Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0019158 (
hepatitis
)
30,205
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Myelin transcription factor 1
(
Myt1
) is a zinc-finger DNA binding protein that influences developing oligodendrocyte progenitor (OP) cell proliferation, differentiation, and myelin gene transcription in vitro. The potential of
Myt1
to play a role in OP responses leading to remyelination was examined using murine
hepatitis
virus strain A59 (MHV) to induce spinal cord demyelination and potential relevance to human pathology was evaluated in multiple sclerosis (MS) lesions. In MHV-infected mice, the density of
Myt1
expressing cells markedly increased in lesioned areas of spinal cord white matter.
Myt1
expressing cells proliferated most extensively during active demyelination and subsequently accumulated to maximal levels during early remyelination. Cells with nuclear
Myt1
immunoreactivity were mainly OP cells, identified by co-localization with platelet-derived growth factor alpha receptor, with additional phenotypes being either oligodendrocytes or neural stem cells, identified by CC1 antigen and Musashi1, respectively. The density of OP cells expressing
Myt1
was significantly increased in white matter of MHV-infected mice during demyelination and early remyelination then as remyelination advanced the values returned to levels comparable to PBS-injected control mice. In MHV lesions,
Myt1
was not expressed in astrocytes, lymphocytes, or macrophage/microglial cells. MS lesions demonstrated increased
Myt1
expression in both the periplaque white matter adjacent to lesions and within early remyelinating lesions. These results suggesta potential role for
Myt1
in the regeneration of oligodendrocyte lineage cells in response to demyelination.
...
PMID:Myelin transcription factor 1 (Myt1) expression in demyelinated lesions of rodent and human CNS. 1733 Aug 75