No effect of an elevated miR-30b level in mouse milk on its level in pup tissues

Johann Laubier1, Johan Castille, Sandrine Le Guillou

  • 1a INRA; UMR1313 Génétique Animale et Biologie Intégrative ; Jouy-en-Josas , France.

RNA Biology
|March 13, 2015
PubMed

Insights

Ingested microRNAs are not transferred to tissues in pups, even with high levels in milk. This study found no evidence of horizontal microRNA delivery via oral ingestion in a mouse model.

Area of Science:

  • Molecular Biology
  • Genetics
  • Developmental Biology

Background:

  • Recent reports suggest ingested microRNAs can transfer to blood and tissues, regulating gene expression.
  • Replication of these findings has been inconsistent, raising questions about microRNA bioavailability and function after ingestion.

Purpose of the Study:

  • To investigate the horizontal delivery of microRNAs from mother's milk to pups via oral ingestion.
  • To determine if high levels of microRNA in milk lead to its accumulation in pup tissues.

Main Methods:

  • Utilized a transgenic mouse model engineered to express high levels of miR-30b in milk.
  • Administered milk from transgenic mothers to pups and compared tissue microRNA levels with pups fed by wild-type mothers.
  • Quantified miR-30b levels in milk, stomach contents, and various pup tissues.

Main Results:

  • Very high concentrations of miR-30b were detected in the milk of transgenic females and in the stomach contents of their pups.
  • No significant increase in miR-30b levels was observed in the tissues of pups fed milk from transgenic mothers compared to controls.
  • This suggests that oral ingestion of microRNAs does not lead to systemic transfer or tissue accumulation in this model.

Conclusions:

  • Horizontal transfer of microRNAs from ingested milk to pup tissues is not supported by this study.
  • High dietary intake of microRNAs does not necessarily result in their functional presence in target tissues.
  • Further research is needed to understand the fate and potential biological impact of ingested microRNAs.

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