Autophagy-Related Proteins, LC3 and Beclin-1, in Placentas From Pregnancies Complicated by PreeclampsiaDepartment of Obstetrics and Gynecology, Sungkyunkwan University School of Medicine, Seoul, South Korea, crroh{at}skku.edu
Department of Obstetrics and Gynecology, Sungkyunkwan University School of Medicine, Seoul, South Korea
Department of Obstetrics and Gynecology, Sungkyunkwan University School of Medicine, Seoul, South Korea
Department of Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea
Department of Obstetrics and Gynecology, Sungkyunkwan University School of Medicine, Seoul, South Korea
Department of Obstetrics and Gynecology, Sungkyunkwan University School of Medicine, Seoul, South Korea
The objective of this study is to investigate the expression of autophagy-related proteins (LC3 and beclin-1) in human placentas and the changes they undergo in the placentas from pregnancies complicated by preeclampsia (PE) and to explore the regulatory mechanisms of these proteins in JEG-3 cells in response to hypoxia or cytokine treatment.The presence of autophagosomes was confirmed with electron microscopy and the expression of LC3 and beclin-1 by immunoimaging methods in human placental trophoblasts. Compared with the placentas from normal pregnancies, the expression of LC3-II protein, but not beclin-1, was increased in the placentas from severe PE. In JEG-3 cells, hypoxia (O2 < 1%) induced a modest but not significant increase in the expression of LC3-II with a significant decrease in the expression of beclin-1. Meanwhile, TNF-
Key Words: Placenta autophagy preeclampsia beclin-1 LC3.
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treatment induced a significant increase in the expression of LC3-II without a significant change in the expression of beclin-1. Our data suggests that increased autophagic activity in the placenta may be implicated in the pathophysiology of PE. 