Abstract
Human milk plays a significant role in postnatal gut maturation and may serve as a vehicle for transmitting developmental signals from mother to neonate (Okada et al. 1991; Wagner et al. 1995). Various growth factors, cytokines, and gut peptides have been isolated from human milk, often in quantities that exceed maternal serum levels (Kudlow & Bjorge 1990; Coffey et al. 1992). There exists an interrelated system in which compartmentation of milk components leads to controlled release of nutrients and metabolites to the breastfed infant. Various proteins are sequestered differentially within the compartments of human milk. These proteins become sequentially processed within the gastrointestinal tract (Kudlow & Bjorge 1990). The majority of studies on human milk have focused on the aqueous (defatted) fraction of whole milk rather than the various compartments that include fat. Yet, the fat compartment composed of the milk fat globule with its associated plasma membrane appears to provide a unique delivery system of bioactive substances to the newborn gut (Okada et al. 1991; Wagner et al. 1995; Jensen etal. 1995).
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References
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Wagner CL, Baatz JA. Higher molecular mass forms of TGFa in human milk. In: Pickering LK, Morrow AL, Ruiz-Palacios GM, Schanler RJ. Protecting Infants through Human Milk: Advancing the Scientific Evidence. Advances in Experimental Medicine and Biology Series. New York: Kluwer Academic/Plenum Publishers, 2004; this volume.
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Wagner, C.L., Baatz, J.E. (2004). TGFα within Compartments of Human Milk. In: Pickering, L.K., Morrow, A.L., Ruiz-Palacios, G.M., Schanler, R.J. (eds) Protecting Infants through Human Milk. Advances in Experimental Medicine and Biology, vol 554. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-4242-8_54
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DOI: https://doi.org/10.1007/978-1-4757-4242-8_54
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