By removing connective tissue components with enzymatic digestion followed by HCl-hydrolysis, myoepithelial cells (MECs) of the terminal portion in a variety of exocrine glands of the rat were examined with the scanning electron microscope. The profile of MECs varied considerably from gland to gland; MECs in the lactating mammary gland have a few long cytoplasmic processes in close contact with those of adjacent cells forming a continuous network around the terminal portion. Those of the exorbital lacrimal gland are stellate with many thin radiating processes with tapered ends that terminate freely. MECs in the sublingual gland are characterized by a number of broad and extensive cellular processes. MECs in the submandibular gland are similar in appearance to those of the exorbital lacrimal gland, but with more extensive cellular processes that form a more or less continuous network with those of the adjacent cells. No MECs were observed on the terminal portion of the parotid gland where the cells appear to be lodged on the intercalated duct. The relative surface area covered by MECs per terminal portion was also found to vary significantly, being 24% in the lactating mammary, 17% in the exorbital lacrimal, 48% in the sublingual, and 25% in the submandibular glands. The findings are discussed in relation to the physical properties of secretions in different glands.

In addition to their role in electrolyte homeostasis, striated ducts (SDs) in the major salivary glands of many mammalian species engage in secretion of organic products. This phenomenon usually is manifested as the presence of small serous-like secretory granules in the apical cytoplasm of SD cells. The composition of these granules is largely unknown, except in the case of the cat and rat submandibular gland, where the granules have unequivocally been shown to contain kallikrein. In some species, the apical cytoplasm of SD cells contains variable numbers of vesicles, both spherical and elongated, that vary in appearance from 'empty' to moderately dense. In the rat parotid gland, lucent vesicles transport glycoproteins to the luminal surface where they are incorporated into the apical plasmalemma and the glycocalyx. There is a strong possibility that in various species some of these vesicles are involved in transcytosis of antibodies to the saliva from their source (plasma cells) in the surrounding connective tissue. In addition, vesicles may engage in transfer of growth factors from the saliva to the interstitium. In a few species, conventional SDs have been replaced by ducts that are wholly given over to secretion, i.e., they entirely lack basal striations; although such ducts occupy the histological position of conventional SDs, it is not clear whether they represent a new type of duct or merely are modifications of SDs. Broad-based comparisons of ultrastructural and other data about SDs offer some insight into evolutionary history of salivary glands and their role in the adaptive radiation of mammals. Evolutionary patterns emerged when we made interspecific comparisons across mammalian orders. Among the bats, there is a clear relationship between SD secretion and general categories of diet. Anat Rec 264: 2001.

S U M M A R Y TNF-a alters leukocyte adhesion molecule expression of cultured endothelial cells like human umbilical vein endothelial cells (HUVEC). This study was designed to investigate the changes in vascular cell adhesion molecule-1 (VCAM-1), intercellular adhesion molecule-1 (ICAM-1), and platelet endothelial cell adhesion molecule-1 (PECAM-1) expression with TNF-a stimulation in cultured human neonatal dermal lymphatic endothelial cells (HNDLEC). The real-time quantitative PCR analysis on HNDLEC showed that TNF-a treatment leads to increases of VCAM-1 and ICAM-1 mRNAs to the 10.8-and 48.2-fold levels of untreated cells and leads to a reduction of PECAM-1 mRNA to the 0.42-fold level of untreated cells. Western blot and immunohistochemical analysis showed that TNF-a leads to VCAM-1 and ICAM-1 expressions that were inhibited by antiserum to human TNF receptor or by AP-1 inhibitor nobiletin. In flow cytometry analysis, the number of VCAM-1-and ICAM-1-positive cells increased, and PECAM-1-positive cells decreased with TNF-a treatment. Regarding protein amounts produced in cells and amounts expressed on the cell surface, VCAM-1 and ICAM-1 increased in HNDLEC and HUVEC, and PECAM-1 decreased in HNDLEC in a TNF-a concentration-dependent manner. VCAM-1, ICAM-1, and PECAM-1 protein amounts in TNFa-stimulated cells were lower in HNDLEC than in HUVEC. This suggests that the lymphatic endothelium has the TNF-a-induced signaling pathway, resulting in increased VCAM-1 and ICAM-1 expression to a weaker extent than blood endothelium and PECAM-1 reduction to a stronger extent than blood endothelium. (J Histochem Cytochem 55:721-733, 2007)

In an attempt to elucidate the effects of denervation on development and maintenance of the structure of the fungiform papilla, unilateral neurectomy of the chorda tympani-lingual nerve of rats was performed at day 1 and at weeks 1, 2, 3, 4, 7, and 10 after birth. Specimens were obtained at days 3, 7 and 10, weeks 2, 3, 4, 6, and 8, and months 3 and 4 after neurectomy for examination by light and scanning electron microscopy. At first, the fungiform papillae were atrophic, then progressed to forms resembling filiform papillae. When an immature fungiform papilla was denervated, it eventually changed to a papilla identical to normal filiform papillae. The elicited changes differed according to the time of neurectomy; it was found that early neurectomy resulted in a more rapid and marked morphological change of the fungiform papillae. The filiform-like papillae derived from the fungiform ones showed various shapes, sizes, and orientations and were rarely present on the unoperated control side of the lingual dorsum. Sections of the filiform-like papillae revealed that they had no taste buds. These findings suggest: (1) Morphogenesis and structural maintenance of the fungiform papillae require the presence of the chorda tympani and/or lingual nerve. (2) Completion of differentiation and maturation differ in time among fungiform papillae. (3) Fungiform papillae may be transformed filiform papillae induced and maintained by a neurotrophic factor or factors coming from the chorda tympani and/or lingual nerve. (4) Fungiform papillae are rarely innervated contralaterally.

The mucus elaborated by Weber's glands undoubtedly aids in swallowing dry food. We postulate that the serous cells in these glands, as in the more anterior von Ebner's glands, might play a role in the mechanism of taste, especially where posteriorly situated, nonlingual taste buds are concerned.