Expression of chemerin receptors CMKLR1, GPR1 and CCRL2 in the porcine pituitary during the oestrous cycle and early pregnancy and the effect of chemerin on MAPK/Erk1/2, Akt and AMPK signalling pathways

2020 ◽  
Vol 157 ◽  
pp. 181-198
Author(s):  
Katarzyna Kisielewska ◽  
Edyta Rytelewska ◽  
Marlena Gudelska ◽  
Marta Kiezun ◽  
Kamil Dobrzyn ◽  
...  
2022 ◽  
Vol 23 (2) ◽  
pp. 945
Author(s):  
Marlena Gudelska ◽  
Kamil Dobrzyn ◽  
Marta Kiezun ◽  
Katarzyna Kisielewska ◽  
Edyta Rytelewska ◽  
...  

Chemerin, belonging to the adipokine family, exhibits pleiotropic activity. We hypothesised that the adipokine could be involved in the regulation of steroidogenesis in the porcine endometrium. Thus, the aim of this study was to determine the effect of chemerin on the key steroidogenic enzyme proteins’ abundance (Western blot), as well as on P4 and E2 secretion (radioimmunoassay) by the porcine endometrium during early pregnancy and the mid-luteal phase of the oestrous cycle. Moreover, we investigated the hormone impact on Erk and Akt signalling pathway activation (Western blot). Chemerin stimulated E2 production on days 10 to 11 of pregnancy. On days 10 to 11 and 15 to 16 of gestation, and on days 10 to 11 of the cycle, chemerin enhanced the expression of StAR and all steroidogenic enzyme proteins. On days 12 to 13 of pregnancy, chemerin decreased StAR and most of the steroidogenic enzyme proteins’ abundance, whereas the P450C17 abundance was increased. On days 27 to 28 of pregnancy, chemerin increased StAR and P450C17 protein contents and decreased 3βHSD protein amounts. It was noted that the adipokine inhibited Erk1/2 and stimulated Akt phosphorylation. The obtained results indicate that chemerin affected P4 and E2 synthesis through the Erk1/2 and Akt signalling pathways.


PLoS ONE ◽  
2013 ◽  
Vol 8 (10) ◽  
pp. e75571 ◽  
Author(s):  
Lilian J. Oliveira ◽  
Nadéra Mansourri-Attia ◽  
Alan G. Fahey ◽  
John Browne ◽  
Niamh Forde ◽  
...  

1997 ◽  
Vol 12 (6) ◽  
pp. 1325-1337 ◽  
Author(s):  
A. Einspanier ◽  
M. R. Zarreh-Hoshyari-Khah ◽  
M. Balvers ◽  
L. Kerr ◽  
K. Fuhrmann ◽  
...  

Reproduction ◽  
2003 ◽  
pp. 621-627 ◽  
Author(s):  
RD Geisert ◽  
MD Ashworth ◽  

Attachment of the placenta to the uterus in pigs involves extracellular interaction between the expanding trophoblastic membrane and the thick glycocalyx present on the uterine epithelial microvilli. Formation of complexes between members of inter-alpha-trypsin inhibitor family may function in the maintenance of the extracellular matrix. This study investigated the change in the inter-alpha-trypsin inhibitor heavy chains (ITIH1, ITIH2, ITIH3 and ITIH4) during the oestrous cycle and early pregnancy in pigs. Gene expression of ITIH1, ITIH2, ITIH3 and ITIH4 was detected in the endometrium of cyclic and pregnant gilts; however, gene expression of ITIH was not altered throughout the oestrous cycle or early pregnancy. Western blot analysis with an ITIH antiserum identified the possible linkage forms of ITIH with the serine protease inhibitor, bikunin. Pregnancy altered the release of the various inter-alpha-inhibitor forms from the endometrium during the period of trophoblastic attachment. The results from this study indicate that the inter-alpha-trypsin inhibitor family plays an important role in maintenance of the uterine surface glycocalyx during placental attachment in pigs.


1995 ◽  
Vol 7 (5) ◽  
pp. 1053 ◽  
Author(s):  
TE Spencer ◽  
GH Graf ◽  
FW Bazer

This study determined effects of day of oestrous cycle and early pregnancy on sulfated glycoprotein-1 (SGP-1) expression in ovine endometrium. A 364-bp clone of the ovine SGP-1 mRNA was amplified from reverse transcribed Day-15 cyclic endometrial mRNA using the polymerase chain reaction (PCR) and primers specific for the rat SGP-1 mRNA sequence. Nucleotide sequence of the ovine SGP-1 cDNA shared significant identity with rat SGP-1 and human prosaposin. Ewes (n = 40) were hysterectomized on either Day 1, 6, 11, 13 or 15 of the oestrous cycle or on Day 11, 13, 15, 17 or 25 of early pregnancy. Total cellular RNA was isolated from endometrium and subjected to Northern and slot blot hybridization analyses using an antisense cRNA probe transcribed from the ovine SGP-1 cDNA clone. A single 2.6-kb mRNA transcript was detected by Northern hybridization analyses. Slot blot hybridization analyses indicated that steady-state levels of endometrial SGP-1 mRNA varied during the oestrous cycle (cubic, P < 0.02) and increased between Day 11 and Day 25 of early pregnancy (linear, P < 0.01). On Days 11, 13 and 15, endometrial SGP-1 mRNA levels were greater in pregnant ewes than in cyclic ewes (day x pregnancy status, P < 0.01). Immunohistochemical localization of SGP-1 in uterine tissues with rabbit anti-rat SGP-1 antibody revealed intense immunoreactivity associated primarily with the endometrial epithelium. These results indicate that the ovine endometrium expresses SGP-1, a prosaposin, and that SGP-1 expression varies during the oestrous cycle and is enhanced by the conceptus. The presence of SGP-1 in the endometrium suggests intracellular and extracellular roles for this protein in glycosphingolipid metabolism or transport in the uterine environment.


1977 ◽  
Vol 30 (4) ◽  
pp. 279 ◽  
Author(s):  
BG Miller ◽  
NW Moore ◽  
Leigh Murphy ◽  
GM Stone

The hormonal regulation of embryo development during early pregnancy in the ewe has been examined. Ovariectomized ewes received injections of oestradiol (E2) and progesterone (P) according to schedules designed to simulate endogenous ovarian secretion during the luteal phase of the previous oestrous cycle (priming P), around the time of oestrus (oestrous E2 ) and during early pregnancy (maintenance P, maintenance E2)' Embryos were transferred to the ewes on the 4th day after induced oestrus, and ewes were killed at 6 or 13 days after transfer to assess embryo development. Cytosol concentrations of oestradiol 'and progesterone receptors and RNA and protein metabolism in the endometrium and amounts of protein in uterine flushings were examined on the day of embryo transfer and 6 days after transfer.


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