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Table 1 Effect of pharmacologic inhibitors on MSU phagocytosis by OBs

From: NLRP3 promotes autophagy of urate crystals phagocytized by human osteoblasts

 

Vacuole number (statistics)*

Control

13.1 ± 3.7 (a)

+ MSU

361 ± 27 (b)

Cytochalasin D + MSU

23.2 ± 10.7 (a)

Colchicine + MSU

321 ± 60 (b)

Control

14.5 ± 3.0 (a)

+ MSU

323 ± 32 (b)

Wortmannin + MSU

157 ± 31 (c)

LY4294002 + MSU

146 ± 27 (c)

Control

16.1 ± 3.2 (a)

+ MSU

281 ± 52 (b)

GF109203X + MSU

126 ± 10 (a)

Gö6976 + MSU

95 ± 10 (a)

SB203580 + MSU

612 ± 101 (c)

PD98069 + MSU

157 ± 39 (a)

Control

16.3 ± 3.2 (a)

+ MSU

193 ± 23 (b)

Piceatannol + MSU

82 ± 20 (a)

PP2 + MSU

231 ± 42 (b)

  1. Confluent OBs were preincubated 15 minutes with 1 μM cytochalasin D or 10 μM colchicine at 37°C and then stimulated with 0.5 mg MSU/106 cells for 24 hours. Confluent OBs were preincubated with PI3K inhibitors: wortmannin 50 nM or LY4294002 10 μM, with PKC inhibitors: GF109203X 5 μM or Gö6976 1 μM, with p38 or ERK1/2 inhibitors: SB203580 10 μM or PD98069 20 μM, or with a Syk inhibitor: piceatannol 20 μM and a Src inhibitor: PP2 10 μM, 15 minutes at 37°C and then stimulated with 0.5 mg MSU/106 cells for 24 hours. Cells were analyzed with microscopy (×200 magnification), and results expressed as cumulative data means of values ± SEM of five pictures for each donor. Statistical analysis was performed on vacuole counts by using the repeated measures ANOVA followed by Tukey multiple-comparison test (n = 4 different donors). *Means without a common letter differ: P < 0.05.