Edward B. Messelt

Localization of AQP5 during development of the mouse submandibular salivary gland

Aquaporin 5 (AQP5) is known to be central for salivary fluid secretion. A study of the temporal-spatial distribution of AQP5 during submandibular gland (SMG) development and in adult tissues might offer further clues to its unknown role during development. In the present work, SMGs from embryonic day (E) 14.5–18.5 and postnatal days (P) 0, 2, 5, 25, and 60 were immunostained for AQP5 and analyzed using light microscopy. Additional confocal and transmission electron microscopy were performed on P60 glands. Our results show that AQP5 expression first occurs in a scattered pattern in the late canalicular stage and becomes more prominent and organized in the terminal tubuli/pro-acinar cells towards birth. Additional apical membrane staining in the entire intralobular duct is found just prior to birth. During postnatal development, AQP5 is expressed in both the luminal and lateral membrane of pro-acinar/acinar cells. AQP5 is also detected in the basal membrane of acinar cells at P25 and P60. In the intercalated ducts at P60, the male glands show apical staining in the entire segment, while only the proximal region is positive in the female glands. These results demonstrate an evolving distribution of AQP5 during pre- and postnatal development in the mouse SMGs.

Selective brain cooling and its vascular basis in diving seals.

SUMMARY Brain (Tbrain), intra-aorta (Taorta), latissimus dorsi muscle (Tm) and rectal temperature (Tr) were measured in harp (Pagophilus groenlandicus) and hooded (Cystophora cristata) seals during experimental dives in 4°C water. The median brain cooling was about 1°C during 15 min diving, but in some cases it was as much as 2.5°C. Cooling rates were slow for the first couple of minutes, but increased significantly after about 5 min of diving. The onset of cooling sometimes occurred before the start of the dive, confirming that the cooling is under cortical control, like the rest of the diving responses. Taorta also fell significantly, and was always lower than Tbrain, while Tm was fairly stable during dives. Detailed studies of the vascular anatomy of front flippers revealed that brachial arterial blood can be routed either through flipper skin capillaries for nutritive purposes and return through sophisticated vascular heat exchangers to avoid heat loss to the environment, or, alternatively, through numerous arterio-venous shunts in the skin and return by way of large superficial veins, which then carry cold blood to the heart. In the latter situation the extent to which the brain is cooled is determined by the ratio of carotid to brachial arterial blood flow, and water temperature, and the cooling is selective in that only those organs that are circulated will be cooled. It is concluded that Tbrain is actively down-regulated during diving, sometimes by as much as 2.5°C, whereby cerebral oxygen requirements may be reduced by as much as 25% during extended dives.

Gut length, food transit time and diving habit in phocid seals

Abstract The southern elephant seal (Mirounga leonina) has the ability to dive for 2 h and reach depths of 1200 m. This creature is also exceptional in having a small intestine that is 25 times body length. Krockenberger and Bryden advanced the hypothesis that the long small intestine has developed to compensate for the extended periods with reduced or even abolished intestinal blood perfusion during diving. To test this hypothesis we have measured small-intestinal lengths in crabeater (Lobodon carcinophagus), Weddell (Leptonychotes weddellii), Ross (Ommatophoca rossi), leopard (Hydrurga leptonyx), harp (Phoca groenlandica), ringed (Phoca hispida) and hooded (Cystophora cristata) seals and related them to available data on their maximal dive duration. We found no significant correlation (P > 0.05) between intestinal length relative to body length and diving ability, but we found that small-intestinal internal area was significantly (P < 0.05) related to body length. A crude scanning electron microscopical examination of the small intestines of Weddell, crabeater, hooded and harp seals failed to reveal any gross anatomical differences between small-intestinal surfaces. This suggests that gut dimension in this variety of phocid species with widely differing diving ability is not related to diving habit, but is instead related to body size. The transit time of digesta was determined in two 1-year-old harp seals by use of radiopaque polyethylene rings of 4-mm diameter followed by X-ray examination, as markers for the solid phase passage, and chromium ethylene-diaminetetra acetic acid (Cr-EDTA) as a marker for the liquid phase. The transit time for the Cr-EDTA marker was 6.9 h ± 0.5 SE (range 4.5–8 h, n= 7), while 80% of the polyethylene markers appeared in the colon after 17.6 h ± 1.0 SE (range 14–21.5 h, n= 6) and were sometimes retained in the colon for several hours before defecation. These transit times did not change significantly (P > 0.05) in response to repetitive diving over a period of 8 h. This indicates that the often-used Cr-EDTA is not a good measure for digesta passage time when used alone in seals, and that the hypothesis of Krockenberger and Bryden is most likely wrong.

