ENAGenomicsMultiomicsAustralian Institute for Bioengineering and Nanotechnologyhttps://www.ebi.ac.uk/ena/browser/view/PRJNA274370Homo sapiensChronic inflammation leading to pro-inflammatory macrophage infiltration contributes to the pathogenesis of type 2 diabetes and subsequently the development of diabetic nephropathy. Mesenchymal stem cells (MSCs) possess unique immunomodulatory and cytoprotective properties making them an ideal candidate for therapeutic intervention We used microarrays to detail changes in the gene expression profile of monocytes isolated from type 2 diabetic patients with end-stage renal disease and non-diabetic control subjects following co-culture with MSCs. Overall design: Control blood samples were obtained from 4 donors from the Australian Red Cross Blood Service. Blood was also obtained from 5 diabetic patients with end-stage renal disease receiving haemodialysis at the Monash Medial Centre. CD14+ monocytes were isolated from blood using microbeads and co-cultured for 48 hours with and without human bone marrow-derived MSCs using an in vitro transwell system. An Affymetrix GeneChip Human Gene 2.0 ST array was used.xref:PubMed:26544198ENAbone marrow stromal cells, DmelCG1030, scr, SCR, data, BMSC, conditioned mesenchymal stem cell, DmScr, l(3)84Af, colony-forming unit-fibroblast, MYOR, Myor, MyoR, bHLHa22, marrow stromal cells, BG:DS07876.2, ABF1, CG1030, BHLHA22, ABF-1, MSC, Msc, Monocyte.Human, Modern., human being, Man (Taxonomy), Homo sapiens, man, Man, human, Modern ManfalseHomo sapiensExpression data from MSC-treated monocytes2025-09-242015-11-11PRJNA274370GSE65561960626544198