Expressions of lipoprotein receptors and cholesterol efflux regulatory proteins during luteolysis in bovine corpus luteum
Author(s) -
Kei Horihata,
Shin Yoshioka,
Masahiro Sano,
Yuki Yamamoto,
Koji Kimura,
Dariusz J. Skarżyński,
Kiyoshi Okuda
Publication year - 2016
Publication title -
reproduction fertility and development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.609
H-Index - 76
eISSN - 1448-5990
pISSN - 1031-3613
DOI - 10.1071/rd15538
Subject(s) - corpus luteum , luteolysis , luteal phase , abca1 , medicine , endocrinology , ldl receptor , receptor , scavenger receptor , abcg1 , steroidogenic acute regulatory protein , biology , lipoprotein , cholesterol , chemistry , messenger rna , biochemistry , ovary , transporter , hormone , gene
The corpus luteum (CL) synthesises and secretes progesterone (P4), which is essential for the establishment and maintenance of pregnancy in mammals. P4 is synthesised from cholesterol. Cholesterol is internalised by low-density lipoprotein receptor (LDLR) and/or scavenger receptor B1 (SR-BI), and is effluxed by ATP-binding cassette (ABC) transporter A1 (ABCA1) and G1 (ABCG1). To test the hypothesis that lipoprotein receptors and ABC transporters are involved in functional luteolysis, we examined the expression of LDLR, SR-BI, ABCA1 and ABCG1 in bovine CL during the luteal stages and after injection of prostaglandin (PG) F 2α on Day 10 after ovulation. Expression of LDLR and SR-BI mRNA and protein was lower in the regressed luteal than late luteal stage. Injection of cows with a PGF 2α did not affect LDLR mRNA and protein levels in the CL. Although expression of SR-BI mRNA did not change, SR-BI protein expression decreased 12 and 24h after PGF 2α injection. The overall findings of the present study suggest that the decreased expression of SR-BI induced by PGF 2α is one of the factors responsible for the continuous decrease in P4 production during functional luteolysis.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom