MAJOR SALIVARY GLANDS OF BOTH HUMANS AND RODENTS CONSIST OF THREE PAIRS OF MACROSCOPIC GLANDS: parotid, submandibular, and sublingual. These glands secrete serous, mucous or mixed saliva via the proper main excretory ducts connecting the glandular bodies with the oral cavity. A series of discoveries about the salivary ducts in the 17th century by Niels Stensen (1638-1686), Thomas Wharton (1614-1673), and Caspar Bartholin (1655-1738) established the concept of exocrine secretion as well as salivary glands. Recent investigations have revealed the endocrine functions of parotin and a variety of cell growth factors produced by salivary glands.The present review aims to describe macroscopic findings on the major salivary glands of rodents and the microscopic differences between those of humans and rodents, which review should be of interest to those researchers studying salivary glands.

Temporal and spatial occurrence of hepatocyte growth factor (HGF) and its cognate receptor c‐Met in the mouse mandibular development was investigated by immunohistochemistry and quantitative reverse transcriptase‐polymerase chain reaction. HGF was first recognized in the mesenchymal cells of the first branchial arch at the 10th day of gestation (E10), before tongue formation, whereas HGF receptor (c‐Met) ‐positive myogenic cells first appeared at E11 in the center of mandibles. By E12, HGF turned to be colocalized with c‐Met in the differentiating tongue myoblasts. Between E14 and E16, HGF disappeared, whereas c‐Met remained, in the tongue myoblasts. The levels of HGF mRNA in the developing tongue decreased in accordance with the increase of desmin mRNA levels from E11 to E17. These in vivo results strongly suggest that the HGF/c‐Met system takes part in the earlier stages of tongue development. To elucidate this hypothesis, the antisense oligodeoxyribonucleotide (A‐ODN) for mouse HGF mRNA was added to the organ culture system of mandible with serumless, defined medium. Mandibular arches from E10 mouse embryos were cultured at 37°C for 10 days in the absence or presence of A‐ODN, control (sense) oligonucleotide (C‐ODN), or A‐ODN plus recombinant HGF. In the control mandibular explants cultured without HGF or ODN, the anterior two‐third of the tongue derived from the first branchial arch was formed. It contained abundant desmin‐positive myoblasts and was equivalent to the tongue of E14–E15. In contrast, in the presence of A‐ODN in the medium, neither the swelling nor myogenic cells were found in the tongue‐forming region of explants, and myogenic cells accumulated behind the tongue‐forming region. Such dysplasia of tongue was never induced in the presence of C‐ODN or A‐ODN plus recombinant HGF in the medium. The effect of A‐ODN appeared to be developmental stage‐specific, because tongue dysplasia occurred when A‐ODN was present during the earlier 4 days but not during the later 4 days of the culture. Furthermore, recombinant HGF added to the culture without ODNs during the earlier 4 days caused elevation in the number of mitotic myoblasts. These results suggest that HGF regulates both the migration and proliferation of myogenic cells during the earlier stages of tongue development.

Immunohistochemical localization of basic fibroblast growth factor (bFGF) was studied in the rat pituitary gland at light and electron microscopic levels using a specific monoclonal antibody. In the anterior lobe, bFGF-immunoreactivity was found mostly in a cell population without secretory granules, which was identified as the folliculo-stellate (FS) cell by its ultra-structure and expression of S-100 protein. The subcellular localization of the immunoreactivity in FS cell was strictly nuclear. Besides the FS cell, a minor cell population containing small granules of 60-100 nm diameter, which seemed to represent immature endocrine cells, was immunostained in the nuclei with the anti-bFGF antibody. In the intermediate lobe, a subpopulation of the S-100 protein-positive cells lining the pituitary cleft was immunoreactive for bFGF. These results imply that the agranular cell types are the main producer and/or target of rat pituitary bFGF, and that bFGF may play a role in the differentiation of pituitary endocrine cells.

Myoepithelial cells (MECs) exist on the basal surface of acini in major exocrine glands, include myofilaments and various constructive proteins, and share characteristics with smooth muscle and epithelial cells. MECs project several ramified processes to invest acini, and possibly contract to compress acini to support the secretion by the glandular cells. However, the functional roles of MECs in salivary secretion are still unclear. We investigated morphological changes in immunostained MECs using the anti-α-smooth muscle actin (αSMA) antibody in operated or non-operated contralateral (NC) submandibular glands after partial or total resection. Furthermore, we investigated and discuss other salivary glands of rats. MECs in the parotid, sublingual and submandibular gland of adult rats exhibited different shapes and localizations. After surgery, in both operated and NC glands, the number of MECs and αSMA-immunopositive areas increased significantly. Three-dimensional analysis using a confocal laser-scanning microscope revealed that substantial and significant enhancement became evident in the number, length, and thickness of MEC-processes covering acini of the operated and NC submandibular glands. The preset findings indicate that MECs alter the morphology of their processes in operated and NC glands after surgery of the partial or total resection. It is suggested that MECs promote salivary secretion using elongated, thickened, and more ramified processes.