Comparison of the Histology, Gene Expression Profile, and Phenotype of Cultured Human Limbal Epithelial Cells from Different Limbal Regions

PURPOSE To investigate whether human limbal epithelial cells (HLECs) derived from various regions of the limbus exhibit differences in gene expression and epithelial characteristics. METHODS HLECs were derived from explants taken from the superior, nasal, inferior, and temporal limbus and cultured for 21 days. Whole genome transcript profiling was performed with a gene microarray. The microarray results were validated by using RT-PCR. Epithelial morphology was studied with light microscopy and transmission electron microscopy, and phenotype was evaluated by immunohistochemistry. RESULTS Epithelial outgrowth was present in most cultures of superior origin (88%) in contrast to cultures of temporal origin (38%). The epithelial thickness and number of cell layers were significantly greater in cultures of superior origin than in cultures from inferior and temporal areas. TRIM36, OSR2, and RHOU, which are involved in morphogenesis, were significantly differentially expressed in the superior region, compared with the other regions. Proposed limbal stem cell, progenitor, and differentiation markers were not differentially expressed. The uniform gene expression of ocular surface markers correlated with homogeneous immunostaining of corresponding protein markers in HLEC cultures from all regions, demonstrating an undifferentiated phenotype (p63(+), DeltaNp63alpha(+), ABCG2(+), K19(+), vimentin(+), integrin beta1(+), nestin(-), K3(-), K5(+), and E-cadherin(+)). CONCLUSIONS No major transcriptional or phenotypic differences were observed in cultured HLECs derived from different regions of the limbus. However, explants of superior origin demonstrated the highest outgrowth success rate and generated epithelia with greater epithelial thickness and number of cell layers, which may prove useful for transplantation purposes.

Trefoil factor family 3 expression in the oral cavity.

This study examined the expression, in oral keratinocytes and in the major and minor salivary glands, of Trefoil factor family 3 (TFF3) peptide. Trefoil factor family 3 messenger RNA (mRNA) and peptide were detected in cultures of normal oral keratinocytes by quantitative real-time polymerase chain reaction (PCR) and western blotting, respectively. Trefoil factor family 3 was found, by immunohistochemical analyses, to be expressed in the basal layers of the oral mucosal epithelium. In salivary glands, immunohistochemical staining showed that TFF3 peptide expression was strongest in the mucous acini of the submandibular and the small salivary glands. Serous cells in the same glands showed weak staining. In the parotid gland, many serous acini showed weak positive staining, while other areas did not. In all glands examined, the intercalated, striated, and collecting ducts were moderately TFF3-positive. Double immunostaining confirmed that mucous (MUC5B positive) cells were moderately or strongly positive for TFF3 and that some serous (MUC7 positive) cells showed restricted TFF3 expression, mostly in a granular pattern. The prevalence of the TFF3 peptide in the salivary secretions of healthy volunteers was detected by western blotting of saliva from minor salivary glands (four of five) and the parotid gland (one of five) and of mixed submandibular/sublingual saliva (five of five). In conclusion, the submandibular and small salivary glands appear to be the major producers of oral TFF3, but duct cells of all glands and keratinocytes of the oral mucosa may also contribute as sources of TFF3 in the oral cavity.

Optimization of Storage Temperature for Cultured ARPE-19 Cells

Purpose. The establishment of future retinal pigment epithelium (RPE) replacement therapy is partly dependent on the availability of tissue-engineered RPE cells, which may be enhanced by the development of suitable storage methods for RPE. This study investigates the effect of different storage temperatures on the viability, morphology, and phenotype of cultured RPE. Methods. ARPE-19 cells were cultured under standard conditions and stored in HEPES-buffered MEM at nine temperatures (4°C, 8°C, 12°C, 16°C, 20°C, 24°C, 28°C, 32°C, and 37°C) for seven days. Viability and phenotype were assessed by a microplate fluorometer and epifluorescence microscopy, while morphology was analyzed by scanning electron microscopy. Results. The percentage of viable cells preserved after storage was highest in the 16°C group (48.7% ± 9.8%; P < 0.01 compared to 4°C, 8°C, and 24°C–37°C; P < 0.05 compared to 12°C). Ultrastructure was best preserved at 12°C, 16°C, and 20°C. Expression of actin, ZO-1, PCNA, caspase-3, and RPE65 was maintained after storage at 16°C compared to control cells that were not stored. Conclusion. Out of nine temperatures tested between 4°C and 37°C, storage at 12°C, 16°C, and 20°C was optimal for maintenance of RPE cell viability, morphology, and phenotype. The preservation of RPE cells is critically dependent on storage temperature.

