Cardiotrophin-1 is an anti-inflammatory cytokine and promotes IL-4-induced M2 macrophage polarization

被引:12
作者
Carneros, David [1 ]
Santamaria, Eva M. [2 ,4 ]
Larequi, Eduardo [2 ]
Miguel Velez-Ortiz, Jose [1 ]
Reboredo, Mercedes [2 ,4 ]
Mancheno, Uxua [3 ,6 ]
Jesus Perugorria, Maria [4 ,7 ]
Navas, Placido [5 ,8 ]
Romero-Gomez, Manuel [1 ,4 ]
Prieto, Jesus [2 ,4 ]
Hervas-Stubbs, Sandra [3 ,6 ]
Bustos, Matilde [1 ]
机构
[1] Univ Seville, Virgen del Rocio Univ Hosp, CSIC, Inst Biomed Seville IBiS, Avda Manuel Siurot S-N, Seville 41013, Spain
[2] Univ Navarra, Ctr Appl Med Res CIMA, Div Hepatol, Pamplona, Spain
[3] Univ Navarra, Ctr Appl Med Res CIMA, Div Immunol & Immunotherapy, Pamplona, Spain
[4] Inst Salud Carlos III, CIBEREHD, Madrid, Spain
[5] Inst Salud Carlos III, CIBERER, Madrid, Spain
[6] Inst Invest Sanitaria Navarra IdiSNA, Pamplona, Spain
[7] Univ Basque Country, Donostia Univ Hosp, Biodonostia Hlth Res Inst, UPV EHU, San Sebastian, Spain
[8] Univ Pablo Olavide, CSIC, CABD, Seville, Spain
关键词
interleukin-6; gp130; M1; IL-6; STAT3; ALTERNATIVE ACTIVATION; ONCOSTATIN M; INTERLEUKIN-6; RECEPTOR; INJURY; IL-6; EXPRESSION; MICE; ENDOTOXEMIA; MECHANISMS;
D O I
10.1096/fj.201801563R
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Macrophages play a central role in tissue remodeling, repair, and resolution of inflammation. Macrophage polarization to M1 or M2 activation status may determine the progression or resolution of the inflammatory response. We have previously reported that cardiotrophin-1 (CT-1) displays both cytoprotective and metabolic activities. The role of CT-1 in inflammation remains poorly understood. Here, we employed recombinant CT-1 (rCT-1) and used CT-1-null mice and myeloid-specific CT-1 transgenic mice to investigate whether CT-1 might play a role in the modulation of the inflammatory response. We observed that CT-1 deficiency was associated with enhanced release of inflammatory mediators and with stronger activation of NF-kappa B in response to LPS, whereas the inflammatory response was attenuated in CT-1 transgenic mice or by administering rCT-1 to wild-type animals prior to LPS challenge. We found that CT-1 promoted IL-6 expression only by nonhematopoietic cells, whereas LPS up-regulated IL-6 expression in both hematopoietic and nonhematopoietic cells. Notably, rCT-1 inhibited LPS-mediated soluble IL-6R induction. Using IL-6(-/-) mice, we showed that rCT-1 inhibited LPS-induced TNF-alpha and IFN-gamma response in an IL-6-independent manner. Importantly, we demonstrated that CT-1 primes macrophages for IL-4-dependent M2 polarization by inducing IL-4 receptor expression. Mechanistic analyses showed that the signal transducer and activator of transcription 3-suppressor of cytokine signaling 3 axis mediates this effect. Our findings support the notion that CT-1 is a critical regulator of inflammation and suggest that rCT-1 could be a molecule with potential therapeutic application in inflammatory conditions.-Carneros, D., Santamaria, E. M., Larequi, E., Velez-Ortiz, J. M., Reboredo, M., Mancheno, U., Perugorria, M. J., Navas, P., Romero-Gomez, M., Prieto, J., Hervas-Stubbs, S., Bustos, M. Cardiotrophin-1 is an anti-inflammatory cytokine and promotes IL-4-induced M2 macrophage polarization.
引用
收藏
页码:7578 / 7587
页数:10
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