Regulation of angiotensin II production and angiotensin receptors in microvascular endothelial cells from bovine corpus luteum

被引:49
作者
Hayashi, K
Miyamoto, A
Berisha, B
Kosmann, MR
Okuda, K
Schams, D [1 ]
机构
[1] Tech Univ Munich, Inst Physiol, D-80350 Freising Weihenstephan, Germany
[2] Obihiro Univ Agr & Vet Med, Dept Anim Sci, Obihiro, Hokkaido 0808555, Japan
[3] Okayama Univ, Fac Agr, Lab Reprod Endocrinol, Okayama 7008530, Japan
关键词
D O I
10.1095/biolreprod62.1.162
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recent findings suggest that the ovarian renin-angiotensin system regulates ovarian function through the paracrine/autocrine actions of angiotensin (Ang) II. The aims of this study were to investigate 1) the endothelial cell capacity to convert Ang I to Ang II, 2) the effects of endocrine and paracrine/autocrine factors on Ang II production in microvascular endothelial cells (MVE) derived from the developing corpora lutea (CL), and 3) the relationship between Ang II peptide concentration and expression of mRNA for angiotensin type 1 and 2 receptors (ATR1 and AT2R) in the bovine Ct at different stages of the estrous cycle. When Ang I was added to the MVE at a concentration of 10(-9) M, it was converted to Ang II (21%). The production of Ang II from Ang I time-dependently rose for 24 h, Addition of captopril tan inhibitor of Ang-converting enzyme [ACE]) to the MVE cultures significantly inhibited Ang II production from 6 h to 24 h (P < 0.05). Addition of estradiol-17 beta (E-2) + vascular endothelial growth factor and E-2 + basic fibroblast growth factor to MVE cultures increased Ang II production, whereas E-2 or growth factors alone had no effect Specific transcription for AT1R and AT2R was detected in bovine CL and MVE. There were no significant changes in Ang II tissue concentration or AT1R mRNA expression using reverse transcription-polymerase chain reaction during the estrous cycle. In contrast, AT2R mRNA expression decreased during the midluteal phase (P < 0.05) and increased to the highest level during the late luteal phase (P < 0.05). Results demonstrated that Ang II is generated from Ang I in MVE isolated from the developing bovine Ct, indicating that MVE have ACE activity. In addition, mRNA expression for Ang II receptors was detected in the bovine Ct and the luteal MVE. These results suggest that Ang II is produced by actions of the local renin-angiotensin system, at least in part, on MVE in the bovine Ct, and that this peptide may be involved in the regulation of luteal function during early development and luteolysis.
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页码:162 / 167
页数:6
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