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Updated: Dec 22, 2025

A Modified Co-Culture System for Understanding Granulosa-Theca Cell Interactions in the Bovine Ovary
Published on: September 19, 2025
Transforming growth factor-beta family members are regulated during induced luteolysis in cattle
Cristina Sangoi Haas1, Monique Tomazele Rovani1, Gustavo Freitas Ilha2
1Universidade Federal de Pelotas, Departamento de Patologia Animal, Capão do Leão, RS, Brasil.
Abstract:
The transforming growth factors beta (TGFβ) are local factors produced by ovarian cells which, after binding to their receptors, regulate follicular deviation and ovulation. However, their regulation and function during corpus luteum (CL) regression has been poorly investigated. The present study evaluated the mRNA regulation of some TGFβ family ligands and their receptors in the bovine CL during induced luteolysis in vivo. On day 10 of the estrous cycle, cows received an injection of prostaglandin F2α (PGF) and luteal samples were obtained from separate groups of cows (n= 4-5 cows per time-point) at 0, 2, 12, 24 or 48 h after treatment. Since TGF beta family comprises more than 30 ligands, we focused in some candidates genes such as activin receptors (ACVR-1A, -1B, -2A, -2B) AMH, AMHR2, BMPs (BMP-1, -2, -3, -4, -6 and -7), BMP receptors (BMPR-1A, -1B and -2), inhibin subunits (INH-A, -BA, -BB) and betaglycan (TGFBR3). The mRNA levels of BMP4, BMP6 and INHBA were higher at 2 h after PGF administration (P<0.05) in comparison to 0 h. The relative mRNA abundance of BMP1, BMP2, BMP3, BMP4, BMP6, ACVR1B, INHBA and INHBB was upregulated up to 12 h post PGF (P<0.05). On the other hand, TGFBR3 mRNA that codes for a reservoir of ligands that bind to TGF-beta receptors, was lower at 48 h. In conclusion, findings from this study demonstrated that genes encoding several TGFβ family members are expressed in a time-specific manner after PGF administration.
Insights
Transforming growth factors beta (TGFβ) gene expression in bovine corpus luteum (CL) was investigated during induced luteolysis. Key TGFβ family members showed time-specific mRNA regulation following prostaglandin F2α (PGF) administration, revealing their roles in CL regression.
Area of Science:
- Reproductive biology
- Endocrinology
- Molecular biology
Background:
- Transforming growth factors beta (TGFβ) are crucial local ovarian factors regulating follicular development and ovulation.
- The specific roles and regulation of TGFβ signaling during corpus luteum (CL) regression remain largely uncharacterized.
Purpose of the Study:
- To investigate the mRNA regulation of selected TGFβ family ligands and their receptors in the bovine CL during prostaglandin F2α (PGF)-induced luteolysis.
- To understand the temporal expression patterns of TGFβ signaling components during CL regression.
Main Methods:
- Bovine corpus luteum (CL) samples were collected at various time points (0, 2, 12, 24, 48 hours) after PGF administration on day 10 of the estrous cycle.
- Quantitative real-time PCR was used to measure the mRNA levels of specific TGFβ family genes, including activin receptors, AMH, BMPs, BMP receptors, inhibin subunits, and betaglycan.
Main Results:
- mRNA levels of BMP4, BMP6, and INHBA were significantly elevated at 2 hours post-PGF treatment.
- Upregulation of BMP1, BMP2, BMP3, BMP4, BMP6, ACVR1B, INHBA, and INHBB mRNA was observed up to 12 hours after PGF administration.
- A significant decrease in TGFBR3 mRNA abundance was noted at 48 hours post-PGF treatment.
Conclusions:
- The study demonstrates that genes encoding various TGFβ family members are expressed in a time-specific manner in the bovine CL following PGF-induced luteolysis.
- These findings highlight the dynamic involvement of TGFβ signaling in the complex process of CL regression.
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