Title : Hydroxycarboxylic acid receptor 2 mediates dimethyl fumarate's protective effect in EAE.

Pub. Date : 2014 May

PMID : 24691444






12 Functional Relationships(s)
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1 Hydroxycarboxylic acid receptor 2 mediates dimethyl fumarate"s protective effect in EAE. Dimethyl Fumarate hydroxycarboxylic acid receptor 2 Mus musculus
2 DMF and, more so, its active metabolite, monomethyl fumarate, are known agonists of the hydroxycarboxylic acid receptor 2 (HCA2), a G protein-coupled membrane receptor. Dimethyl Fumarate hydroxycarboxylic acid receptor 2 Mus musculus
3 DMF and, more so, its active metabolite, monomethyl fumarate, are known agonists of the hydroxycarboxylic acid receptor 2 (HCA2), a G protein-coupled membrane receptor. Dimethyl Fumarate hydroxycarboxylic acid receptor 2 Mus musculus
4 Here, we evaluated the contribution of HCA2 in mediating the protective effect afforded by DMF in EAE, a mouse model of MS. DMF treatment reduced neurological deficit, immune cell infiltration, and demyelination of the spinal cords in wild-type mice, but not in Hca2-/- mice, indicating that HCA2 is required for the therapeutic effect of DMF. Dimethyl Fumarate hydroxycarboxylic acid receptor 2 Mus musculus
5 Here, we evaluated the contribution of HCA2 in mediating the protective effect afforded by DMF in EAE, a mouse model of MS. DMF treatment reduced neurological deficit, immune cell infiltration, and demyelination of the spinal cords in wild-type mice, but not in Hca2-/- mice, indicating that HCA2 is required for the therapeutic effect of DMF. Dimethyl Fumarate hydroxycarboxylic acid receptor 2 Mus musculus
6 Here, we evaluated the contribution of HCA2 in mediating the protective effect afforded by DMF in EAE, a mouse model of MS. DMF treatment reduced neurological deficit, immune cell infiltration, and demyelination of the spinal cords in wild-type mice, but not in Hca2-/- mice, indicating that HCA2 is required for the therapeutic effect of DMF. Dimethyl Fumarate hydroxycarboxylic acid receptor 2 Mus musculus
7 Here, we evaluated the contribution of HCA2 in mediating the protective effect afforded by DMF in EAE, a mouse model of MS. DMF treatment reduced neurological deficit, immune cell infiltration, and demyelination of the spinal cords in wild-type mice, but not in Hca2-/- mice, indicating that HCA2 is required for the therapeutic effect of DMF. Dimethyl Fumarate hydroxycarboxylic acid receptor 2 Mus musculus
8 Here, we evaluated the contribution of HCA2 in mediating the protective effect afforded by DMF in EAE, a mouse model of MS. DMF treatment reduced neurological deficit, immune cell infiltration, and demyelination of the spinal cords in wild-type mice, but not in Hca2-/- mice, indicating that HCA2 is required for the therapeutic effect of DMF. Dimethyl Fumarate hydroxycarboxylic acid receptor 2 Mus musculus
9 Here, we evaluated the contribution of HCA2 in mediating the protective effect afforded by DMF in EAE, a mouse model of MS. DMF treatment reduced neurological deficit, immune cell infiltration, and demyelination of the spinal cords in wild-type mice, but not in Hca2-/- mice, indicating that HCA2 is required for the therapeutic effect of DMF. Dimethyl Fumarate hydroxycarboxylic acid receptor 2 Mus musculus
10 Here, we evaluated the contribution of HCA2 in mediating the protective effect afforded by DMF in EAE, a mouse model of MS. DMF treatment reduced neurological deficit, immune cell infiltration, and demyelination of the spinal cords in wild-type mice, but not in Hca2-/- mice, indicating that HCA2 is required for the therapeutic effect of DMF. Dimethyl Fumarate hydroxycarboxylic acid receptor 2 Mus musculus
11 In particular, DMF decreased the number of infiltrating neutrophils in a HCA2-dependent manner, likely by interfering with neutrophil adhesion to endothelial cells and chemotaxis. Dimethyl Fumarate hydroxycarboxylic acid receptor 2 Mus musculus
12 Together, our data indicate that HCA2 mediates the therapeutic effects of DMF in EAE. Dimethyl Fumarate hydroxycarboxylic acid receptor 2 Mus musculus