Transcriptional profiling of mouse bone marrow-derived macrophages (BMDMs) upon treatment with the S-palmitoylation inhibitor 2BP and/or myelin

ABSTRACT: The formation of inflammatory foamy macrophages hinders brain repair in multiple sclerosis. Therefore, the phenotype of the macrophages can determine the repair status of brain lesions. Here, we established the impact of the general S-palmitoylation inhibitor 2BP on the phenotype of bone marrow-derived macrophages (BMDMs) that were either treated with (Mye-BMDM) or without (BMDM) myelin after which .

INSTRUMENT(S): Illumina NovaSeq X

ORGANISM(S): Mus musculus

SUBMITTER: Jeroen Guns 

PROVIDER: E-MTAB-15390 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress