Dopamine agonist inhibits vascular endothelial growth factor protein production and secretion in granulosa cells
© Ferrero et al. 2015
Received: 24 July 2015
Accepted: 3 September 2015
Published: 17 September 2015
Dopamine receptor 2 agonists (D2-ags) inhibit vascular endothelial growth factor (VEGF) secretion in luteinized granulosa cells (LGCs) both in vitro and in vivo. However, the mechanism of D2 regulation of the VEGF/VEGF Receptor 2 (VEGFR-2) pathway remains to be elucidated. We sought to determine the effects of D2 signaling on VEGF transcription and translation in LGCs, with the expectation of identifying potential D2-ag-based therapies for ovarian hyperstimulation syndrome (OHSS).
LGCs from egg donors were cultured with chorionic gonadotropin (hCG) in the presence of Actinomycin-D (ActD) or Brefeldin-A (BFA) to evaluate the effects of a D2-ag, cabergoline (Cb2), on VEGF secretion. The contribution of the conventional Gi/Go, Gz and AKT/β-Arrestin pathways in the VEGF regulation was assessed by adding pertussis toxin (PTX), phorbol 12-myristate 13-acetate (PMA), or wortmannin (WT). While Cb2 inhibited VEGF secretion by interfering with VEGF peptide translation and secretion, inhibition of conventional D2 transduction pathways did not reverse Cb2-mediated inhibition of VEGF secretion.
The effects of D2-ag on VEGF translation and secretion are mediated by D2 signaling pathways that have yet to be described. We found that D2-ag inhibits VEGF secretion at the post-transcriptional level, suggesting that D2-ag treatment should be combined with therapies that inhibit VEGF transcription, such as the employment of LH or GnRH for triggering ovulation, to improve the efficacy of OHSS prevention.
Ovarian hyperstimulation syndrome (OHSS) is an iatrogenic complication of ovarian stimulation associated with the use of human chorionic gonadotropin (hCG), is characterized by an increase in vascular permeability (VP) . Vascular endothelial growth factor (VEGF) is an important component in the development of OHSS [2, 3]. Besides, it has been demonstrated that hCG administration increases VEGF mRNA expression in luteinized granulosa cells (LCGs) [4, 5]. Several studies have attempted to avoid an increase in VEGF while employing GnRH agonists to induce ovulation [6, 7]; however, this strategy does not totally avoid OHSS onset , leaving a need for treatments that block VEGF/VEGF receptor 2 (VEGFR2) signaling completely.
Several in vivo [9, 10] and in vitro studies  have suggested a role for dopamine in the regulation of the VEGF/VEGFR2 pathway. Interestingly, high levels of dopamine are present in follicular fluid and human ovarian biopsies [12, 13], and dopamine receptors have been found on human granulosa cells (GCs) . Previous studies suggest a role for dopamine receptor agonist (D2-ag) in preventing VP increases [15, 16] by inhibiting VEGF secretion [17, 18]. However, D2-ag has previously been shown to block the onset of early-stage OHSS in 50 % of women at risk for developing the condition, but it was not effective in preventing the late onset form . Understanding the molecular mechanisms involved in D2 regulation of VEGF is critical to elucidating the role of D2-ag in OHSS prevention. Therefore, the goal of this study was to determine the molecular mechanism through which D2-ag inhibits VEGF secretion and to establish which D2 signaling pathways described in D2-expressing cells (Gi/Go, Gz and AKT/β-Arrestin)  are involved in the regulation of VEGF secretion.
LGCs were obtained from 24 egg donors [aged 25–30 years, oocytes retrieved = 10–15, estrogen (E2) < 2000 pg/mL, body mass index (BMI) < 30]. Cells were isolated by filtering , then washed and cultured as described below in the different studies. Written informed consent was provided by all participants, and the study protocol was approved by ethics committee of IVI Valencia.
