Breast Milk-Derived Biomolecules in Human Health

A special issue of Biomolecules (ISSN 2218-273X). This special issue belongs to the section "Cellular Biochemistry".

Deadline for manuscript submissions: closed (30 November 2021) | Viewed by 22335

Special Issue Editor


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Guest Editor
1. Institute of Neurobiology, Ulm University, 89081 Ulm, Germany
2. Children's Hospital and Institute of Pediatrics, University of Debrecen, Nagyerdei krt. 98, 4032 Debrecen, Hungary
Interests: comparative molecular endocrinology; immunometabolism; metabolic biochemistry; inflammation and innate immunity; macrophage biology; functional genomics of diabetes and obesity

Special Issue Information

Dear Colleagues,

The multiplicity of benefits of breastfeeding have now been established. In addition to being the best source of nutrition for infants, breast milk confers important and lasting infant and maternal health benefits. A richer understanding of the health impact of the many biomolecules present in breast milk should have far reaching societal benefits. Maternal biomolecules establish a fascinating mother-to-child signaling through breastfeeding. Breast milk antibodies, cytokines, and other immune molecules ensure disease immunity, protect the developing intestinal barrier from inflammation, and reduce the risk of chronic inflammatory diseases. The hormones, cytokines, lipids, vitamins, and oligosaccharides in breast milk control organ differentiation, thermogenesis, cognitive development, and the growth of normal flora. Insufficient breastfeeding promotes childhood obesity and increases the risk of inflammatory diseases and diabetes in later life [1–8]. However, the rate of breastfeeding has declined dramatically, with a possible negative impact on infant and adolescent health [4,9]. Understanding the health impact of both breast and formula milk biomolecules is hence timely and important. The topics of this Special Issue include, but are not limited to, studies on the biomolecules of the milk microbiome; the impact of milk biomolecules on the gut–brain–immune axis; obesogens in breast milk; neurotransmitters, hormones, and cytokines in breast milk; extracellular vesicles and cells in breast milk; the impact of maternal health on milk quality; clinical studies dealing with the health impacts of formula-feeding and breastfeeding. Original research articles, technical notes, case reports, short reviews, and commentaries are welcome. As the Guest Editor of this Special Issue, I hope that the collection of articles will be useful references for teaching and research to stimulate discussion and to open up new avenues of research, and will be situated within the existing literature as a reference point.

References:

  1. Stewart, C.J.; Ajami, N.J.; O’Brien, J.L.; Hutchinson, D.S.; Smith, D.P.; Wong, M.C.; Ross, M.C.; Lloyd, R.E.; Doddapaneni, H.; Metcalf, G.A.; et al. Temporal development of the gut microbiome in early childhood from the TEDDY study. Nature 2018, 562, 583–588.
  2. Yu, H.; Dilbaz, S.; Coßmann, J.; Hoang, A.C.; Diedrich, V.; Herwig, A.; Harauma, A.; Hoshi, Y.; Moriguchi, T.; Landgraf, K.; et al. Breast milk alkylglycerols sustain beige adipocytes through adipose tissue macrophages. J. Clin. Investig. 2019, 129, 2485–2499.
  3. Liang, G.; Zhao, C.; Zhang, H.; Mattei, L.; Sherrill-Mix, S.; Bittinger, K.; Kessler, L.R.; Wu, G.D.; Baldassano, R.N.; DeRusso, P.; et al. The stepwise assembly of the neonatal virome is modulated by breastfeeding. Nature 2020, 581, 470–474.
  4. Pietrobelli, A.; Agosti, M.; the MeNu Group. Nutrition in the First 1000 Days: Ten Practices to Minimize Obesity Emerging from Published Science. Int. J. Environ. Res. Public Health 2017, 14, 1491.
  5. Melnik, B.C.; John, S.M.; Schmitz, G.; Milk is not just food but most likely a genetic transfection system activating mTORC1 signaling for postnatal growth. Nutr. J. 2013, 12, 103.
  6. Savino, F.; Fissore, M.F.; Liguori, S.A.; Oggero, R. Can hormones contained in mothers' milk account for the beneficial effect of breast-feeding on obesity in children? Clin. Endocrinol. 2009, 71, 757–765.
  7. Sodhi, C.P.; Wipf, P.; Yamaguchi, Y.; Fulton, W.B.; Kovler, M.; Niño, D.F.; Zhou, Q.; Banfield, E.; Werts, A.D.; Ladd, M.R.; et al. The human milk oligosaccharides 2’-fucosyllactose and 6’-sialyllactose protect against the development of necrotizing enterocolitis by inhibiting toll-like receptor 4 signaling. Pediatric Res. 2020.
  8. Bardanzellu, F.; Fanos, V.; Reali, A. "Omics" in Human Colostrum and Mature Milk: Looking to Old Data with New Eyes. Nutrients 2017, 9, 843.
  9. Grummer‐Strawn, L.M.; Zehner, E.; Stahlhofer, M.; Lutter, C.; Clark, D.; Sterken, E.; Harutyunyan, S.; Ransom, E.I.; WHO/UNICEF NetCode. New World Health Organization guidance helps protect breastfeeding as a human right. Matern. Child Nutr. 2017, 13, e12491.

