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High serum levels of BMP-2 correlate with BMP-4 and BMP-5 levels and induce reduced neuronal phenotype in patients with relapsing-remitting multiple sclerosis
- Source :
- Journal of Neuroimmunology. 310:120-128
- Publication Year :
- 2017
- Publisher :
- Elsevier BV, 2017.
-
Abstract
- Blockage of bone morphogenetic protein (BMP) signaling is required for differentiation of neurons and oligodendrocytes from neural stem cells (NSCs). Sera of untreated relapsing-remitting multiple sclerosis (RR-MS) patients expressed significantly higher levels of BMP-2 compared to sera of healthy controls. BMP-2 levels correlated with BMP-4 and -5 levels only in sera of untreated MS patients. Furthermore, sera of untreated patients inhibited the neuronal differentiation of RA-treated P19 cells, which was associated with induction of phospho-SMAD signaling pathway. These results suggest that BMP-2 sera levels may play a role in the failure of remyelination and neuro-regeneration in RR-MS.
- Subjects :
- Adult
Male
0301 basic medicine
medicine.medical_specialty
Adolescent
Statistics as Topic
Immunology
Bone Morphogenetic Protein 2
Enzyme-Linked Immunosorbent Assay
Smad Proteins
Bone Morphogenetic Protein 4
Bone Morphogenetic Protein 5
Biology
Bone morphogenetic protein
Bone morphogenetic protein 2
Disability Evaluation
Young Adult
03 medical and health sciences
Multiple Sclerosis, Relapsing-Remitting
Neural Stem Cells
Internal medicine
medicine
Humans
Immunology and Allergy
Remyelination
Multiple sclerosis
Neurogenesis
Interferon-beta
Middle Aged
medicine.disease
Neural stem cell
Oligodendroglia
030104 developmental biology
P19 cell
medicine.anatomical_structure
Endocrinology
Neurology
Bone morphogenetic protein 4
embryonic structures
Cytokines
Female
Neurology (clinical)
Signal Transduction
Subjects
Details
- ISSN :
- 01655728
- Volume :
- 310
- Database :
- OpenAIRE
- Journal :
- Journal of Neuroimmunology
- Accession number :
- edsair.doi.dedup.....93605acfff1eab68be4e62f59fbc7c4e
- Full Text :
- https://doi.org/10.1016/j.jneuroim.2017.07.008