Longitudinal Human Milk miRNA Composition over the First 3 mo of Lactation in a Cohort of Healthy Mothers Delivering Term Infants

Author:

Raymond Frederic1,Lefebvre Gregory1,Texari Lorane1,Pruvost Solenn1,Metairon Sylviane1,Cottenet Geoffrey1,Zollinger Alix1,Mateescu Bogdan2,Billeaud Claude3,Picaud Jean-Charles45,Silva-Zolezzi Irma6,Descombes Patrick1,Bosco Nabil16ORCID

Affiliation:

1. Nestlé Research, Société des Produits Nestlé S.A., Lausanne, Switzerland

2. Brain Research Institute, University of Zurich, Zurich, Switzerland

3. Neonatology Nutrition, Lactarium Bordeaux-Marmande, Bordeaux, France

4. Neonatal Intensive Care Unit, University Hospital Croix Rousse, Lyon, France

5. CarMeN unit, Claude Bernard University Lyon 1, 69310 Pierre Benite, France

6. Nestlé Research, Singapore

Abstract

ABSTRACT Background MicroRNAs (miRNAs) are small noncoding RNAs involved in posttranscriptional regulation. miRNAs can be secreted and found in many body fluids, and although they are particularly abundant in breastmilk, their functions remain elusive. Human milk (HM) miRNAs start to raise considerable interest, but a comprehensive understanding of the repertoire and expression profiles along lactation has not been well characterized. Objectives This study aimed to characterize the longitudinal profile of HM miRNA between the second week and third month postpartum. Methods We used a new sensitive technology to measure HM miRNAs in a cohort of 44 French mothers [mean ± SD age: 31 ± 3.5; BMI (in kg/m2) 21.8 ± 2.3] who delivered at term and provided HM samples at 3 time points (17 ± 3 d, 60 ± 3 d, and 90 ± 3 d) during follow-up visits. Results We detected 685 miRNAs, of which 35 showed a high and stable expression along the lactation period analyzed. We also described for the first time a set of 11 miRNAs with a dynamic expression profile. To gain insight into the potential functional relevance of this set of miRNAs, we selected miR-3126 and miR-3184 to treat undifferentiated Caco-2 human intestinal cells and then assessed differentially expressed genes and modulation of related biological pathways. Conclusions Overall, our study provides new insights into HM miRNA composition and, to our knowledge, the first description of its longitudinal dynamics in mothers who delivered at term. Our in vitro results obtained in undifferentiated Caco-2 human intestinal cells transfected with HM miRNAs also provide further support to the hypothesized mother-to-neonate signaling role of HM miRNAs. This trial was registered at clinicaltrials.gov as NCT01894893.

Publisher

Oxford University Press (OUP)

Subject

Nutrition and Dietetics,Medicine (miscellaneous)

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