共 40 条
Exosome-enriched fractions from MS B cells induce oligodendrocyte death
被引:33
作者:
Benjamins, Joyce A.
[1
,2
,3
]
Nedelkoska, Liljana
[1
]
Touil, Hanane
[4
,5
,6
]
Stemmer, Paul M.
[7
]
Carruthers, Nicholas J.
[7
]
Jena, Bhanu P.
[8
]
Naik, Akshata R.
[8
]
Bar-Or, Amit
[4
,5
,6
]
Lisak, Robert P.
[1
,2
,3
]
机构:
[1] Wayne State Univ, Sch Med, Dept Neurol, Detroit, MI 48201 USA
[2] Wayne State Univ, Sch Med, Dept Biochem, Detroit, MI 48201 USA
[3] Wayne State Univ, Sch Med, Dept Immunol & Microbiol, Detroit, MI 48201 USA
[4] Univ Penn, Perelman Sch Med, Dept Neurol, Philadelphia, PA 19104 USA
[5] Univ Penn, Perelman Sch Med, Ctr Neuroinflammat & Expt Therapeut, Philadelphia, PA 19104 USA
[6] McGill Univ, Montreal Neurol Inst, Dept Neurol, Montreal, PQ, Canada
[7] Wayne State Univ, Inst Environm Hlth Sci, Detroit, MI USA
[8] Wayne State Univ, Sch Med, Dept Physiol, Detroit, MI 48201 USA
关键词:
MULTIPLE-SCLEROSIS;
CEREBROSPINAL-FLUID;
INFLAMMATION;
DEMYELINATION;
EXPRESSION;
ANTIBODIES;
APOPTOSIS;
PROFILES;
PROTEINS;
RELEASE;
D O I:
10.1212/NXI.0000000000000550
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
100204 [神经病学];
摘要:
Objective To identify whether factors toxic to oligodendrocytes (OLs), released by B cells from patients with MS, are found in extracellular microvesicles enriched in exosomes. Methods Conditioned medium (Sup) was obtained from cultures of blood B cells of patients with MS and normal controls (NCs). Exosome-enriched (Ex-En) fractions were prepared by solvent precipitation from Sup containing bovine serum and from serum-free Sup by ultracentrifugation (UC) or immunoprecipitation (IP) with antibodies to CD9. Ex-En fractions were diluted 1:4 with OL culture medium and screened for toxic effects on cultured rat OLs as measured by trypan blue uptake. Proteomic analysis was performed on Sup fractions. Results MS B cell-derived Ex-En fractions prepared from Sup by solvent extraction, UC, or IP induced OL death, whereas corresponding Ex-En fractions from NC showed little toxicity. Proteomic analysis of Sup demonstrated enrichment of proteins characteristic of exosomes from both NC and MS B-cell Sup. Ontology enrichment analysis suggested differences in the types and cargo of exosomes from MS Sup compared with NC, with proteins related to cell surface, extracellular plasma membrane, and gliogenesis enriched in MS. Conclusions Much of the in vitro toxicity of Sup from B cells of patients with relapsing-remitting MS is found in Ex-En fractions, as confirmed by 3 methods. Proteomic analysis of B-cell Sup indicates multiple differences between MS and NC.
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