Dr. Tamás Röszer
Guest Editor

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Keywords

  • metabolism
  • immunology
  • nutrition
  • endocrinology
  • breastfeeding
  • neonate care

Published Papers (5 papers)

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Editorial

Jump to: Review

3 pages, 656 KiB  
Editorial
Mother-to-Child Signaling through Breast Milk Biomolecules
by Tamás Röszer
Biomolecules 2021, 11(12), 1743; https://doi.org/10.3390/biom11121743 - 23 Nov 2021
Cited by 7 | Viewed by 2028
Abstract
Breastfeeding—or lactation—is a unique and defining reproductive trait of mammals that nourishes offspring by supplying nutrient-rich breast milk [...] Full article
(This article belongs to the Special Issue Breast Milk-Derived Biomolecules in Human Health)
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Review

Jump to: Editorial

19 pages, 2572 KiB  
Review
Co-Evolution of Breast Milk Lipid Signaling and Thermogenic Adipose Tissue
by Tamás Röszer
Biomolecules 2021, 11(11), 1705; https://doi.org/10.3390/biom11111705 - 16 Nov 2021
Cited by 7 | Viewed by 3145
Abstract
Breastfeeding is a unique and defining behavior of mammals and has a fundamental role in nourishing offspring by supplying a lipid-rich product that is utilized to generate heat and metabolic fuel. Heat generation from lipids is a feature of newborn mammals and is [...] Read more.
Breastfeeding is a unique and defining behavior of mammals and has a fundamental role in nourishing offspring by supplying a lipid-rich product that is utilized to generate heat and metabolic fuel. Heat generation from lipids is a feature of newborn mammals and is mediated by the uncoupling of mitochondrial respiration in specific fat depots. Breastfeeding and thermogenic adipose tissue have a shared evolutionary history: both have evolved in the course of homeothermy evolution; breastfeeding mammals are termed “thermolipials”, meaning “animals with warm fat”. Beyond its heat-producing capacity, thermogenic adipose tissue is also necessary for proper lipid metabolism and determines adiposity in offspring. Recent advances have demonstrated that lipid metabolism in infants is orchestrated by breast milk lipid signals, which establish mother-to-child signaling and control metabolic development in the infant. Breastfeeding rates are declining worldwide, and are paralleled by an alarming increase in childhood obesity, which at least in part may have its roots in the impaired metabolic control by breast milk lipid signals. Full article
(This article belongs to the Special Issue Breast Milk-Derived Biomolecules in Human Health)
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47 pages, 14889 KiB  
Review
Exosome-Derived MicroRNAs of Human Milk and Their Effects on Infant Health and Development
by Bodo C. Melnik, Wolfgang Stremmel, Ralf Weiskirchen, Swen Malte John and Gerd Schmitz
Biomolecules 2021, 11(6), 851; https://doi.org/10.3390/biom11060851 - 7 Jun 2021
Cited by 85 | Viewed by 9392
Abstract
Multiple biologically active components of human milk support infant growth, health and development. Milk provides a wide spectrum of mammary epithelial cell-derived extracellular vesicles (MEVs) for the infant. Although the whole spectrum of MEVs appears to be of functional importance for the growing [...] Read more.
Multiple biologically active components of human milk support infant growth, health and development. Milk provides a wide spectrum of mammary epithelial cell-derived extracellular vesicles (MEVs) for the infant. Although the whole spectrum of MEVs appears to be of functional importance for the growing infant, the majority of recent studies report on the MEV subfraction of milk exosomes (MEX) and their miRNA cargo, which are in the focus of this review. MEX and the dominant miRNA-148a play a key role in intestinal maturation, barrier function and suppression of nuclear factor-κB (NF-κB) signaling and may thus be helpful for the prevention and treatment of necrotizing enterocolitis. MEX and their miRNAs reach the systemic circulation and may impact epigenetic programming of various organs including the liver, thymus, brain, pancreatic islets, beige, brown and white adipose tissue as well as bones. Translational evidence indicates that MEX and their miRNAs control the expression of global cellular regulators such as DNA methyltransferase 1—which is important for the up-regulation of developmental genes including insulin, insulin-like growth factor-1, α-synuclein and forkhead box P3—and receptor-interacting protein 140, which is important for the regulation of multiple nuclear receptors. MEX-derived miRNA-148a and miRNA-30b may stimulate the expression of uncoupling protein 1, the key inducer of thermogenesis converting white into beige/brown adipose tissue. MEX have to be considered as signalosomes derived from the maternal lactation genome emitted to promote growth, maturation, immunological and metabolic programming of the offspring. Deeper insights into milk’s molecular biology allow the conclusion that infants are both “breast-fed” and “breast-programmed”. In this regard, MEX miRNA-deficient artificial formula is not an adequate substitute for breastfeeding, the birthright of all mammals. Full article
