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DMT1 as a candidate for non‐transferrin‐bound iron uptake in the peripheral nervous system
Author(s) -
Vivot Rocio Martínez,
Goitia Belén,
Usach Vanina,
SettonAvruj Patricia C.
Publication year - 2013
Publication title -
biofactors
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.204
H-Index - 94
eISSN - 1872-8081
pISSN - 0951-6433
DOI - 10.1002/biof.1088
Subject(s) - dmt1 , transferrin , colocalization , myelin , ferritin , microbiology and biotechnology , western blot , peripheral nervous system , transferrin receptor , transporter , chemistry , context (archaeology) , biology , biochemistry , central nervous system , endocrinology , gene , paleontology
Iron, either in its chelated form or as holotransferrin (hTf), prevents the dedifferentiation of Schwann cells (SC), cells responsible for the myelination of the peripheral nervous system (PNS). This dedifferentiation is promoted by serum deprivation through cAMP release, PKA activation, and CREB phosphorylation. Since iron elicits its effect in a transferrin (Tf)‐free environment, in this work we postulate that non‐transferrin‐bound iron (NTBI) uptake must be involved. Divalent metal transporter 1(DMT1) has been widely described in literature as a key player in iron metabolism, but never before in the PNS context. The presence of DMT1 was demonstrated in nerve homogenate, isolated adult‐rat myelin, and cultured SC by Western Blot (WB) analysis and confirmed through its colocalization with S‐100β (SC marker) by immunocytochemical and immunohistochemical analyses. Furthermore, the existence of its mRNA was verified in sciatic nerve homogenate by RT‐PCR and throughout SC maturational stages. Finally, we describe DMT1′s subcellular location in the plasma membrane by confocal microscopy of SC and WB of different subcellular fractions. These data allow us to suggest the participation of DMT1 as part of a Tf independent iron uptake mechanism in SC and lead us to postulate a crucial role for iron in SC maturation and, as a consequence, in PNS myelination. © 2013 BioFactors, 39(4):476–484, 2013