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      Metabolism-related microRNAs in maternal breast milk are influenced by premature delivery

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          Abstract

          Background

          Maternal breast milk (MBM) is enriched in microRNAs, factors that regulate protein translation throughout the human body. MBM from mothers of term and preterm infants differ in nutrient, hormone, and bioactive factor composition, but the microRNA differences between these groups have not been compared. We hypothesized that gestational age at delivery influences microRNA in MBM, particularly microRNAs involved in immunologic and metabolic regulation.

          Methods

          MBM from mothers of premature infants (pMBM) obtained 3–4 weeks post-delivery was compared with MBM from mothers of term infants obtained at birth (tColostrum) and 3–4 weeks post-delivery (tMBM). The microRNA profile in lipid and skim fractions of each sample was evaluated with high-throughput sequencing.

          Results

          The expression profiles of nine microRNAs in lipid and skim pMBM differed from tMBM. Gene targets of these microRNAs were functionally related to elemental metabolism and lipid biosynthesis. The microRNA profile of tColostrum was also distinct from pMBM, but clustered closely with tMBM. Twenty-one microRNAs correlated with gestational age demonstrated limited relationships with method of delivery, but not other maternal infant factors.

          Conclusion

          Premature delivery results in a unique MBM microRNA profile with metabolic targets. This suggests preterm milk may have adaptive functions for growth in premature infants.

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          Most cited references30

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          Effect of the INSIGHT Responsive Parenting Intervention on Rapid Infant Weight Gain and Overweight Status at Age 1 Year: A Randomized Clinical Trial.

          Rapid infant weight gain is associated with later obesity, but interventions to prevent rapid infant growth and reduce risk for overweight status in infancy are lacking.
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            Is Open Access

            Human milk miRNAs primarily originate from the mammary gland resulting in unique miRNA profiles of fractionated milk

            Human milk (HM) contains regulatory biomolecules including miRNAs, the origin and functional significance of which are still undetermined. We used TaqMan OpenArrays to profile 681 mature miRNAs in HM cells and fat, and compared them with maternal peripheral blood mononuclear cells (PBMCs) and plasma, and bovine and soy infant formulae. HM cells and PBMCs (292 and 345 miRNAs, respectively) had higher miRNA content than HM fat and plasma (242 and 219 miRNAs, respectively) (p < 0.05). A strong association in miRNA profiles was found between HM cells and fat, whilst PBMCs and plasma were distinctly different to HM, displaying marked inter-individual variation. Considering the dominance of epithelial cells in mature milk of healthy women, these results suggest that HM miRNAs primarily originate from the mammary epithelium, whilst the maternal circulation may have a smaller contribution. Our findings demonstrate that unlike infant formulae, which contained very few human miRNA, HM is a rich source of lactation-specific miRNA, which could be used as biomarkers of the performance and health status of the lactating mammary gland. Given the recently identified stability, uptake and functionality of food- and milk-derived miRNA in vivo, HM miRNA are likely to contribute to infant protection and development.
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              • Record: found
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              The role of TNF alpha in adipocyte metabolism.

              Tumor necrosis factor-alpha (TNF alpha) is a multifunctional cytokine which exerts a myriad of biological actions in different tissues and species. Many of these actions can perturb the normal regulation of energy metabolism. In adipose tissue, in particular, TNF alpha has been demonstrated to regulate or interfere with adipocyte metabolism at numerous sites including transcriptional regulation, glucose and fatty acid metabolism and hormone receptor signaling. The implications of these perturbations in disease states and the current understanding of the molecular mechanisms utilised by TNF alpha are discussed herein.
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                Author and article information

                Journal
                0100714
                6400
                Pediatr Res
                Pediatr. Res.
                Pediatric research
                0031-3998
                1530-0447
                18 March 2017
                24 May 2017
                August 2017
                24 November 2017
                : 82
                : 2
                : 226-236
                Affiliations
                [1 ]Franklin and Marshall College, Lancaster, PA
                [2 ]Department of Pediatrics, Penn State College of Medicine, Hershey, PA
                [3 ]Department of Biochemistry and Molecular Biology, Penn State College of Medicine, Hershey, PA
                [4 ]Department of Foods and Nutrition, University of Georgia, Athens, GA
                [5 ]Department of Cellular and Molecular Physiology, Penn State College of Medicine, Hershey, PA
                [6 ]Department of Pharmacology, Penn State College of Medicine, Hershey, PA
                [7 ]Department of Surgery, Penn State College of Medicine, Hershey, PA
                [8 ]Department of Public Health Sciences, Penn State College of Medicine, Hershey PA
                Author notes
                Corresponding author: Steven D. Hicks, Penn State College of Medicine, Department of Pediatrics, Mail Code HS83, 500 University Drive, PO Box 850, Hershey, PA 17033 0850, 717 531 8006, shicks1@ 123456hmc.psu.edu
                Article
                NIHMS855277
                10.1038/pr.2017.54
                5552431
                28422941
                e9197993-e937-462a-a8ee-69515e50b625

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                Pediatrics
                Pediatrics

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