4.5 Article

The Unique Expression and Function of miR-424 in Human Placental Trophoblasts

Journal

BIOLOGY OF REPRODUCTION
Volume 89, Issue 2, Pages -

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1095/biolreprod.113.110049

Keywords

FGFR1; hypoxia; microRNA; miR-424; trophoblasts

Funding

  1. State of Pennsylvania Department of Health Formula Research Funds
  2. Magee Womens Research Institute
  3. National Institutes of Health [R01HD065893, R21HD071707]

Ask authors/readers for more resources

Placental hypoperfusion causes cellular hypoxia and is associated with fetal growth restriction and preeclampsia. In response to hypoxia, the repertoire of genes expressed in placental trophoblasts changes, which influences key cellular processes such as differentiation and fusion. Diverse miRNAs were recently found to modulate the cellular response to hypoxia. Here we show that miR-424, which was previously shown to be upregulated by hypoxia in nontrophoblastic cell types, is uniquely downregulated in primary human trophoblasts by hypoxia or chemicals known to hinder cell differentiation. We also identify FGFR1 as a direct target of miR-424 in human trophoblasts. This effect is unique to miR-424 and is not seen with other members of this miRNA family that are expressed in trophoblasts, such as miR-15 and miR-16. Our findings establish a unique role for miR-424 during differentiation of human trophoblasts.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available