Abstract

LIN28 inhibits let-7 miRNA maturation which prevents cell differentiation and promotes proliferation. We hypothesized that the LIN28-let-7 axis regulates proliferation-associated genes in sheep trophectoderm in vivo. Day 9-hatched sheep blastocysts were incubated with lentiviral particles to deliver shRNA targeting LIN28 specifically to trophectoderm cells. At day 16, conceptus elongation was significantly reduced in LIN28A and LIN28B knockdowns. Let-7 miRNAs were significantly increased and IGF2BP1-3, HMGA1, ARID3B, and c-MYC were decreased in trophectoderm from knockdown conceptuses. Ovine trophoblast (OTR) cells derived from day 16 trophectoderm are a useful tool for in vitro experiments. Surprisingly, LIN28 was significantly reduced and let-7 miRNAs increased after only a few passages of OTR cells, suggesting these passaged cells represent a more differentiated phenotype. To create an OTR cell line more similar to day 16 trophectoderm we overexpressed LIN28A and LIN28B, which significantly decreased let-7 miRNAs and increased IGF2BP1-3, HMGA1, ARID3B, and c-MYC compared to control. This is the first study showing the role of the LIN28-let-7 axis in trophoblast proliferation and conceptus elongation in vivo. These results suggest that reduced LIN28 during early placental development can lead to reduced trophoblast proliferation and sheep conceptus elongation at a critical period for successful establishment of pregnancy.

Highlights

  • Placental development is one of the main factors determining perinatal fetal growth and postnatal fetal and maternal health

  • LIN28A mRNA and protein was significantly reduced in AKD TE while LIN28B mRNA and protein was significantly reduced in BKD TE compared to SC (Figure 1A,B)

  • These results suggest that reduced LIN28A or LIN28B led to significant increase in let-7 miRNAs

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Summary

Introduction

Placental development is one of the main factors determining perinatal fetal growth and postnatal fetal and maternal health. If the balance between proliferation and differentiation of CTBs is dysregulated, it can result in severe disorders including preterm birth, intrauterine growth restriction (IUGR), and preeclampsia [3,4]. These pregnancy related disorders affect about a third of human pregnancies [5]. Exploring the genes involved in sheep trophectoderm elongation can help to better understand the reasons for reduced fertility in domestic ruminants and to improve the diagnosis and treatment of various pregnancy-related disorders in humans

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