The human placenta is required to be the anchor, the conduit and the controller during pregnancy. The survival of the baby and its associated placenta is dependent upon the placenta shielding the embryo/fetus from harm, e.g., autoimmune disease -thrombophilia, antiphospholipid syndrome or infections, while simultaneously providing for the passage of critical nutrients (e.g., amino acids, vitamins) and beneficial immunoglobulins. In a number of instances, the movements of macromolecules into and through the placenta can result in the passage of the intact molecules into the fetal circulation or in the case of proteins -catabolism to amino acids which are utilized by the placenta and the fetus for continued growth and development. The transfer of two such macromolecules, immunoglobulin G (IgG) and vitamin B12 (cyanocobalamin or B12), are examined as to the unique receptor-mediated transfer capability of the human placenta, its transfer specificity as related to specific receptors and the role of endogeneous placental proteins (trancobalamins) in facilitating the recognition and transport of specifically B12. Brief comparisons will be made to other animal species and the differences in specific organ transfer capabilities.
KEY WORDS: immunoglobulin IgG, transcobalamin, vitamin B12, placental transport, human
Overview of macromolecule transport and catabolism by the placenta and extraembryonic membranes in different speciesThe development of the embryo and fetus is dependent upon the function of the placenta and its extraembryonic membranes in every mammalian species. Of significance is the interdependence of theses extraembryonic tissues in maintaining the conceptus and allowing for normal development.Across species, macromolecules play multiple roles in providing for this development. In particular, the transport physiologists and membrane biochemist focus on the transporters and the transcytosis that occurs for immuno-regulators and essential vitamins for normal development. Yet even the basic building blocks created by the degradation of these macromolecules provide for the growth of both fetus and placenta. The large contribution of amino acids from the metabolism of proteins, e.g., maternal albumin and other circulating proteins, provide the large Int.