VEGF mRNA is not altered by D2-agonist (Cabergoline)
D2-ag interferes with VEGF protein production and secretion
To determine whether Cb2 has translational or post-translational effects on VEGF production, LGCs (N = 6) were pre-incubated with a protein secretion inhibitor, Brefeldin-A (BFA; 10 μg/mL) (Sigma-Aldrich, St. Louis, US, A), for 1 h. Subsequently, LGCs were incubated in the presence or absence of Cb2 (100 μM) with 5 IU/mL hCG with or without 10 μg/mL BFA for 8 h. Extracellular and intracellular VEGF levels were measured using ELISA kits (R&D Systems, Minneapolis, US). Intracellular VEGF was confirmed by immunofluorescence using anti-VEGF antibody (10 μg/mL; R&D Systems Minneapolis, MN) and AlexaFluor594 antibody (1:500; R&D Systems Minneapolis, US). A fluorescence microscope was used to observe fluorescence (Nikon Eclipse E400, Japan), and images were acquired with a digital camera (Olympus, Tokyo, Japan). Signal intensity was assessed by Matlab (Worcester, MA), as previously described . The Student’s t-test was used for statistical analysis and a p-value less than 0.05 was considered statistically significant.
When protein secretion was inhibited by BFA, intracellular VEGF levels were lower in Cb2-treated than in untreated LGCs (Figs. 2b, c and 3a, b), suggesting that D2-ag also acts by inhibiting VEGF peptide production. Although there are studies suggesting that VEGF secretion can be regulated by the dopaminergic system [9, 10], none describe the mechanism how D2-agonists inhibit VEGF. In this regard, this is the first study showing that VEGF inhibition by D2-ag is specifically exerted at the post-transcriptional level with effect in of both peptide translation and subsequent releases once it has been produced, suggesting that D2-ag treatment should be combined with therapies to inhibit VEGF transcription, such as LH or GnRH agonists treatment for triggering ovulation, to improve the efficacy of OHSS prevention [6, 7].
The role of the conventional D2 transduction pathways in the modulation of VEGF secretion mediated by D2-ag
Based on our previous findings  it is unlikely that the D2 receptor is not involved in the process. Since the Gi/o, Gz, and AKT/β-arrestin signaling pathways are common intermediaries, it is possible that its inhibition might also be acting on pathways other than those transduced by D2, which might be involved in the VEGF regulation in LGCs. Therefore, it could explain why was not observe a counteracting increase in VEGF in response to treatment with PTX, PMA, or WT. The VEGF inhibition observed may be a result of D2-agonist-mediated transduction pathways that have yet to be described or alternative mechanisms that could be acting in well-known VEGF signaling pathways, such as FAK and MAPK pathways , PCL/PKC/Sp1 and adenylate cyclase/PKA/CREB pathways , or PI3k/AKT pathway . We are unaware whether VEGF regulation by D2-ag is a universal mechanism of angiogenesis control in many types of cells and conditions. If so, our findings, even if non-conclusive, could be useful at least to identify possible candidates involved in the process.
D2-agonists have also been considered for the treatment of tumorigenic conditions, such as ovarian cancer , in which the deregulation of the VEGF/VEGFR-2 pathways plays a major role. In this regard, investigation of the mechanism by which VEGF secretion is regulated by the dopaminergic system is needed to provide a basis for more specific therapies to treat diseases related to VEGF-mediated vascular angiogenesis, including OHSS.
Based on our findings, D2-ag in conjunction with clinical strategies aimed at reducing VEGF mRNA levels may provide a more powerful inhibitory effect on VEGF and improve efforts to prevent OHSS.
We thank Monterde Mercedes from Hospital La Fe for her assistance in the statistical analysis. We also give special thanks to all the medical and technical staff at the IVI clinic for their assistance in obtaining follicular fluid samples.
This work was supported by the Spanish Ministry of Economy and Competitiveness through the Miguel Servet Program [CP13/00077]; Carlos III Institute of Health grant [PI14/00547] awarded to R.G. and Spanish National and Valencian State Governments through SAF2008-03546 and Prometeo (20100613) grants awarded to A.P.
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