Morris Rebecca J, Readio Nyssa, Boland Kelsey, Johnson Kelly, Lad Sonali, Singh Anupama, Singh Ashok, Holtorf Stephanie, Skaar Samantha
Hormel Institute, University of Minnesota;
Hormel Institute, University of Minnesota.
J Vis Exp. 2019 Aug 10(150). doi: 10.3791/58701.
The protocol described here is a reliable method of harvesting primary keratinocytes from adult female mice (54 ± 2 days old) yielding approximately 30 x 10 viable cells per mouse. Primary adult mouse keratinocytes are harvested from the dorsal skin of female mice. Male mice (~6 weeks old) can be used for keratinocyte harvesting depending on the requirements of the experiment. Euthanized mice are shaved and sterilized with serial washes in povidone iodine and ethanol solutions (70% alcohol). After disinfecting the mice, the dorsal skin is removed and the subcutaneous fat and muscle are removed with a scalpel and discarded. The skins are cut into small pieces and treated with a mild, low temperature trypsinization to detach the lower dermis from the epidermis. The scraped epidermises are stirred at low speed, filtered to remove the hairs, counted, and re-suspended in culture medium. This method provides an excellent single cell suspension of highly culturable cells for many downstream applications.
此处描述的方案是一种从成年雌性小鼠(54±2日龄)获取原代角质形成细胞的可靠方法,每只小鼠可获得约30×10个活细胞。成年小鼠原代角质形成细胞从雌性小鼠的背部皮肤获取。根据实验要求,雄性小鼠(约6周龄)也可用于角质形成细胞的获取。对安乐死的小鼠进行剃毛处理,并用聚维酮碘和乙醇溶液(70%酒精)连续冲洗进行消毒。对小鼠进行消毒后,切除背部皮肤,并用手术刀去除皮下脂肪和肌肉,然后丢弃。将皮肤切成小块,用温和的低温胰蛋白酶消化处理,以使真皮下层与表皮分离。刮下的表皮以低速搅拌,过滤以去除毛发,计数后重新悬浮于培养基中。该方法可为许多下游应用提供优良的、高度可培养的单细胞悬液。