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MicroRNAs in Breastmilk and the Lactating Breast: Potential Immunoprotectors and Developmental Regulators for the Infant and the Mother

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Publisher MDPI
Date 2015 Nov 4
PMID 26529003
Citations 107
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Abstract

Human milk (HM) is the optimal source of nutrition, protection and developmental programming for infants. It is species-specific and consists of various bioactive components, including microRNAs, small non-coding RNAs regulating gene expression at the post-transcriptional level. microRNAs are both intra- and extra-cellular and are present in body fluids of humans and animals. Of these body fluids, HM appears to be one of the richest sources of microRNA, which are highly conserved in its different fractions, with milk cells containing more microRNAs than milk lipids, followed by skim milk. Potential effects of exogenous food-derived microRNAs on gene expression have been demonstrated, together with the stability of milk-derived microRNAs in the gastrointestinal tract. Taken together, these strongly support the notion that milk microRNAs enter the systemic circulation of the HM fed infant and exert tissue-specific immunoprotective and developmental functions. This has initiated intensive research on the origin, fate and functional significance of milk microRNAs. Importantly, recent studies have provided evidence of endogenous synthesis of HM microRNA within the human lactating mammary epithelium. These findings will now form the basis for investigations of the role of microRNA in the epigenetic control of normal and aberrant mammary development, and particularly lactation performance.

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References
1.
Pauley K, Cha S, Chan E . MicroRNA in autoimmunity and autoimmune diseases. J Autoimmun. 2009; 32(3-4):189-94. PMC: 2717629. DOI: 10.1016/j.jaut.2009.02.012. View

2.
Lu L, Liston A . MicroRNA in the immune system, microRNA as an immune system. Immunology. 2009; 127(3):291-8. PMC: 2712098. DOI: 10.1111/j.1365-2567.2009.03092.x. View

3.
Vigorito E, Perks K, Abreu-Goodger C, Bunting S, Xiang Z, Kohlhaas S . microRNA-155 regulates the generation of immunoglobulin class-switched plasma cells. Immunity. 2007; 27(6):847-59. PMC: 4135426. DOI: 10.1016/j.immuni.2007.10.009. View

4.
Koralov S, Muljo S, Galler G, Krek A, Chakraborty T, Kanellopoulou C . Dicer ablation affects antibody diversity and cell survival in the B lymphocyte lineage. Cell. 2008; 132(5):860-74. DOI: 10.1016/j.cell.2008.02.020. View

5.
Brabletz T, Jung A, Hlubek F, Lohberg C, Meiler J, Suchy U . Negative regulation of CD4 expression in T cells by the transcriptional repressor ZEB. Int Immunol. 1999; 11(10):1701-8. DOI: 10.1093/intimm/11.10.1701. View