Influence of X-ray irradiation on the ultrastructure of rat submandibular gland striated-duct cells

Previous investigations have indicated that striated-duct cells react to stimulation with an apocrine secretion, morphologically demonstrated by bleb-like projections of the apical cytoplasm. Since bleb formation as an ultrastructural feature also has been debated and sometimes interpreted as a fixation artifact, it was considered essential to extend the studies by exposing the submandibular gland to X rays to establish whether such treatment would have any influence on the formation of blebs. The material used in the present study consisted of rat submandibular glands exposed to X rays in the range of 200-1800 rad. The glands were examined by both SEM and TEM. The duct cells exposed to 200 rad appeared normal, with no sign of alteration in their ability to produce blebs, whereas duct cells exposed to 750 rad showed no sign of bleb formation. Some of the duct cells exposed to 1800 rad showed considerable morphological changes, consistent with oncotic transformation. The results support the conclusion that bleb formation is a normal morphological feature and not an artifact. This study also indicates that the functional activity of the cells is reduced after exposure to X rays.

Ultrastructural studies on the bleb formation in seal and rat submandibular gland striated ducts.

For the present study Seal (Phoca vitulina) and rat submandibular gland striated ducts were investigated by electron microscopy. Both normal and stimulated animals (starved for 24 h and then fed 2 h before the tissues were removed) were examined. Basal invaginations of the cell membrane with areas heavily loaded with mitochondria were typical features of both animals. Secretory granules were especially numerous in the apical part of stimulated duct cells. The granules were separated from the luminal membrane of the cells by a condensed area called the spearating zone. Apical protrusions or blebs, which were frequently occurring in striated ducts of both animals, are interpreted as manifestations of apocrine secretion. It was concluded that this way of apocrine secretion is a fundamental function, since seals, which have salivary glands of a rather simple composition with acini which are functionally reduced, have retained the ability to form blebs.

Distribution of nerve growth factor, pro‐nerve growth factor, and their receptors in human salivary glands

Nerve growth factor (NGF) is a pluripotent mediator that is present in a range of human tissues. Nerve growth factor was originally considered important only in neuronal homeostasis and pathophysiology, but later it was also implicated in the pathophysiology of inflammation, epithelial differentiation, and wound healing. In this study, the distribution of nerve growth factor beta (NGF-β) and pro-NGF, and their receptors - tyrosine kinase A (TrkA) and p75(NTR) - was examined in human parotid, submandibular, sublingual, and labial salivary glands by immunohistochemistry. Intercalated, striated, and collecting-ducts in all gland types showed strong staining for pro-NGF but only weak cytoplasmic or sparse nuclear staining for NGF-β. Tyrosine kinase A was strongly expressed in the ducts of all gland types, whereas p75(NTR) expression was mainly confined to collecting ducts. In acini, no or only weak cytoplasmic staining was found for all markers, and some nuclei stained positive for NGF-β, pro-NGF, and TrkA. Western blotting of saliva showed secretion of several forms of pro-NGF, while no mature NGF-β was detected. Salivary pro-NGF may play a role in oral wound healing.

The impact of de-epithelialization of the amniotic membrane matrix on morphology of cultured human limbal epithelial cells subject to eye bank storage.

Purpose: To investigate whether human limbal epithelial cells (HLEC) that have been cultured on intact or de-epithelialized amniotic membranes (AMs) demonstrate differences in morphology after 1 week of eye bank storage. Methods: HLEC were cultured from limbal explants for 3 weeks on intact AM and AM deprived of the amniotic epithelial cells by incubation with 0.02% ethylene diamine tetra acetic acid followed by mechanical scraping. The HLEC cultures were stored for 1 week in a closed container in a serum-based medium at 23°C. The surface morphology was assessed using scanning electron microscopy, and a quantitative comparison of desmosome and hemidesmosome numbers was performed using transmission electron microscopy. Results: Although most superficial epithelial cells were closely attached to each other, with tightly opposed cell junctions and distinct cell borders, there was evidence of some cell separation in HLEC that had been cultured on intact and denuded AM after 1 week of storage. In both experimental groups, the epithelia were well stratified, consisting of basal column-shaped cells, suprabasal cuboid wing cells, and flat squamous superficial cells, but dilated intercellular spaces were observed. The total number of desmosomes per micron was 1.39 ± 0.77 in HLEC cultured on intact AM versus 0.98 ± 0.45 in HLEC expanded on denuded AM (P = 0.76). The total number of hemidesmosomes per micron in HLEC cultured on intact AM and denuded AM was 0.87 ± 0.34 and 0.78 ± 0.31, respectively (P = 0.70). Conclusions: Denuding of AM does not improve the structural integrity of cultured HLEC after eye bank storage.