Prostaglandin (PTG) E and F receptors in the porcine corpus luteum; effect of tumor necrosis factor-α

被引:6
作者
Chang, J. [1 ]
Frandsen, S. [1 ]
D'Annibale-Tolhurst, M. [1 ]
Palumbo, N. [1 ]
Gadsby, J. [1 ]
机构
[1] North Carolina State Univ, Mol Biomed Sci, Coll Vet Med, 1060 William Moore Dr, Raleigh, NC 27606 USA
关键词
Pig; Corpus luteum; Prostaglandin receptors; TNF-alpha; Macrophages; Luteolytic sensitivity; ESTROUS-CYCLE; CORPORA-LUTEA; EARLY-PREGNANCY; MESSENGER-RNA; IMMUNE CELLS; EXPRESSION; LUTEOLYSIS; MACROPHAGES; PIG; BIOSYNTHESIS;
D O I
10.1016/j.anireprosci.2018.05.017
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
The porcine corpus luteum (CL) is NOT sensitive to the luteolytic effects of PGF-2 alpha until days 12-13 of cycle. The control of "luteolytic sensitivity" (LS) of the pig CL to PGF-2 alpha is unknown, but it is temporally associated with macrophage infiltration into the CL. Since macrophages are the predominant source of TNF-alpha in the porcine CL, in other studies we examined the effects of TNF-a on porcine luteal cells in culture and showed that TNF-a induces LS in vitro. In Experiment 1 of this study possible mechanisms involved in the control of LS were examined, and involved measurement of the protein levels of PTGER2/EP-2, and PTGER3/EP-3 in porcine CL collected before (days 7-10), versus after (day 13), the onset of the LS. In Experiment 2, an examination of potential mechanisms involved in the control of LS by TNF-alpha, was carried out in which the effects of TNF-a on mRNA and protein expression of EP-2, EP-3 and FP in cultured luteal cells, were examined. The results of Experiment 1 showed that PTGER-3/EP-3 (but not PTGER-2/EP-2) levels decreased in porcine CLs after (day 13) compared to before (day 7-10) LS. In Experiment 2, the data obtained showed that TNF-alpha decreased PTGER-3/EP-3 and increased PTGFR/FP protein (in EARLY stage CL). In conclusion, these studies suggest a role for PTGER-3/EP-3 in the acquisition of IS, and support the hypothesis that TNF-a from CL macrophages plays a critical role in the control of IS in the porcine CL, by increasing PTGFR/FP, and decreasing PTGER-3/EP-3 protein.
引用
收藏
页码:139 / 148
页数:10
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