Nishioka K, Funato T, Sato Y, Ohta Y, Eto H, Katayama I, Nishiyama S
Department of Dermatology, Kitasato University School of Medicine, Japan.
J Dermatol. 1990 Apr;17(4):205-10. doi: 10.1111/j.1346-8138.1990.tb01627.x.
In order to obtain a good source of human epidermal cell derived thymocyte activating factor (ETAF) for biological study, several cell lines of epidermal origin were cultured. One of the trichilemmoma cell lines, KTL-1, was found to produce ETAF satisfactorily in its culture supernatant. The culture supernatant was collected and analyzed to determine the nature of the ETAF activity. The ETAF activity was completely inhibited by anti-IL 1 alpha antibody, but not by anti-IL 1 beta antibody. Messenger RNA expression by KTL-1 cells was analyzed by using cDNA of IL 1 alpha as a probe. Messenger RNA was not detected in KTL-1 cells by either dot blot analysis or northern blot analysis. However, it was expressed weakly in the cytoplasm by in situ hybridization technique. Messenger RNA expression was easily detected in KTL-1 cells stimulated by lipopolysaccharide (LPS). Messenger RNA expression reached a peak at 3 hours after stimulation of LPS. A trichilemmoma cell line, KTL-1, can be a good source of human ETAF for biological study.
为了获得用于生物学研究的人表皮细胞衍生胸腺细胞活化因子(ETAF)的良好来源,培养了几种表皮来源的细胞系。发现其中一种外毛根鞘瘤细胞系KTL-1在其培养上清液中能令人满意地产生ETAF。收集培养上清液并进行分析以确定ETAF活性的性质。ETAF活性被抗IL-1α抗体完全抑制,但不被抗IL-1β抗体抑制。使用IL-1α的cDNA作为探针分析KTL-1细胞的信使RNA表达。通过斑点印迹分析或Northern印迹分析在KTL-1细胞中均未检测到信使RNA。然而,通过原位杂交技术在细胞质中弱表达。在脂多糖(LPS)刺激的KTL-1细胞中很容易检测到信使RNA表达。在LPS刺激后3小时信使RNA表达达到峰值。外毛根鞘瘤细胞系KTL-1可以作为用于生物学研究的人ETAF的良好来源。