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Transferrin Is an Essential Factor for Myelination
Authors:A. Espinosa de los Monteros  S. Kumar  P. Zhao  C. J. Huang  R. Nazarian  T. Pan  S. Scully  R. Chang  J. de Vellis
Affiliation:(1) Mental Retardation Research Center, Departments of Neurobiology & Psychiatry, Brain Research Institute, UCLA School of Medicine, Los Angeles, CA;(2) UCLA Mental Retardation Research Center, 760 Westwood Plaza, 68-177 NPI, 90024-1759 Los Angeles, CA
Abstract:It has been established that oligodendrocytes, the myelin forming cells, participate in iron homeostasis through the synthesis and secretion of transferrin. Here we investigated whether a correlation exists between myelination, the commonly studied function of oligodendrocytes, and that of transferrin synthesis and secretion. We used a proteolipid protein mutant, the myelin deficient rat, whose condition is characterized by severe hypomyelination. We compared the ontogenic profile for transferrin gene expression in mutants with that of unaffected rat pups through northern blot analysis and in situ hybridization. Surprisingly, transferrin synthesis was null in mutant oligodendrocytes. Next, we demonstrated that a single apo-transferrin intraparenchymal injection administered to P5 rat pups enabled mutant oligodendrocytes to synthesize myelin basic protein and to myelinate axons, indicating that transferrin effects mutant oligodendrocyte maturation regardless of its source. Thus, transferrin availability is essential for oligodendrocyte maturation and function, and oligodencrocytes are most vulnerable to transferrin deficiency during the premyelinating stage.
Keywords:Myelin  transferrin  oligodendrocytes  iron metabolism
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