Pregnancy-associated plasma protein-A (PAPP-A) in ovine, bovine, porcine, and equine ovarian follicles: Involvement in IGF binding protein-4 proteolytic degradation and mRNA expression during follicular development

被引:99
作者
Mazerbourg, S
Overgaard, MT
Oxvig, C
Christiansen, M
Conover, CA
Laurendeau, I
Vidaud, M
Tosser-Klopp, G
Zapf, J
Monget, P [1 ]
机构
[1] Univ Tours, INRA, CNRS, UMR 6073, F-37380 Nouzilly, France
[2] Aarhus Univ, Dept Mol & Struct Biol, DK-8000 Aarhus C, Denmark
[3] Statens Serum Inst, Dept Clin Biochem, DK-2300 Copenhagen S, Denmark
[4] Mayo Clin & Mayo Fdn, Endocrine Res Unit, Rochester, MN 55905 USA
[5] Fac Pharm, Genet Mol Lab, F-75006 Paris, France
[6] INRA, F-31326 Castanet Tolosan, France
[7] Univ Zurich Hosp, Dept Med, CH-8091 Zurich, Switzerland
关键词
D O I
10.1210/en.142.12.5243
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IGF binding protein-4 (IGFBP-4) proteolytic degradation is a common feature of preovulatory follicles from human, ovine, bovine, porcine, and equine ovary. In all these species, the protease is a zinc-dependent metalloprotease and its ability to degrade IGFBP-4 is IGF dependent. The human intrafollicular IGFBP-4-degrading protease has recently been identified as pregnancy-associated plasma protein-A (PAPP-A). The aim of this study was to investigate whether PAPP-A is also involved ed in IGFBP-4 degradation in ovine, bovine, porcine, and equine preovulatory follicles and to study the expression of PAPP-A mRNA in bovine and porcine granulosa cells from different classes of follicles. Immunoneutralization and immunoprecipitation with polyclonal antibodies raised against human PAPP-A inhibited IGFBP-4 proteolytic degradation in preovulatory follicular fluid from the four species studied. As previously reported for the intrafollicular proteolytic activity degrading IGFBP-4, recombinant human PAPP-A generated in vitro 17- and 10-kDa IGFBP-4-proteolytic fragments. Recombinant PAPP-A activity was also shown to be IGF dependent and was inhibited by heparin-binding domain-containing peptides. In all mammalian species studied, the PAPP-A sequences showed high degree of identity. Moreover, the PAPP-A gene was localized on porcine chromosome 1 (1q29-1q213), in agreement with the localization of human PAPP-A gene on human chromosome 9q33.1. In bovine and porcine ovaries, real-time quantitative RT-PCR showed that PAPP-A mRNA expression in granulosa cells was maximal in fully differentiated follicles and was positively correlated with expression of P450 aromatase and LH receptor mRNAs. Overall, these data show that PAPP-A is responsible for IGFBP-4 degradation in ovine, bovine, porcine, and equine preovulatory follicles. The high expression of PAPP-A mRNA in granulosa cells from large, differentiated follicles suggest that it is a new functional marker of follicular development.
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页码:5243 / 5253
页数:11
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