Immunocytochemical analysis of cyclic AMP receptor proteins in the developing rat parotid gland

被引:5
作者
Mednieks, Maija [2 ]
Lin, Marcus [1 ]
Hand, Arthur R. [2 ]
机构
[1] Meharry Med Coll, Sch Dent, Nashville, TN 37208 USA
[2] Univ Connecticut, Sch Dent Med, Dept Oral Hlth & Diagnost Sci, Ctr Hlth, Farmington, CT 06030 USA
关键词
parotid; development; morphology; secretion; cyclic AMP; PKA-RII;
D O I
10.1016/j.archoralbio.2007.11.012
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Previous studies showed that regulatory subunits of type II cyclic AMP-dependent protein kinase (RII) are present in adult rat parotid acinar cells, and are secreted into saliva. If the synthesis and intracellular distribution of RII exhibit developmental specificity, then RII call be an indicator of secretory and regulatory activity of salivary glands. Objective: To determine the expression and distribution of RII in the rat parotid at specific ages representing defined developmental stages. Methods: Parotid glands of fetal, neonatal and adult rats were prepared for morphologic and immunocytochemical study. The cellular distribution of RII was studied using light microscopic immunogold silver staining with anti-RII, and its intracellular distribution using electron microscopic immunogold labeling. Results: In utero, parotid RE levels were low; 5-18 days after birth, labeling of secretory granules and cytoplasm rose to a peak, followed by a rapid decrease in both compartments at 25 days. At 60 days, granule labeling increased to levels near those at 18 days, whereas cytoplasmic labeling remained low. Nuclear labeling was highest during the first 3 weeks after birth, and then declined. Conclusions: The higher nuclear and cytoplasmic labeling during the neonatal period may reflect RII involvement in acinar cell differentiation. The accumulation of RII in secretory granules is similar to the pattern of the major salivary proteins, amylase and PSP. The redistribution of RII in these compartments during development may reflect changing gene expression patterns, and may be useful for identification of genetic or metabolic abnormalities. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:429 / 436
页数:8
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