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Table 3 Chemokine and chemokine receptor expression data analysis

From: Chemokine receptors in the rheumatoid synovium: upregulation of CXCR5

Gene

RA

Non-RA

Regulation (ratio RA/non-RA)

Receptors

Array column 3 (Fig. 1, C3)

   CCR1

0.050

0.023

Up (2.2 ± 0.2)

   CCR2a

0.031

0.012 ○●

Up (2.7 ± 0.2)

   CCR2b

0.000 ○

0.000 ○

Not visible (NA)

   CCR3

0.000 ○

0.000 ○

Not visible (NA)

   CCR4

0.003 ○

0.000 ○

Not visible (NA)

   CCR5

0.042

0.000 ○●

Up (NA)

   CCR6

0.001 ○

0.000 ○

Not visible (NA)

   CCR7

0.022 ○●

0.011 ○

Not visible (2.5 ± 0.9)

   CCR9

0.001 ○●

0.000 ○

Not visible (NA)

   CX3CR1

0.028 ○●

0.019 ○●

Not visible (1.5 ± 0.1)

   CXCR1

0.036 ○●

0.008 ○●

Not visible (9.6 ± 5.6)

   CXCR2

0.651

0.000 ○●

Up (NA)

   CXCR4

0.190

0.055

Up (3.5 ± 0.1)

   CXCR5

1.328

0.059

Up (22.6 ± 0.7)

   CXCR6 (STRL33)

0.016

0.025

Not visible (0.7 ± 0.0)

   Bob

0.034

0.000 ○

Up (NA)

Chemokines

Array column 1 (Fig. 1, C1)

   CCL21 (6Ckine)

0.030

0.019 ○

Up (1.6 ± 0.1)

   CXCL13 (BLC/BCA-1)

0.052

0.020 ○

Up (2.8 ± 0.4)

   CXCL10 (IP-10)

0.031

0.019 ○●

Up (1.6 ± 0.1)

   CXCL5 (ENA-78)

0.050

0.015 ○●

Up (3.5 ± 0.3)

   CCL11 (eotaxin)

0.050

0.052

Not visible (1.0 ± 0.0)

   CCL24 (eotaxin-2)

0.032

0.013 ○

Up (2.5 ± 0.3)

   CX3CL1 (fractalkine)

0.030 ○●

0.012 ○

Not visible (2.5 ± 0.2)

   CXCL1 (GRO-α)

0.090

0.057

Up (1.6 ± 0.0)

   CXCL2 (GRO-β)

0.151

0.101

Up (1.5 ± 0.0)

   CXCL3 (GRO-γ)

0.101

0.055

Up (1.8 ± 0.0)

   CCL14 (HCC-1)

0.202

0.296

Down (0.7 ± 0.0)

   CCL16 (HCC-4)

0.006 ○●

0.000 ○

Not visible (NA)

   CCL1 (I-309)

0.007 ○●

0.000 ○

Not visible (NA)

   CXCL8 (IL-8)

0.086

0.026

Up (3.3 ± 0.2)

   CXCL7 (LDGF)

0.005 ○

0.000 ○

Not visible (NA)

   CCL15 (MIP-1δ)

0.009 ○●

0.008 ○

Not visible (11 ± 13)

   XCL1 (lymphotactin)

0.048

0.031

Up (1.6 ± 0.0)

   CCL2 (MCP-1)

0.482

0.545

Not visible (0.9 ± 0.0)

   CCL8 (MCP-2)

0.053

0.062

Not visible(0.9 ± 0.0)

   CCL7 (MCP-3)

0.066

0.047

Up (1.4 ± 0.1)

   CCL13 (MCP-4)

0.000 ○

0.002 ○

Not visible (0.0)

   CCL22 (MDC)

0.000 ○●

0.008 ○

Not visible (0.0)

Array column 2 (Fig. 1, C2)

   Midkine

0.299

0.155

Up (1.9 ± 0.0)

   CXCL9 (MIG)

0.166

0.047

Up (3.6 ± 0.1)

   CCL3 (MIP-1α)

0.040

0.042

Not visible (1.0 ± 0.0)

   CCL4 (MIP-1β)

0.023

0.018 ○●

Up (1.3 ± 0.2)

   CCL20 (MIP-3α)

0.000 ○

0.013 ○

Not visible(0.0)

   CCL19 (MIP-3β)

0.023

0.042

Not visible (0.6 ± 0.0)

   CCL23 (MPIF-1)

0.039

0.042

Up (0.9 ± 0.0)

   CCL18 (PARC)

0.146

0.033

Up (4.5 ± 0.4)

   CCL5 (RANTES)

0.037

0.031

Up (1.2 ± 0.1)

   CXCL12 (SDF-1)

0.409

0.573

Down (0.7 ± 0.0)

   CCL17 (TARC)

0.000 ○

0.000 ○

Not visible (NA)

   CCL25 (TECK)

0.000 ○

0.000 ○

Not visible (NA)

  1. Following hybridization to labelled mRNA extracted from rheumatoid arthritis (RA) and non-RA synovia, a pair of array membranes was autoradiographed for varying lengths of time. The autoradiograms were scanned and analysed with the ArrayVision software (version 6.0; Imaging Research Inc., Haverhill, UK). For each RA/non-RA pair the housekeeping genes on the membranes showed very similar intensities, were not saturated and were used to normalize the data. The analysis measured the 'volume' of each spot (i.e. the density value of each spot multiplied by its area). The background was measured using the 'corners between spots' protocol of the software and was deducted from the 'volumes'. The ratio of RA synovia versus non-RA synovia was also calculated for each spot. The analysis was repeated eight times for each pair of autoradiograms, providing 16 values for each gene (each gene is spotted in duplicate) on each pair. Figures in the columns RA, non-RA and ratio RA/non-RA represent the average of 16 values. For each average ratio the 95% confidence level was calculated, and the results presented are those from the autoradiogram pair giving the smallest variation. ○, spot was not visible by eye on the corresponding autoradiogram; ●, spot was visible after prolonged exposure. The mRNA regulation of RA versus non-RA as observed by eye at the time point used for quantification is indicated by not visible, up or down. NA, ratio could not be calculated due to the presence of zero values. The recent systematic nomenclature of chemokines is used, with the former names in parentheses. The order of the genes presented is the same as that appearing on the microarray in Fig. 1.
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Arthritis Research & Therapy

ISSN: 1478-6362

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