Lee S K, Lim C Y, Chi J G, Yamada K, Hashimura K, Kunikata M, Mori M
Department of Oral Pathology, College of Dentistry, Seoul National University, Korea.
Acta Histochem. 1990;89(2):213-35. doi: 10.1016/S0065-1281(11)80360-0.
The major salivary glands were examined from 69 human fetuses ranging from 10 to 40 weeks of gestation. Prenatal growth curves of developing salivary glands could be established by histological scoring, and development was divided into the early developmental stage (EDS) from 10 to 18 weeks, early intermediate developmental stage (EIDS) from 19 to 24 weeks, late intermediate developmental stage (LIDS) from 15 to 32 weeks, late developmental stage (LDS) from 33 to 40 weeks. Characteristic morphogenesis and cytodifferentiation occurred in glandular duct cells during the period of EIDS and LIDS. In the LDS, acini and ducts of the salivary glands histologically developed into a mature state similar to adult glands. Immunohistochemical staining with monoclonal antibodies (MoAbs) PKK1, KL1, K8.12, K8.13, K4.62, RPN 1160, 1162, 1163, 1164, and 1165 was performed. During the fetal period, keratin expression as revealed by MoAbs PKK1, KL1, K8.12 was well established, and the staining pattern for each of these antibodies was comparable. Other antibodies showed rare or negative staining except K8.13 which had a diffuse, non-specific staining pattern. Accordingly, the proliferation and cytodifferentiation of fetal stage keratin staining in ductal cells as revealed by MoAbs PKK1, KL1, and K8.12 showed a heterogenic distribution in both luminal and basal cells. It is a characteristic finding that the cytodifferentiation of ductal luminal cells precedes ductal basal cells. Ductal basal cells stained with MoAb K8.12 and show heterogeneity of keratin distribution continuously until the full term of gestation. The keratin staining of oral epithelium was also examined to compare with distribution of salivary gland ductal cells and oral epithelial cells. In the present study, the developmental sequence of salivary gland cells and the immunohistochemical properties of keratin proteins in these cells were described in relation to the histogenesis of salivary gland tumours.
对69例孕龄为10至40周的人类胎儿的主要唾液腺进行了检查。通过组织学评分可建立发育中唾液腺的产前生长曲线,发育过程分为10至18周的早期发育阶段(EDS)、19至24周的早期中间发育阶段(EIDS)、25至32周的晚期中间发育阶段(LIDS)、33至40周的晚期发育阶段(LDS)。在EIDS和LIDS期间,腺管细胞发生了特征性的形态发生和细胞分化。在LDS阶段,唾液腺的腺泡和导管在组织学上发育成类似于成人腺体的成熟状态。用单克隆抗体(MoAbs)PKK1、KL1、K8.12、K8.13、K4.62、RPN 1160、1162、1163、1164和1165进行免疫组织化学染色。在胎儿期,MoAbs PKK1、KL1、K8.12所显示的角蛋白表达已确立,且这些抗体各自的染色模式具有可比性。除K8.13具有弥漫性、非特异性染色模式外,其他抗体显示罕见或阴性染色。因此,MoAbs PKK1、KL1和K8.12所显示的胎儿期导管细胞角蛋白染色的增殖和细胞分化在管腔细胞和基底细胞中均呈异质性分布。管腔细胞的细胞分化先于导管基底细胞,这是一个特征性发现。用MoAb K8.12染色的导管基底细胞直至妊娠足月均持续显示角蛋白分布的异质性。还检查了口腔上皮的角蛋白染色,以与唾液腺导管细胞和口腔上皮细胞的分布进行比较。在本研究中,描述了唾液腺细胞的发育序列以及这些细胞中角蛋白的免疫组织化学特性与唾液腺肿瘤组织发生的关系。