Marchetti L, Gabrielli M G, Materazzi G, Menghi G
Department of Comparative Morphological and Biochemical Sciences, University of Camerino, Italy.
Histol Histopathol. 2000 Apr;15(2):337-46. doi: 10.14670/HH-15.337.
The research was planned to study the subcellular distribution of enzymatic secretory products within the secretory structures of the mouse major salivary glands at light and electron microscopy level by immunogold silver stain (IGSS) technique and double-sided post-embedding immunogold binding and silver amplification in order to speculate about their compartmentation. In particular, we experimented the above immunogold labeling approaches to localize the lysozyme and to verify its distribution patterns in relation to another secretion enzyme, alpha-amylase. Co-presence of lysozyme and alpha-amylase was observed in the convoluted granular tubule cells of the submandibular gland and in the demilunar cells of the sublingual gland as well as in the electron-dense regions of the mottled secretory granules in the parotid gland. Exclusive binding patterns of lysozyme were observed in the acinar cells of the submandibular and sublingual glands where alpha-amylase did not occur.
本研究旨在通过免疫金银染色(IGSS)技术以及双面包埋后免疫金结合和银增强技术,在光学显微镜和电子显微镜水平上研究小鼠主要唾液腺分泌结构内酶分泌产物的亚细胞分布,以便推测其区室化情况。具体而言,我们采用上述免疫金标记方法来定位溶菌酶,并验证其与另一种分泌酶α-淀粉酶相关的分布模式。在下颌下腺的曲折颗粒小管细胞、舌下腺的半月细胞以及腮腺斑驳分泌颗粒的电子致密区域中,观察到溶菌酶和α-淀粉酶共存。在α-淀粉酶不存在的下颌下腺和舌下腺的腺泡细胞中,观察到溶菌酶的特异性结合模式。