Roussa E, Thévenod F
Dept. Anatomy, University of the Saarland, Homburg/Saar, Germany.
Eur J Morphol. 1998 Aug;36 Suppl:147-52.
Using immunohistochemistry we have investigated the presence and cellular distribution of the 31-kDa subunit of vacuolar-type H+-ATPase (V-ATPase) in secretory endpieces and the duct system of rat major salivary glands. In all three salivary glands studied the 31-kDa subunit of V-ATPase was not expressed in secretory endpieces. In rat parotid gland V-ATPase was luminally located in main excretory and striated duct cells. In contrast, both rat submandibular and sublingual glands showed a diffuse intracellular V-ATPase distribution. The differences in V-ATPase immunolocalization in rat salivary glands probably reflect the structural heterogeneity of the different glands. The data also suggest that the duct systems of major salivary glands may modify the H+ and HCO3- concentration of the final saliva in different ways.
我们运用免疫组织化学方法,研究了液泡型H⁺-ATP酶(V-ATP酶)31-kDa亚基在大鼠主要唾液腺分泌末端和导管系统中的存在情况及细胞分布。在所研究的所有三种唾液腺中,V-ATP酶的31-kDa亚基在分泌末端均未表达。在大鼠腮腺中,V-ATP酶位于主排泄管和纹状管细胞的管腔面。相比之下,大鼠下颌下腺和舌下腺的V-ATP酶在细胞内呈弥漫性分布。大鼠唾液腺中V-ATP酶免疫定位的差异可能反映了不同腺体的结构异质性。这些数据还表明,主要唾液腺的导管系统可能以不同方式调节最终唾液的H⁺和HCO₃⁻浓度。