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Inhibitory effect of all-trans retinoic acid on ferroptosis in BeWo cells mediated by the upregulation of heme Oxygenase-1.

Authors :
Matsuoka, Tomona
Kajiwara, Kazuhiro
Kawasaki, Tomoyuki
Wada, Seiji
Samura, Osamu
Sago, Haruhiko
Okamoto, Aikou
Umezawa, Akihiro
Akutsu, Hidenori
Source :
Placenta; Sep2024, Vol. 154, p110-121, 12p
Publication Year :
2024

Abstract

This study aimed to explore the association between ferroptosis, a newly identified type of cell death, and the role of retinoic acid in developing pregnancy complications. Therefore, the effects of all-trans retinoic acid (ATRA) on ferroptosis susceptibility in BeWo cells were assessed to understand abnormal placental development. BeWo cells were used as surrogates for cytotrophoblasts. The effect of ATRA on ferroptosis sensitivity was assessed on BeWo cells pretreated with ATRA or dimethyl sulfoxide (DMSO; control), following which the LDH-releasing assay was performed. The effects of ATRA pretreatment on the antioxidant defense system (including glutathione [GSH], mitochondrial membrane potential, and heme oxygenase-1 [HMOX1]) in BeWo cells were assessed using assay kits, RT-qPCR, and HMOX1 immunostaining. To evaluate the effect of ATRA on BeWo cells, HMOX1 was silenced in BeWo cells using shRNA. ATRA pretreatment increased ferroptosis resistance in BeWo cells. Although with pretreatment, qPCR indicated upregulation of HMOX1, no significant change was observed in the GSH levels or mitochondrial membrane potential. This was corroborated by intensified immunostaining for heme oxygenase-1 protein (HO-1). Notably, the protective effect of ATRA against ferroptosis was negated when HO-1 was inhibited. Although HMOX1-silenced BeWo cells exhibited heightened ferroptosis sensitivity compared with controls, ATRA pretreatment counteracted ferroptosis in these cells. ATRA pretreatment promotes BeWo cell viability by suppressing ferroptosis and upregulating HMOX1 and this can be used as a potential therapeutic strategy for addressing placental complications associated with ferroptosis. [Display omitted] • ATRA pretreatment in BeWo cells suppresses ferroptosis. • The inhibitory effect of ATRA on ferroptosis is mediated by retinoic acid receptor β. • ATRA pretreatment in BeWo cells upregulates HMOX1. • HMOX1 knockdown cells have increased susceptibility to ferroptosis. • ATRA pretreatment in HMOX1 knockdown cells decreased susceptibility to ferroptosis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01434004
Volume :
154
Database :
Supplemental Index
Journal :
Placenta
Publication Type :
Academic Journal
Accession number :
179368742
Full Text :
https://doi.org/10.1016/j.placenta.2024.06.012