| Literature DB >> 26464215 |
Ji-Eun Seo1,2,3, Mahbub Hasan1,2,3, Joon-Seung Han1,2, Nak-Kyoon Kim4, Ji Eun Lee5, Kang Mi Lee2, Ju-Hyung Park2, Ho Jun Kim2, Junghyun Son2, Jaeick Lee2, Oh-Seung Kwon6,7,8.
Abstract
Experimental autoimmune encephalomyelitis (EAE) is commonly induced with myelin oligodendrocyte glycoprotein (MOG)35-55; occasionally, EAE is not well induced despite MOG35-55 immunization. To confirm that EAE induction varies with difference in MOG35-55 properties, we compared three MOG35-55 from different commercial sources, which are MOG-A, MOG-B, and MOG-C. The peptides induced EAE disease with 100, 40, and 20 % incidence, respectively. Compared with others, MOG-A showed higher peptide purity (99.2 %) and content (92.2 %) and presented a sheet shape with additional sodium and chloride chemical elements. In MOG-A-treated group, MMP-9 activity and IL-6 levels were considerably higher than the other groups in CNS tissues, and significantly increased VCAM-1, IFN-γ, and decreased IL-4 were also shown compared to MOG-B- and/or MOG-C-treated group. In conclusion, the immunological and toxicological changes by the difference in MOG35-55 properties modulate EAE induction, and MOG35-55 which affects MMP-9 activity and IL-6 levels may be the most effective EAE-inducing antigen. This study can be potentially applied by researchers using MOG35-55 peptide and manufacturers for MOG35-55 synthesis.Entities:
Keywords: EAE; IL-6; Induction; MMP-9; MOG35-55; Property
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Year: 2015 PMID: 26464215 DOI: 10.1007/s11064-015-1732-9
Source DB: PubMed Journal: Neurochem Res ISSN: 0364-3190 Impact factor: 3.996