TY - JOUR
T1 - MicroRNA-126 suppresses the invasion of trophoblast-model JEG-3 cells by targeting LIN28A
AU - Pan, Xiaole
AU - Noguchi, Saki
AU - Ando, Misuzu
AU - Nishimura, Tomohiro
AU - Tomi, Masatoshi
N1 - Funding Information:
This study was supported by JSPS KAKENHI [grant numbers 18K14926 , 18H03183 , 20K21489 , 20K16056 ], Keio Gijuku Fukuzawa Memorial Fund for the Advancement of Education and Research , the Hoansha Foundation , and Keio University Doctoral Student Grant-in-Aid Program.
Publisher Copyright:
© 2021 Elsevier Inc.
PY - 2021/3/19
Y1 - 2021/3/19
N2 - Inadequate trophoblast invasion and impaired trophoblast-induced vascular remodeling are features of preeclampsia. In this context, an angiogenesis-related microRNA, miR-126, is abnormally expressed in preeclampsia placentas, but its role in trophoblast development remains unclear. The purpose of this study was to investigate the roles of miR-126 in the proliferation, migration, and invasion processes of trophoblast cells using the human choriocarcinoma-derived JEG-3 cell line as a model. The mRNA expression profiling of JEG-3 cells with and without miR-126 overexpression, in combination with bioinformatics analysis, identified LIN28A as a putative target of miR-126. The results of real-time RT-PCR and luciferase assay were consistent with this idea. Overexpression of miR-126 in JEG-3 cells decreased the invasive ability of the cells without affecting proliferation or migration. The invasiveness of JEG-3 cells was significantly reduced to a similar extent by knockdown of LIN28A with siRNA and by miR-126-overexpression-induced downregulation of LIN28A, although the level of LIN28A protein was much lower in the siLIN28A-transfected cells. These results indicate that miR-126 suppresses JEG-3 cell invasion by targeting LIN28A, and suggest that miR-126-mediated downregulation of LIN28A might contribute to the onset/deterioration of preeclampsia.
AB - Inadequate trophoblast invasion and impaired trophoblast-induced vascular remodeling are features of preeclampsia. In this context, an angiogenesis-related microRNA, miR-126, is abnormally expressed in preeclampsia placentas, but its role in trophoblast development remains unclear. The purpose of this study was to investigate the roles of miR-126 in the proliferation, migration, and invasion processes of trophoblast cells using the human choriocarcinoma-derived JEG-3 cell line as a model. The mRNA expression profiling of JEG-3 cells with and without miR-126 overexpression, in combination with bioinformatics analysis, identified LIN28A as a putative target of miR-126. The results of real-time RT-PCR and luciferase assay were consistent with this idea. Overexpression of miR-126 in JEG-3 cells decreased the invasive ability of the cells without affecting proliferation or migration. The invasiveness of JEG-3 cells was significantly reduced to a similar extent by knockdown of LIN28A with siRNA and by miR-126-overexpression-induced downregulation of LIN28A, although the level of LIN28A protein was much lower in the siLIN28A-transfected cells. These results indicate that miR-126 suppresses JEG-3 cell invasion by targeting LIN28A, and suggest that miR-126-mediated downregulation of LIN28A might contribute to the onset/deterioration of preeclampsia.
KW - Invasion
KW - LIN28A
KW - MicroRNA-126
KW - Placenta
KW - Trophoblast
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U2 - 10.1016/j.bbrc.2021.01.077
DO - 10.1016/j.bbrc.2021.01.077
M3 - Article
C2 - 33548626
AN - SCOPUS:85100398437
SN - 0006-291X
VL - 545
SP - 132
EP - 137
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
ER -