Miyazaki T, Fujiki T, Inoue Y, Takano K
Department of Oral Histology, Nagasaki University School of Dentistry, Sakamoto, Japan.
Arch Histol Cytol. 1998 Aug;61(3):199-214. doi: 10.1679/aohc.61.199.
Although human labial gland secretions contain serous components such as the bactericidal enzyme, lysozyme, the presence of serous cells in this gland has yet to be clearly visualized under the electron microscope. The present study identifies lysozyme-expressing cells of the labial glands using microwave-fixed, Epon-Araldite-embedded specimens, which showed excellent preservation of both ultrastructural detail and antigenicity for post-embedding immunogold labeling of lysozyme. Ultrastructurally, all of the secretory cells of the glands appeared to be a mucous-type and have a serial maturation relationship, consistent with a previous report by TANDLER et al. (1969a): their secretory granules were electron-lucent and exhibited reactivity for mucus staining by the periodic acid-thiocarbohydrazide-silver proteinate (PA-TCH-SP) method. We classified them into two immature types (I, II) and two mature types (I, II). Their distinctive features were the following: 1) relatively small (0.5-1 microm) secretory granules and well-developed basal rough endoplasmic reticulum for the immature types; 2) larger (1-2 microm) secretory granules and well-developed Golgi apparatus, which showed intense PA-TCH-SP reactivity in the 2-3 trans-cisterns, for the mature types; 3) few secretory granules in the immature type I; and 4) the darkest appearance for the mature type II. Immunogold labeling with anti-lysozyme showed specific labeling of the two immature-type cells, in which gold particles were found mainly over the secretory granules and Golgi apparatus, and moderately over the rough endoplasmic reticulum. In the secretory granules, the labeling was distributed throughout the contents and was present even if they showed strong PA-TCH-SP reactivity; in the Golgi area, it was seen over the stacked cisternae, trans-Golgi networks, and condensing vacuoles. No specific labeling was seen in the mature-type cells or in the duct cells. These immature- and mature-type cells were almost equivalent to the "serous demilune or acinus" and "mucous tubule" cells, respectively, at the light-microscopic level. These results indicate that the traditional "immature mucous-type cells" of the human labial glands produce lysozyme and should be classified as seromucous cells.
尽管人类唇腺分泌物含有杀菌酶溶菌酶等浆液性成分,但在电子显微镜下该腺体中浆液性细胞的存在尚未得到清晰显现。本研究使用微波固定、环氧树脂-阿拉迪特包埋的标本鉴定唇腺中表达溶菌酶的细胞,这些标本在超微结构细节和溶菌酶包埋后免疫金标记的抗原性方面均保存良好。在超微结构上,腺体的所有分泌细胞似乎均为黏液型,且具有连续的成熟关系,这与坦德勒等人(1969年a)之前的报告一致:它们的分泌颗粒电子密度低,对高碘酸-硫代碳酰肼-银蛋白法(PA-TCH-SP)的黏液染色有反应。我们将它们分为两种未成熟类型(I、II)和两种成熟类型(I、II)。它们的显著特征如下:1)未成熟类型的分泌颗粒相对较小(0.5-1微米),基底粗面内质网发达;2)成熟类型的分泌颗粒较大(1-2微米),高尔基体发达,在2-3个反式扁平囊泡中显示出强烈的PA-TCH-SP反应性;3)未成熟I型中的分泌颗粒较少;4)成熟II型的外观最暗。用抗溶菌酶进行免疫金标记显示两种未成熟类型细胞有特异性标记,其中金颗粒主要见于分泌颗粒和高尔基体,在粗面内质网上也有适度标记。在分泌颗粒中,标记分布于整个内容物中,即使它们显示出强烈的PA-TCH-SP反应性也存在;在高尔基体区域,可见于堆叠的扁平囊泡、反式高尔基体网络和浓缩泡上。在成熟类型细胞或导管细胞中未见特异性标记。在光学显微镜水平上,这些未成熟和成熟类型细胞分别几乎等同于“浆液半月或腺泡”和“黏液小管”细胞。这些结果表明,人类唇腺传统的“未成熟黏液型细胞”产生溶菌酶,应归类为浆液黏液细胞。