Pathological investigations of tissue from multiple sclerosis (MS) and Guillain-Barre syndrome (GBS) patients have shown macrophages containing myeline debris in and around demyelinating lesions. In MS, GBS, and experimental inflammatory demyelination in animals, demyelination appears only to occur in the presence of macrophages. Ultrastructural studies suggest that macrophages become closely apposed to the myelin sheath and remove myelin from the axon. Demyelination in animal models can be delayed or reduced by treatment with agents that impair macrophage function. It is not clear, however, to what extent macrophages begin the process of demyelination, extend demyelination initiated by other mechanisms, or act as scavengers of previously damaged myelin sheaths. This project is designed to establish the degree of involvement of macrophages in the initiation, execution, and termination of the demyelinating process. This will be accomplished by examination of the interaction of functionally different populations of macrophages with a range of well-defined myelin preparations consisting of isolated myelin components, reconstituted myelin vesicles, and in vitro myelinating cultures. The investigations will include: 1) binding of macrophages to myelin, both directly and via intermediate ligands; 2) study of the effect of the nervous system environment on macrophage function; 3) study of the ability of endogenous and exogenous macrophages to demyelinate in vitro myelinating culture systems; and 4) application of these findings to the study of macrophages from animals with experimental demyelinating diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
1R01NS023121-01
Application #
3406276
Study Section
Neurology B Subcommittee 1 (NEUB)
Project Start
1986-01-01
Project End
1988-12-31
Budget Start
1986-01-01
Budget End
1986-12-31
Support Year
1
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
071723621
City
Boston
State
MA
Country
United States
Zip Code
02115
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Liu, Y; Peterson, D A; Kimura, H et al. (1997) Mechanism of cellular 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) reduction. J Neurochem 69:581-93
Peterson, D A; Leppert, J T; Lee, K F et al. (1997) Basal forebrain neuronal loss in mice lacking neurotrophin receptor p75. Science 277:837-9
Johnson, D; Seeldrayers, P A; Weiner, H L (1988) The role of mast cells in demyelination. 1. Myelin proteins are degraded by mast cell proteases and myelin basic protein and P2 can stimulate mast cell degranulation. Brain Res 444:195-8