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. Author manuscript; available in PMC: 2011 Jun 16.
Published in final edited form as: Arthritis Rheum. 2009 Jun;60(6):1604–1614. doi: 10.1002/art.24574

Table 1.

Cytokine, chemokine, and growth factor levels in galectin 3–stimulated and unstimulated RA synovial and skin fibroblasts*

Analyte concentration, pg/ml

RA synovial fibroblasts
RA skin fibroblasts
Unstimulated Galectin 3–stimulated Unstimulated Galectin 3–stimulated
bFGF <10 <10 <10 <10
G-CSF
VEGF 10.1–50 50.1–100 <10
IFNγ
IFNα
IL-1β <10 <10 <10 <10
CCL4 <10 10.1–50 <10 <10
CXCL1 <10 10.1–50 <10
CXCL9 10.1–50 10.1–50 10.1–50 10.1–50
CXCL10 <10
MMP-9 <10 <10 <10 <10
MMP-13
*

Supernatants from rheumatoid arthritis (RA) synovial fibroblasts were cultured in medium alone (unstimulated) or with 10 μg/ml of galectin 3, and were assayed by multiplex enzyme-linked immunosorbent assay (ELISA) for cytokines and chemokines, and by ELISA for IL-6 (lower detection limit 15 pg/ml). Duplicate wells for each sample were analyzed. Values are those obtained after background levels were subtracted. bFGF = basic fibroblast growth factor; G-CSF = granulocyte colony-stimulating factor; – = undetectable or <1 pg/ml; VEGF = vascular endothelial growth factor; IFNγ = interferon-γ; MMP-9 = matrix metalloproteinase 9.