The results of the present in vitro study demonstrate that cultured SSc fibrocytes show a high pro-fibrotic activity compared to HS fibrocytes, as evidenced by their increased gene and protein expression of fibroblast/myofibroblast phenotype markers (S100A4 and αSMA), and ECM macromolecules (COL1 and FN), confirming that fibrocytes may serve as an important source of fibroblasts and myofibroblasts in SSc [17]. The gene discussed is ACTA1; the disease is systemic sclerosis.