Expression and localisation of epidermal growth factor receptors and their ligands in the lower genital tract of cycling cows

2019 ◽  
Vol 31 (11) ◽  
pp. 1692
Author(s):  
Hakan Saǧsöz ◽  
Narin Liman ◽  
Berna Güney Saruhan ◽  
Mehmet E. Akbalık ◽  
Muzaffer A. Ketani ◽  
...  

The 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.

2017 ◽  
Vol 28 (21) ◽  
pp. 2802-2818 ◽  
Author(s):  
Ralph Christian Delos Santos ◽  
Stephen Bautista ◽  
Stefanie Lucarelli ◽  
Leslie N. Bone ◽  
Roya M. Dayam ◽  
...  

Clathrin-mediated endocytosis is a major regulator of cell-surface protein internalization. Clathrin and other proteins assemble into small invaginating structures at the plasma membrane termed clathrin-coated pits (CCPs) that mediate vesicle formation. In addition, epidermal growth factor receptor (EGFR) signaling is regulated by its accumulation within CCPs. Given the diversity of proteins regulated by clathrin-mediated endocytosis, how this process may distinctly regulate specific receptors is a key question. We examined the selective regulation of clathrin-dependent EGFR signaling and endocytosis. We find that perturbations of phospholipase Cγ1 (PLCγ1), Ca2+, or protein kinase C (PKC) impair clathrin-mediated endocytosis of EGFR, the formation of CCPs harboring EGFR, and EGFR signaling. Each of these manipulations was without effect on the clathrin-mediated endocytosis of transferrin receptor (TfR). EGFR and TfR were recruited to largely distinct clathrin structures. In addition to control of initiation and assembly of CCPs, EGF stimulation also elicited a Ca2+- and PKC-dependent reduction in synaptojanin1 recruitment to clathrin structures, indicating broad control of CCP assembly by Ca2+ signals. Hence EGFR elicits PLCγ1-calcium signals to facilitate formation of a subset of CCPs, thus modulating its own signaling and endocytosis. This provides evidence for the versatility of CCPs to control diverse cellular processes.


2018 ◽  
Vol 130 ◽  
pp. 36-37
Author(s):  
Kaori Goto ◽  
Yasushi Kawano ◽  
Fumiko Kawabe ◽  
Yufuko Kai ◽  
Takafumi Utsunomiya ◽  
...  

2019 ◽  
Vol 112 (3) ◽  
pp. e254 ◽  
Author(s):  
Kaori Goto ◽  
Yasushi Kawano ◽  
Yufuko Kai ◽  
Yuichi Furukawa ◽  
Hiroko Itoh ◽  
...  

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