Kamide Y, Sasaki H, Abramson M, Huang C C
Department of Otolaryngology, College of Physicians and Surgeons, Columbia University, New York, NY 10032.
Am J Otolaryngol. 1991 Nov-Dec;12(6):307-15. doi: 10.1016/0196-0709(91)90025-b.
Langerhans cells (LCs) are known to play an important role in the immunosurveillance system. In this study, as in others, numerous LCs were detected in the epithelial layer of acquired cholesteatoma by immunohistochemical staining. This finding suggests that cell-mediated immune responses are initiated by LCs in cholesteatoma; however, documentation concerning the microenvironment of LCs-keratinocytes in cholesteatoma is limited. Therefore, we investigated the effects of LCs on keratinocytes in vitro. To study these effects it was necessary to isolate and purify LCs. Our present study revealed that good enrichment and a high degree of purity (95%) of LCs could be obtained from neonatal rat skin using the immunomagnetic beads (Dynabeads M-450) sorting technique. These isolated LCs have the biologic activity of LCs, and Langerhans cells' conditioned medium (LCCM) stimulates DNA synthesis in thymocytes. The effect of LCCM on keratinocytes was then studied. We found that (1) LCCM stimulated DNA synthesis in keratinocytes was then studied. We found that (1) LCCM stimulated DNA synthesis in keratinocytes, but not protein synthesis, and (2) LCCM stimulated the incorporation of 3H-putrescine into keratinocytes by the activation of transglutaminase. Transglutaminase is a known marker of terminal differentiation in keratinocytes. By Western blot analysis, we identified a 17-kd immunoreactive mouse interleukin-1 alpha in LCCM. Our results imply that LCs found in cholesteatoma tissue may play an important role in stimulating both hyper-proliferation and cornification of keratinocytes; two characteristic features of cholesteatoma formation. These stimulatory effects may be due to the release of interleukin-1 or other factors by LCs.
朗格汉斯细胞(LCs)在免疫监视系统中发挥着重要作用。在本研究中,与其他研究一样,通过免疫组化染色在获得性胆脂瘤的上皮层中检测到大量LCs。这一发现表明,胆脂瘤中的细胞介导免疫反应是由LCs启动的;然而,关于胆脂瘤中LCs-角质形成细胞微环境的文献有限。因此,我们在体外研究了LCs对角质形成细胞的影响。为了研究这些影响,有必要分离和纯化LCs。我们目前的研究表明,使用免疫磁珠(Dynabeads M-450)分选技术可以从新生大鼠皮肤中获得良好的富集效果和高纯度(95%)的LCs。这些分离的LCs具有LCs的生物活性,并且朗格汉斯细胞条件培养基(LCCM)可刺激胸腺细胞中的DNA合成。随后研究了LCCM对角质形成细胞的影响。我们发现:(1)LCCM刺激角质形成细胞中的DNA合成,但不刺激蛋白质合成;(2)LCCM通过转谷氨酰胺酶的激活刺激3H-腐胺掺入角质形成细胞。转谷氨酰胺酶是角质形成细胞终末分化的已知标志物。通过蛋白质印迹分析,我们在LCCM中鉴定出一种17-kd的免疫反应性小鼠白细胞介素-1α。我们的结果表明,在胆脂瘤组织中发现的LCs可能在刺激角质形成细胞的过度增殖和角化方面发挥重要作用;这是胆脂瘤形成的两个特征。这些刺激作用可能是由于LCs释放白细胞介素-1或其他因子所致。