In vivo gene expression revealed by cDNA arrays: the pattern in relapsing-remitting multiple sclerosis patients compared with normal subjects

Objectives: To use DNA arrays to identify differences in gene expression as sociated with relapsing-remitting (RR) MS. Methods: Total RNA was isolated from monocyte depleted peripheral blood mon onuclear cells of 15 RR MS patients and 15 age- and sex-matched controls. T he RNA was reverse transcribed to radiolabeled cDNA and the resultant cDNA was used to probe a DNA array containing over 4000 named human genes. The b inding of radiolabeled cDNA to the probes on the array was measured by phos phorimager. Results: Of more than 4000 genes tested, only 34 were significantly differe nt in RR-MS patients from controls. Of these, 25 were significantly increas ed and 9 significantly decreased in the RR MS patients. Twelve of these gen es have inflammatory and/or immunological functions that could be relevant to the MS disease process. The potentially relevant genes that were elevate d (15% to 28%) were P protein, LCK, cAMP responsive element modulator, IL-7 receptor, matrix metalloproteinase-19, M130 antigen, and peptidyl-prolyl i somerase. Those that were significantly decreased (15% to 35%) were SAS tra nsmembrane 4 superfamily protein. STRL22 (C-C chemokine receptor 6), AFX pr otein, DNA fragmentation factor-45 and immunoglobulin gamma 3 (Gm marker). Conclusions: The RR-MS disease effect was relatively restricted and most of the mRNAs tested were not different from the normal controls. However, the re were significant differences identified in the expression of a subset of mRNAs. including 13 with inflammatory/immune functions that could be relev ant to MS. The systematic use of DNA arrays can provide insight into the dy namic cellular pathways involved in MS pathogenesis and its phenotypic hete rogeneity. (C) 2001 Elsevier Science B.V. All rights reserved.