Doi S, Kobayashi M, Sugiura Y, Sakamoto T, Torii S
Department of Pediatrics, Nagoya University School of Medicine, Japan.
Arch Histol Cytol. 1999 Oct;62(4):363-73. doi: 10.1679/aohc.62.363.
To elucidate the detailed kinetics of epidermal Langerhans cells after topical contact sensitizer stimulation, we examined ATPase or Ia positive epidermal cells of BALB/c mice in a time-spaced manner after the topical application of fluorescein isothiocyanate (FITC). We also performed double labeling of Langerhans cells in epidermal sheets with ATPase activity and Ia antigen or costimulatory molecules (B7-1 and B7-2) after the same stimulation. Observations showed that the density of ATPase positive cells and Ia positive cells decreased following a different time course; the former reached a nadir (77.4% of control) at 4 h but the latter reached a minimum (82.8% of control) at 16 h after the application of FITC. A double labeling technique revealed an increase in Ia single positive cells at 4 h as opposed to that of ATPase single positive cells at 16 h after application. Both costimulatory molecules were expressed on the dendritic processes of many Langerhans cells as a dotty pattern at 4 h after application; B7 positive and ATPase negative areas were observed at this time. On electron microscopic observation, a few activated Langerhans cells found in the dermis at 4 h after application had distinctive profiles compared with residual Langerhans cells in the epidermis. These findings suggest that there is a heterogeneity of reactivity to FITC in epidermal Langerhans cells, and that only a small portion of them migrates from the epidermis during sensitization. The findings also indicate the importance of the interaction between the Langerhans cell and its surrounding microenvironment in the epidermis for its activation. In addition, the results indicate that the enzymatic and the phenotypic markers do not definitively reflect the presence (or absence) of Langerhans cells.
为了阐明局部接触致敏剂刺激后表皮朗格汉斯细胞的详细动力学,我们在局部应用异硫氰酸荧光素(FITC)后,以时间间隔的方式检查了BALB/c小鼠的ATP酶或Ia阳性表皮细胞。在相同刺激后,我们还对表皮片中具有ATP酶活性和Ia抗原或共刺激分子(B7-1和B7-2)的朗格汉斯细胞进行了双重标记。观察结果显示,ATP酶阳性细胞和Ia阳性细胞的密度遵循不同的时间进程下降;前者在应用FITC后4小时达到最低点(对照组的77.4%),而后者在16小时达到最小值(对照组的82.8%)。双重标记技术显示,应用后4小时Ia单阳性细胞增加,而16小时ATP酶单阳性细胞增加。两种共刺激分子在应用后4小时以点状模式表达在许多朗格汉斯细胞的树突状突起上;此时观察到B7阳性和ATP酶阴性区域。电子显微镜观察显示,应用后4小时在真皮中发现的少数活化朗格汉斯细胞与表皮中残留的朗格汉斯细胞相比具有独特的形态。这些发现表明,表皮朗格汉斯细胞对FITC的反应存在异质性,并且在致敏过程中只有一小部分细胞从表皮迁移。这些发现还表明,表皮中朗格汉斯细胞与其周围微环境之间的相互作用对其激活很重要。此外,结果表明酶学和表型标记不能明确反映朗格汉斯细胞的存在(或不存在)。