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Glucocorticoid receptor dimerization induces MKP1 to protect against TNF-induced inflammation
Sofie Vandevyver, … , Jan Tuckermann, Claude Libert
Sofie Vandevyver, … , Jan Tuckermann, Claude Libert
Published May 15, 2012
Citation Information: J Clin Invest. 2012;122(6):2130-2140. https://doi.org/10.1172/JCI60006.
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Research Article Immunology

Glucocorticoid receptor dimerization induces MKP1 to protect against TNF-induced inflammation

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Abstract

Glucocorticoids acting through the glucocorticoid receptor (GR) inhibit TNF-induced lethal inflammation. Here, we demonstrate that GR dimerization plays a role in reducing TNF sensitivity. In mutant mice unable to dimerize GR, we found that TNF failed to induce MAPK phosphatase 1 (MKP1). We assessed TNF sensitivity in Mkp1–/– mice and found increased inflammatory gene induction in livers, increased circulating cytokines, cell death in intestinal epithelium, severe intestinal inflammation, hypothermia, and death. Mkp1–/– mice had increased levels of phosphorylated JNK, which promotes apoptosis, in liver tissue. We further examined JNK-deficient mice for their response to TNF. Although Jnk1–/– mice showed no change in sensitivity to TNF, Jnk2–/– mice were significantly protected against TNF, identifying JNK2 as an essential player in inflammation induced by TNF. Furthermore, we found that loss of Jnk2 partially rescued the increased sensitivity of Mkp1–/– and mutant GR mice to TNF. Our data show that GR dimerization inhibits JNK2 through MKP1 and protects from TNF-induced apoptosis and lethal inflammation.

Authors

Sofie Vandevyver, Lien Dejager, Tom Van Bogaert, Anna Kleyman, Yusen Liu, Jan Tuckermann, Claude Libert

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Figure 2

Mkp1–/– mice are hypersensitive to TNF-induced lethality.

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Mkp1–/– mice are hypersensitive to TNF-induced lethality.
 
(A and B) S...
(A and B) Survival (A) and body temperature (B) of Mkp1+/+ (n = 12) and Mkp1–/– (n = 22) mice after injection of 5 μg TNF. *P < 0.05, ***P < 0.001, Mkp1–/– vs. Mkp1+/+. (C) Serum IL-6 levels and liver Il6 mRNA levels 0, 1, and 6 hours after 5 μg TNF (n = 5 per group). (D and E) Mice were injected i.p. with 5 μg TNF, and 0, 1, and 6 hours later, they were euthanized, and livers (D) and IECs (E) were isolated for qPCR analysis of Ccl5, Timp1 and Nos2 levels (n = 5 per group). (F) Standard H&E and active caspase 3 staining of ileum samples (n = 5 per group). Representative images are shown. The ileum was sampled 0 and 1 hour after injection of 5 μg TNF. The micrograph at the 0-hour time point is representative of both Mkp1+/+ and Mkp1–/– mice. Scale bars: 100 μm. Original magnification, ×40. (C–F) *P < 0.05, **P < 0.01, ***P < 0.001 vs. 0 hours or as indicated by brackets. (G and H) Survival of Mkp1+/+ (G) and Mkp1–/– (H) mice pretreated with 10 mg/kg DEX (squares; n = 8 per group) or solvent (circles; n = 8 [Mkp1+/+]; 7 [Mkp1–/–]) and injected with 15 μg (G) or 7.5 μg (H) TNF. **P < 0.01, DEX vs. solvent. (A–H) Black bars and symbols, Mkp1+/+; white bars and symbols, Mkp1–/–.

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