Quissell D O, Barzen K A, Deisher L M
University of Colorado Health Sciences Center, School of Dentistry, Department of Basic Sciences and Oral Research, Denver 80262.
Crit Rev Oral Biol Med. 1993;4(3-4):443-8. doi: 10.1177/10454411930040032601.
A series of cAMP analogs that have different specificities for the two different binding sites on the regulatory subunit of type I and type II cAMP-dependent protein kinase (PKA) were used to determine whether selective activation of type I or type II PKA could link either or both isozyme forms of PKA with exocytosis and specific protein phosphorylation in salivary gland cells. Using dispersed rat submandibular or parotid cells, selective activation of either type I or type II resulted in a synergistic response for both rat submandibular mucin and parotid amylase secretion and the phosphorylation of a 26-kDa integral membrane phosphoprotein. These data suggest that the activation of either isozyme of PKA can elicit cellular exocytosis and specific protein phosphorylation in both of these cell types.
一系列对I型和II型环磷酸腺苷(cAMP)依赖性蛋白激酶(PKA)调节亚基上两个不同结合位点具有不同特异性的cAMP类似物,被用于确定I型或II型PKA的选择性激活是否能将PKA的一种或两种同工酶形式与唾液腺细胞中的胞吐作用和特定蛋白质磷酸化联系起来。使用分散的大鼠下颌下腺或腮腺细胞,I型或II型的选择性激活导致大鼠下颌下腺粘蛋白和腮腺淀粉酶分泌以及一种26 kDa整合膜磷蛋白的磷酸化产生协同反应。这些数据表明,PKA的任何一种同工酶的激活都能在这两种细胞类型中引发细胞胞吐作用和特定蛋白质磷酸化。