Abstract / Description of output
The molecular events that occur at the early phase of many demyelinating neurodegenerative diseases are unknown. A recent demonstration of rapid demyelination and axonal injury induced by Mycobacterium leprae provides a model for elucidating the molecular events of early nerve degeneration which might be common to neurodegenerative diseases of both infectious origin and unknown etiology. The identification of the M. leprae-targeted Schwann cell receptor, dystroglycan, and its associated molecules in myelination, demyelination and axonal functions suggests a role for these molecules in early nerve degeneration.
Original language | English |
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Pages (from-to) | 511-518 |
Number of pages | 8 |
Journal | Current Opinion in Immunology |
Volume | 16 |
Issue number | 4 |
DOIs | |
Publication status | Published - 1 Aug 2004 |
Keywords / Materials (for Non-textual outputs)
- central nervous system
- CNS
- DRP2
- dystroglycan-related protein 2
- G
- GBS
- globular
- Guillain-Barre syndrome
- LCMV
- lepromatous leprosy
- LL
- lymphocytic choriomeningitis virus
- MS
- multiple sclerosis
- peripheral nervous system
- PGL-1
- phenolic glycolipid-1
- PNS