Skip to main content
. 2017 May 8;12(5):e0176523. doi: 10.1371/journal.pone.0176523

Table 5. The p values calculated using the Wilcoxon signed rank test for each gene in the three healthy donor cartilage discs in response to GDF5.

A Wildtype GDF5 B GDF5 variant
Gene Time point Gene Time point
Day 3 Day 7 Day 3 Day 7
ACAN 0.0078 (inc) 0.50 ACAN 0.023 (dec) 0.82
COL2A1 0.50 0.25 COL2A1 0.50 0.91
SOX9 0.69 0.027 (inc) SOX9 1.00 0.0039 (inc)
TIMP1 0.81 0.36 TIMP1 0.94 0.16
ADAMTS4 0.016 (inc) 0.91 ADAMTS4 0.13 0.019 (inc)
ADAMTS5 0.65 0.30 ADAMTS5 0.22 0.039 (inc)
MMP1 0.22 0.43 MMP1 0.94 0.74
MMP13 0.31 0.016 (inc) MMP13 0.0078 (dec) 0.055
BGLAP 0.81 0.94 BGLAP 0.58 1.00
COL1A1 0.012 (dec) 0.38 COL1A1 0.078 0.11
COL10A1 0.13 1.00 COL10A1 0.098 0.25
IHH 0.43 0.64 IHH 0.15 0.84
RUNX2 0.58 1.00 RUNX2 0.38 0.57
RUNX2 bn 0.69 1.00 RUNX2 bn 0.031 (inc) 0.30

Data derives from Tables 3 and 4. Comparisons were between untreated (control) and treatment with either exogenous wildtype GDF5 (A) or with GDF5 variant (B). P values <0.05 and arising from fold changes in the same direction for all three donors are highlighted in bold. RUNX2 bn, bone specific RUNX2 transcript. (inc), increased expression; (dec), decreased expression.