清、无生长因子且钙浓度为1.5mM的条件。钙浓度低(0.075 - 0.15mM)的配方无法维持组织活力(即使存在透析血清)。表皮角质形成细胞从组织外植体生长而来,也可从酶解组织的单细胞生长而来。使用无血清、添加生长因子且钙浓度为0.15mM的培养基可实现角质形成细胞的最佳生长。成纤维细胞使用含有1.5mM钙和10%胎牛血清的培养基从外植体培养物中实现最佳生长。对于完整猪皮肤以及分离细胞维持最佳状态的条件,与先前已证明对完整人类皮肤和皮肤细胞为最佳的条件相同。在额外的研究中,将猪皮肤角质形成细胞和成纤维细胞暴露于一系列接触性刺激物和接触性致敏剂中。以生长抑制作为反应指标,每种试剂的半数有效剂量值与先前针对人类表皮角质形成细胞和人类真皮成纤维细胞测定的值非常相似。综上所述,这些数据表明哥廷根小型猪的皮肤可在体外皮肤安全性研究中用作人类皮肤的替代物。