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Survival, development, and electrical activity of central nervous system myelinated axons exposed to tumor necrosis factor in vitro
Author(s) -
DugandžijaNovaković S.,
Shrager Peter
Publication year - 1995
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.490400113
Subject(s) - myelin , tumor necrosis factor alpha , oligodendrocyte , central nervous system , biology , chemistry , microbiology and biotechnology , biophysics , neuroscience , endocrinology
Abstract Spinal cord explants from CD‐1 mouse embryos were cultured in Maximow slide assemblies to promote myelin development. At about 20 days in vitro, recombinant human or mouse tumor necrosis factor alpha (TNFa) was added. Observed 3–8 days later, myelin was largely intact. The myelin blistering and oligodendrocyte damage seen in other strains were generally absent. Axonal conduction was measured optically through the use of a voltage‐sensitive dye. Action potential shape, conduction velocity, and refractory period were all unchanged by exposure to TNFa. Two series of explants were grown with TNFa present continuously throughout the culture period. Observed with light and electron microscopy, myelin developed in at least 50% of the explants treated with recombinant mouse TNFα and 80% of those exposed to recombinant human TNFα. Optically recorded action potentials were of normal shape and refractory period. Conduction velocities were slightly lower than controls. CD‐1 mouse central nervous system contains TNFα receptors and yet was resistant to myelin damage. The apparent strain specificity of TNFα disruption of myelin may result from more indirect modes of action, including interaction with other cytokines produced by glial cells. Survival of axonal conduction suggest that Na + channel function remains intact following TNFα exposure. © 1995 Wiley‐Liss, Inc.