(This article belongs to the Special Issue Breast Milk-Derived Biomolecules in Human Health)
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15 pages, 1827 KiB  
Review
Review of Methodological Approaches to Human Milk Small Extracellular Vesicle Proteomics
by Brett Vahkal, Jamie Kraft, Emanuela Ferretti, Minyoung Chung, Jean-François Beaulieu and Illimar Altosaar
Biomolecules 2021, 11(6), 833; https://doi.org/10.3390/biom11060833 - 3 Jun 2021
Cited by 8 | Viewed by 3615
Abstract
Proteomics can map extracellular vesicles (EVs), including exosomes, across disease states between organisms and cell types. Due to the diverse origin and cargo of EVs, tailoring methodological and analytical techniques can support the reproducibility of results. Proteomics scans are sensitive to in-sample contaminants, [...] Read more.
Proteomics can map extracellular vesicles (EVs), including exosomes, across disease states between organisms and cell types. Due to the diverse origin and cargo of EVs, tailoring methodological and analytical techniques can support the reproducibility of results. Proteomics scans are sensitive to in-sample contaminants, which can be retained during EV isolation procedures. Contaminants can also arise from the biological origin of exosomes, such as the lipid-rich environment in human milk. Human milk (HM) EVs and exosomes are emerging as a research interest in health and disease, though the experimental characterization and functional assays remain varied. Past studies of HM EV proteomes have used data-dependent acquisition methods for protein detection, however, improvements in data independent acquisition could allow for previously undetected EV proteins to be identified by mass spectrometry. Depending on the research question, only a specific population of proteins can be compared and measured using isotope and other labelling techniques. In this review, we summarize published HM EV proteomics protocols and suggest a methodological workflow with the end-goal of effective and reproducible analysis of human milk EV proteomes. Full article
(This article belongs to the Special Issue Breast Milk-Derived Biomolecules in Human Health)
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14 pages, 2633 KiB  
Review
Anti-Angiogenic Property of Free Human Oligosaccharides
by Boram Bae, Haeun Kim, Hyerin Park, Young Jun Koh, Sung-Jin Bae and Ki-Tae Ha
Biomolecules 2021, 11(6), 775; https://doi.org/10.3390/biom11060775 - 21 May 2021
Cited by 4 | Viewed by 2612
Abstract
Angiogenesis, a fundamental process in human physiology and pathology, has attracted considerable attention owing to its potential as a therapeutic strategy. Vascular endothelial growth factor (VEGF) and its receptor (VEGFR) are deemed major mediators of angiogenesis. To date, inhibition of the VEGF-A/VEGFR-2 axis [...] Read more.
Angiogenesis, a fundamental process in human physiology and pathology, has attracted considerable attention owing to its potential as a therapeutic strategy. Vascular endothelial growth factor (VEGF) and its receptor (VEGFR) are deemed major mediators of angiogenesis. To date, inhibition of the VEGF-A/VEGFR-2 axis has been an effective strategy employed in the development of anticancer drugs. However, some limitations, such as low efficacy and side effects, need to be addressed. Several drug candidates have been discovered, including small molecule compounds, recombinant proteins, and oligosaccharides. In this review, we focus on human oligosaccharides as modulators of angiogenesis. In particular, sialylated human milk oligosaccharides (HMOs) play a significant role in the inhibition of VEGFR-2-mediated angiogenesis. We discuss the structural features concerning the interaction between sialylated HMOs and VEGFR-2 as a molecular mechanism of anti-angiogenesis modulation and its effectiveness in vivo experiments. In the current state, extensive clinical trials are required to develop a novel VEGFR-2 inhibitor from sialylated HMOs. Full article
(This article belongs to the Special Issue Breast Milk-Derived Biomolecules in Human Health)
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