Key result
Forskolin-induced activation of the cAMP signaling pathway significantly enhanced the proliferation, invasion, and migration of HTR8/SV-neo trophoblast cells via the MAPK/ERK pathway.
Why the study?
Pre-eclampsia is thought to be related to placental dysfunction, particularly poor extravillous trophoblast invasion and migration, but the pathogenic mechanism is not fully understood.
Activation of the cAMP signaling pathway enhances trophoblast proliferation, invasion, and migration in vitro, providing a potential rationale for improving placental function in pre-eclampsia.
Answers are grounded in this paper and cite their sources.
May support cAMP pathway targeting in placental disorders; leaves open clinical translation from this in vitro model.
Pre-eclampsia (PE) is thought to be related to placental dysfunction, particularly poor extravillous trophoblast (EVT) invasion and migration abilities. However, the pathogenic mechanism is not yet fully understood. Here, we used the HTR8/SV-neo cell line as a model for the in vitro functional study of human extravillous trophoblasts. HTR8/SV-neo cells were treated with different concentrations of Forskolin solution (cAMP pathway-specific agonist) to alter intracellular cAMP level. Taking the DMSO group as the control group, firstly, cAMP assay kit was used to detect the cAMP concentration in HTR8/SV-neo cells treated with different concentration of Forskolin, and the cell proliferation function was detected by cell growth curve drawing and the colony formation experiment. The invasiveness and migration of cells were observed by Transwell experiments, and the expression of intracellular EMT-related markers was further evaluated by qPCR and WB experiments. According to our research, the intracellular cAMP level in HTR8/SV-neo cells was increased in a dose-dependently manner, and the proliferation, invasion and migration abilities of HTR8/SV-neo cells were significantly enhanced. Further detection by qPCR and WB experiments proved that the expression of EMT and angiogenesis markers in cells were up-regulated, including MMP2, PECAM, N-cadherin and VE-cadherin. In addition, with the increase of intracellular cAMP level, the phosphorylation level of intracellular MAPK signaling pathway was significantly increased. Thus, these results provide a novel rationale for the treatment of PE patients by improving the poor placental environment.
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Sun et al. (2023) studied Pre-eclampsia (in vitro model). Forskolin vs. DMSO control was evaluated on Cell proliferation, invasion, and migration. Forskolin-induced activation of the cAMP signaling pathway significantly enhanced the proliferation, invasion, and migration of HTR8/SV-neo trophoblast cells via the MAPK/ERK pathway.
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