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Öğe Expression and localisation of epidermal growth factor receptors and their ligands in the lower genital tract of cycling cows(Csiro Publishing, 2019) Sagsoz, Hakan; Liman, Narin; Saruhan, Berna Guney; Akbalik, Mehmet E.; Ketani, Muzaffer A.; Topaloglu, UgurThe epidermal growth factor receptor (ErbB) family and its ligands are essential for the regulation of multiple cellular processes required for mammalian reproduction. The objectives of this study were to investigate the expression and localisation of ErbB subtypes (ErbB1-4) and selected ligands, namely epidermal growth factor (EGF), amphiregulin (AREG) and neuregulin (NRG), in the cervix and vagina of cycling cows and to determine possible steroid hormone-dependence of their expression using immunohistochemistry. All four ErbBs and EGF, AREG and NRG proteins were found to be localised in the nucleus and cytoplasm of different cells in the cervix and vagina, and their expression differed during the oestrous cycle. During the follicular phase, in both the cervix and vagina, ErbB1, ErbB2, ErbB3, ErbB4 and EGF expression was higher in the luminal epithelium (LE) than in stromal and smooth muscle (SM) cells (P<0.05). During the luteal phase, the expression of ErbB1, ErbB3 and EGF in the LE was significantly different from that in stromal and SM cells in the cervix, whereas the expression of EGF and AREG differed in the vagina compared to the cervix (P<0.05). Throughout the oestrous cycle, in both the cervix and vagina, although ErbB2/human epidermal growth factor receptor 2 expression in the LE and SM cells was significantly higher than in the stromal cells (P<0.05), NRG expression was similar in the LE, stromal and SM cells (P>0.05). Overall, these results suggest that all four ErbBs and the EGF, AREG and NRG proteins may collectively contribute to several cellular processes in the bovine cervix and vagina during the oestrous cycle.Öğe Functional characteristics of the growth factor receptor family and some ligands in the oropharyngeal cavity of the Chukar partridge (Alectoris chukar)(Taylor & Francis Ltd, 2015) Saruhan, Berna G.; Sagsoz, Hakan; Akbalik, Mehmet E.; Erdogan, Serkan1. The aim of the present study is to describe, immunohistochemically, the expression and cell type localisation of growth factor receptors and some of their ligands in the oropharyngeal organs of the Chukar partridge. 2. The tissue samples from 10 healthy adult partridges were dissected under ether anaesthesia and then embedded in paraffin following routine histological procedures. The immunoreaction for receptors and ligands of the epidermal growth factor receptor (EGFR)/ligand system was localised in the cell membrane, nucleus and cytoplasm of the luminal and glandular epithelial cells, stromal and striated muscle cells, and vascular endothelial and smooth muscle cells. 3. Variations were observed in the avian oropharyngeal organs. The immunostaining for the erbB1/HER1 (human epidermal growth factor receptor 1) and the EGF (epidermal growth factor) and AREG (Amphiregulin) ligands in the luminal epithelial cells was higher than in the glandular epithelial, stromal and striated muscle cells. However, the immunostaining for erbB3/HER3 (human epidermal growth factor receptor 3) and erbB4/HER4 (human epidermal growth factor receptor 4) were similar in the luminal epithelium, stromal and striated muscle cells. 4. Growth factor receptors and some of their ligands were localised in different cell types in the oropharyngeal organs. We suggest that erbB/HERs (human epidermal growth factor receptors) and their ligands play an important role in proliferation, differentiation, growth, survival and migration of the cells.Öğe Histomorphological structure of the palate and histochemical profiles of the salivary palatine glands in the Chukar partridge (Alectoris chukar, Gray 1830)(Wiley-Blackwell, 2013) Sagsoz, Hakan; Erdogan, Serkan; Akbalik, Mehmet E.Morphology of the palatine mucosa and its secretion was described in Chukar partridges, by gross morphology and histochemistry techniques. For this purpose, 10 healthy adults (five male and five female) were sacrificed. After sacrifice, the palatine tissues were extirpated and fixed in 10% formol-alcohol for 18h and were embedded longitudinally and transversally in paraffin. The 5-m sections were employed histological and histochemical staining techniques. The lateral rims of the caudal part of the choanal cleft were bordered by large conical papillae. In the periphery of the choanal and the infundibular cleft, small papillae were scattered across the palatine mucosa. The palate was lined by keratinized stratified squamous epithelium, which contained conical papillae of varying height. However, the folds of the keratinized stratified squamous epithelial layer covering the choanal and infundibular cleft were nonkeratinized. The rostral aspect of the choanal cleft contained simple branched tubulo-alveolar glands of both mucous and sero-mucous characteristic, whilst the caudal aspect included mucous simple branched tubular glands. Furthermore, it was ascertained that the secretion of the palatine glands contained glycoproteins, carboxylated proteoglycans, weakly and strongly sulphated mucins, sialic acid and hyaluronic acid, but lacked glycogen. In conclusion, it was demonstrated that the histological structure of the mucosal epithelium and the supporting elements displayed similarity to those of other domestic avian species.Öğe Osteopontin expression in the intestine of chukar partridge (Alectoris chukar, Gray, 1830)(Brill Academic Publishers, 2015) Akbalik, Mehmet E.; Sagsoz, Hakan; Erdogan, SerkanThe intestinal mucosa is under continuous attack of microorganisms and is defended by the joint action of epithelial cells and specialized immune cells. Osteopontin (OPN), a member of the Small Integrin-Binding Ligand, N-linked Glycoprotein (SIBLING) family, is an adhesive phosphorylated glyco-protein that is synthesized by a variety of nonimmune and immune cells that is involved in interactions with cells mediating signaling. OPN is especially required for the maintenance of the epithelial barrier. To gain a better understanding of the biology of OPN, in the avian intestinal tract, we examined subcellular localization of OPN in the small and large intestine using immunohistochemistry. Immunostaining for OPN was prominently and significantly detected in the epithelial cells of the small and large intestine. However, intestinal stromal cells of the small intestine and the smooth muscle cells in the wall of the large intestine did not exhibit OPN immunoreactivity. Our results show that the differences between the localizations of OPN in the chukar partridge's small and large intestine may be associated with functional differences of intestine parts. Therefore, the expression of OPN in the chukar partridge intestine may play a crucial role in barrier function, host defence, and/or secretion.