Effects of intrauterine extracellular vesicle microRNAs on embryonic gene expression in low-fertility cows

FASEB J. 2024 Oct 31;38(20):e70116. doi: 10.1096/fj.202401728R.

Abstract

Embryo survival and pre-implantation development depend on uterine luminal fluid, which is believed to play a role in early embryonic death and infertility in cows. Extracellular vesicles (EVs) in the uterine luminal fluid contain microRNAs (miRNAs), crucial mediators of intercellular communication. miRNAs regulate conceptus-maternal interactions and participate in embryonic development by suppressing gene expression. Therefore, we hypothesized that miRNAs in the intrauterine EVs of low-fertility cows would hinder embryonic survival and development. EVs were collected from the bovine uterine luminal fluid of both normal- and low-fertility cows 7 days post-estrus. Small RNA-sequencing analysis of miRNAs isolated from these EVs identified eight miRNAs that were highly expressed in normal-fertility cows (normal-fertility miRNAs) and eight with elevated expression in low-fertility cows (low-fertility miRNAs). These two sets of miRNAs were transfected into hatched blastocysts via lipofection. RNA-seq following lipofection with low-fertility miRNAs identified 424 differentially expressed genes (DEGs) relative to the control; in contrast, following lipofection with normal-fertility miRNAs, seven DEGs were identified. Pathway analysis of the DEGs identified following lipofection with low-fertility miRNAs revealed substantial enrichment of mitogen-activated protein kinase (MAPK) signaling. Expression of activator protein 1 (AP1) and interferon-tau (IFNT) mRNA was significantly lower in the low-fertility miRNA transfection group than in the control. IFNT is essential for maternal pregnancy recognition. Therefore, miRNAs in intrauterine EVs from low-fertility cows at 7 days post-estrus may inhibit embryo development and suppress IFNT expression by altering MAPK signaling.

Keywords: cow; extracellular vesicle; low‐fertility; microRNA; uterus.

MeSH terms

  • Animals
  • Blastocyst / metabolism
  • Cattle
  • Embryo, Mammalian / metabolism
  • Embryonic Development / genetics
  • Extracellular Vesicles* / metabolism
  • Female
  • Fertility / genetics
  • Gene Expression Regulation, Developmental
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Pregnancy
  • Pregnancy Proteins / genetics
  • Pregnancy Proteins / metabolism
  • Uterus / metabolism

Substances

  • MicroRNAs
  • Pregnancy Proteins