Figure 7.
Platelet-specific deletion of SHARPIN reduces neutrophil recruitment in a peritonitis model of sterile inflammation. (A) SHARPINfl/fl GPIbα-Cre− and SHARPINfl/fl GPIbα-Cre+ mice were injected with thioglycollate medium or saline and euthanized at 4 or 24 hours, and peritoneal lavage fluid was harvested. The number of neutrophils was determined as described in Methods (n = 5; **P < .01). (B) Western blot of lysate from SHARPINfl/GPIbα-Cre− or SHARPINfl/fl GPIbα-Cre+ mouse platelets or from harvested peritoneal lavage fluid, subjected to SDS-PAGE and blotted for SHARPIN. β-actin re-probes were used as a loading control. The blots are representative of results obtained with lysate from 3 mice each.

Platelet-specific deletion of SHARPIN reduces neutrophil recruitment in a peritonitis model of sterile inflammation. (A) SHARPINfl/fl GPIbα-Cre and SHARPINfl/fl GPIbα-Cre+ mice were injected with thioglycollate medium or saline and euthanized at 4 or 24 hours, and peritoneal lavage fluid was harvested. The number of neutrophils was determined as described in Methods (n = 5; **P < .01). (B) Western blot of lysate from SHARPINfl/GPIbα-Cre or SHARPINfl/fl GPIbα-Cre+ mouse platelets or from harvested peritoneal lavage fluid, subjected to SDS-PAGE and blotted for SHARPIN. β-actin re-probes were used as a loading control. The blots are representative of results obtained with lysate from 3 mice each.

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