Hirono C, Shiba Y, Kanno Y
Department of Oral Physiology, Hiroshima University School of Dentistry, Japan.
Histochem Cell Biol. 1995 Jan;103(1):39-46. doi: 10.1007/BF01464474.
Antibodies against 21 and 27 kDa gap-junction proteins from rat liver were used to examine the identification and localization of gap-junction proteins in rat salivary glands. Acinar cells of the submandibular glands and parotid glands stained well for the 27 kDa gap junction protein and less intensely for the 21 kDa protein. Acinar cells of the sublingual glands were stained heavily for the 27 kDa gap junction protein and stained well for 21 kDa gap junction protein. No 27 kDa protein was observed in the ducts of the salivary glands. The 21 kDa gap-junction protein was distributed in some of the intercalated ducts in the parotid and submandibular glands. Immunoblotting of an extract of parotid glands with antibodies against 21 and 27 kDa gap-junction proteins revealed the presence of 21 and 27 kDa proteins in the parotid glands. It is concluded that the 27 kDa gap-junction protein is distributed as a major component of the gap junctions in the acinar cells of all the salivary glands; the 21 kDa protein is localized as a minor component in the acinar cells and some portions of the intercalated ducts in the salivary glands. It is possible that these gap-junction proteins might contribute to the regulation of function of the salivary glands.
利用抗大鼠肝脏21 kDa和27 kDa间隙连接蛋白的抗体,检测大鼠唾液腺中间隙连接蛋白的鉴定和定位。下颌下腺和腮腺的腺泡细胞对27 kDa间隙连接蛋白染色良好,对21 kDa蛋白染色较弱。舌下腺的腺泡细胞对27 kDa间隙连接蛋白染色较重,对21 kDa间隙连接蛋白染色良好。在唾液腺导管中未观察到27 kDa蛋白。21 kDa间隙连接蛋白分布在腮腺和下颌下腺的一些闰管中。用抗21 kDa和27 kDa间隙连接蛋白的抗体对腮腺提取物进行免疫印迹分析,结果显示腮腺中存在21 kDa和27 kDa蛋白。得出结论:27 kDa间隙连接蛋白作为所有唾液腺腺泡细胞中间隙连接的主要成分分布;21 kDa蛋白作为次要成分定位于唾液腺腺泡细胞和闰管的某些部分。这些间隙连接蛋白可能有助于调节唾液腺的功能。