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1.
Glia ; 59(10): 1529-39, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21656857

ABSTRACT

Recently, we showed that Schwann cells transfer ribosomes to injured axons. Here, we demonstrate that Schwann cells transfer ribosomes to regenerating axons in vivo. For this, we used lentiviral vector-mediated expression of ribosomal protein L4 and eGFP to label ribosomes in Schwann cells. Two approaches were followed. First, we transduced Schwann cells in vivo in the distal trunk of the sciatic nerve after a nerve crush. Seven days after the crush, 12% of regenerating axons contained fluorescent ribosomes. Second, we transduced Schwann cells in vitro that were subsequently injected into an acellular nerve graft that was inserted into the sciatic nerve. Fluorescent ribosomes were detected in regenerating axons up to 8 weeks after graft insertion. Together, these data indicate that regenerating axons receive ribosomes from Schwann cells and, furthermore, that Schwann cells may support local axonal protein synthesis by transferring protein synthetic machinery and mRNAs to these axons.


Subject(s)
Axons/physiology , Nerve Regeneration/physiology , Ribosomes/metabolism , Schwann Cells/ultrastructure , Sciatic Neuropathy/surgery , Animals , Axons/metabolism , Axons/pathology , Biological Transport/physiology , Functional Laterality , Green Fluorescent Proteins/genetics , Green Fluorescent Proteins/metabolism , Male , Mice , Mice, Inbred C57BL , Microscopy, Electron, Transmission , Nerve Crush/methods , Neurofilament Proteins/metabolism , Rats , Rats, Inbred Lew , Ribosomes/ultrastructure , Schwann Cells/pathology , Schwann Cells/transplantation , Sciatic Neuropathy/etiology , Time Factors , Transduction, Genetic/methods
2.
J Neurosci ; 28(43): 11024-9, 2008 Oct 22.
Article in English | MEDLINE | ID: mdl-18945910

ABSTRACT

Schwann cells play pivotal roles in the development and maintenance of the peripheral nervous system. Here, we show that intact sciatic nerve axons of mice contain a small population of ribosomes, which increases by several orders of magnitude when axons are desomatized (severed from their cell bodies). We furthermore demonstrate, using the Wallerian degeneration slow mouse as a model, that Schwann cells transfer polyribosomes to desomatized axons. These data indicate that Schwann cells have the propensity to control axonal protein synthesis by supplying ribosomes on local basis.


Subject(s)
Axons/physiology , Neuroglia/cytology , Ribosomes/metabolism , Schwann Cells/physiology , Animals , Axons/ultrastructure , Biological Transport/genetics , Disease Models, Animal , Green Fluorescent Proteins/genetics , Green Fluorescent Proteins/metabolism , Mice , Mice, Inbred C57BL , Mice, Mutant Strains , Microscopy, Electron, Transmission/methods , Myelin Basic Protein/metabolism , Myelin P0 Protein/metabolism , Nerve Tissue Proteins/genetics , Neuroglia/physiology , Polyribosomes/metabolism , Sciatic Neuropathy/genetics , Sciatic Neuropathy/pathology , Sciatic Neuropathy/physiopathology , Transfection/methods
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