| Literature DB >> 34541112 |
Yuki Tanaka1, Yasunobu Arima1, Kotaro Higuchi1, Takuto Ohki1, Mohamed Elfeky1, Mitsutoshi Ota1, Daisuke Kamimura1, Masaaki Murakami1.
Abstract
Experimental autoimmune encephalomyelitis (EAE) is an animal model of multiple sclerosis (MS), which is a chronic inflammatory disease of the central nervous system (CNS). It is characterized by focal demyelination and inflammatory responses mediated by myelin-specific autoreactive CD4+ T cells. Using a passive transfer model of EAE in mice, we have demonstrated that regional specific neural signals by sensory-sympathetic communications create gateways for immune cells at specific blood vessels of the CNS, a phenomenon known as the gateway reflex ( Arima et al., 2012 ; Tracey, 2012; Arima et al., 2013 ; Sabharwal et al., 2014 ; Arima et al., 2015b ). Here we describe protocols for passive transfer model of EAE using freshly isolated (MOG)-specific CD4+ T cells or periodically restimulated MOG-specific CD4+ T cell lines, which are suitable for tracking pathogenic CD4+ T cells in vivo, particularly in the CNS ( Ogura et al., 2008 ; Arima et al., 2012 and 2015b).Entities:
Keywords: Pathogenic CD4+ T cells ; Experimental autoimmune encephalomyelitis; Gateway reflex; Myelin oligodendrocyte glycoprotein; Passive transfer
Year: 2017 PMID: 34541112 PMCID: PMC8413655 DOI: 10.21769/BioProtoc.2370
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325