Dampened ERK signaling in hematopoietic progenitor cells in rheumatoid arthritis

In rheumatoid arthritis (RA), hematopoietic progenitor cells (HPC) have age-inappropriate telomeric shortening suggesting premature senescence and possible restriction of proliferative capacity. In response to hematopoietic growth factors RA-derived CD34+ HPC expanded significantly less than age-matched controls. Cell surface receptors for stem cell factor (SCF), Flt 3-Ligand, IL-3 and IL-6 were intact in RA HPC but the cells had lower transcript levels of cell cycle genes, compatible with insufficient signal strength in the ERK pathway. Cytokine-induced phosphorylation of ERK1/2 was diminished in RA HPC whereas phosphorylated STAT3 and STAT5 molecules accumulated to a similar extent as in controls. Confocal microscopy demonstrated that the membrane-proximal colocalization of K-Ras and B-Raf was less efficient in RA-derived CD34+ cells. Thus, hyporesponsiveness of RA HPC to growth factors results from dampening of the ERK signaling pathways; with a defect localized in the very early steps of the ERK signaling cascade.

► Hypo-proliferation of hematopoietic progenitor cells (HPC) in rheumatoid arthritis.
► Reduced c-myc expression in RA progenitor cells.
► Intact phosphorylation of STAT3 and STAT5 in RA HPC.
► Impaired activation of the ERK signaling pathway in RA HPC.
► Insufficient co-localization of K-Ras and B-Raf in proximal ERK signaling.