Growth Hormone Reprograms Macrophages toward an Anti-Inflammatory and Reparative Profile in an MAFB-Dependent Manner

被引:22
作者
Soler Palacios, Blanca [1 ]
Nieto, Concha [2 ]
Fajardo, Pilar [1 ]
Gonzalez de la Aleja, Arturo [2 ]
Andres, Nuria [1 ]
Dominguez-Soto, Angeles [2 ]
Lucas, Pilar [1 ]
Cuenda, Ana [1 ]
Miguel Rodriguez-Frade, Jose [1 ]
Martinez-A, Carlos [1 ]
Villares, Ricardo [1 ]
Corbi, Angel L. [2 ]
Mellado, Mario [1 ]
机构
[1] CSIC, Dept Inmunol & Oncol, Ctr Nacl Biotecnol, Madrid 28049, Spain
[2] CSIC, Dept Biol Mol & Celular, Ctr Invest Biol, Calle Raminor de Maeztu 9, Madrid 28040, Spain
关键词
GLYCOGEN-SYNTHASE KINASE-3; HUMAN T-CELLS; FACTOR-I; GH RECEPTOR; ACTIVIN-A; PHOSPHATIDYLINOSITOL; 3-KINASE; GENE-EXPRESSION; INSULIN; POLARIZATION; MUSCLE;
D O I
10.4049/jimmunol.1901330
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Growth hormone (GH), a pleiotropic hormone secreted by the pituitary gland, regulates immune and inflammatory responses. In this study, we show that GH regulates the phenotypic and functional plasticity of macrophages both in vitro and in vivo. Specifically, GH treatment of GM-CSF-primed monocyte-derived macrophages promotes a significant enrichment of anti-inflammatory genes and dampens the proinflammatory cytokine profile through PI3K-mediated downregulation of activin A and upregulation of MAFB, a critical transcription factor for anti-inflammatory polarization of human macrophages. These in vitro data correlate with improved remission of inflammation and mucosal repair during recovery in the acute dextran sodium sulfate-induced colitis model in GH-overexpressing mice. In this model, in addition to the GH-mediated effects on other immune cells, we observed that macrophages from inflamed gut acquire an anti-inflammatory/reparative profile. Overall, these data indicate that GH reprograms inflammatory macrophages to an anti-inflammatory phenotype and improves resolution during pathologic inflammatory responses.
引用
收藏
页码:776 / 788
页数:13
相关论文
共 78 条
[1]   GH activity and markers of inflammation: a crossover study in healthy volunteers treated with GH and a GH receptor antagonist [J].
Andreassen, Mikkel ;
Frystyk, Jan ;
Faber, Jens ;
Kristensen, Lars Ostergaard .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2012, 166 (05) :811-819
[2]   Activins A and B Regulate Fate-Determining Gene Expression in Islet Cell Lines and Islet Cells From Male Mice [J].
Andrzejewski, Danielle ;
Brown, Melissa L. ;
Ungerleider, Nathan ;
Burnside, Amy ;
Schneyer, Alan L. .
ENDOCRINOLOGY, 2015, 156 (07) :2440-2450
[3]   MURINE MACROPHAGES EXPRESS ABUNDANT INSULIN-LIKE GROWTH FACTOR-I CLASS-I EA AND EB TRANSCRIPTS [J].
ARKINS, S ;
REBEIZ, N ;
BIRAGYN, A ;
REESE, DL ;
KELLEY, KW .
ENDOCRINOLOGY, 1993, 133 (05) :2334-2343
[4]   The NLRP3 inflammasome is released as a particulate danger signal that amplifies the inflammatory response [J].
Baroja-Mazo, Alberto ;
Martin-Sanchez, Fatima ;
Gomez, Ana I. ;
Martinez, Carlos M. ;
Amores-Iniesta, Joaquin ;
Compan, Vincent ;
Barbera-Cremades, Maria ;
Yaguee, Jordi ;
Ruiz-Ortiz, Estibaliz ;
Anton, Jordi ;
Bujan, Segundo ;
Couillin, Isabelle ;
Brough, David ;
Arostegui, Juan I. ;
Pelegrin, Pablo .
NATURE IMMUNOLOGY, 2014, 15 (08) :738-+
[5]   Glycogen synthase kinase-3 (GSK3): Regulation, actions, and diseases [J].
Beurel, Eleonore ;
Grieco, Steven F. ;
Jope, Richard S. .
PHARMACOLOGY & THERAPEUTICS, 2015, 148 :114-131
[6]  
Bidlingmaier M, 1997, ACTA PAEDIATR, V86, P80
[7]   Rapid accumulation of Akt in mitochondria following phosphatidylinositol 3-kinase activation [J].
Bijur, GN ;
Jope, RS .
JOURNAL OF NEUROCHEMISTRY, 2003, 87 (06) :1427-1435
[8]   A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse [J].
Nolan, PM ;
Peters, J ;
Strivens, M ;
Rogers, D ;
Hagan, J ;
Spurr, N ;
Gray, IC ;
Vizor, L ;
Brooker, D ;
Whitehill, E ;
Washbourne, R ;
Hough, T ;
Greenaway, S ;
Hewitt, M ;
Liu, XH ;
McCormack, S ;
Pickford, K ;
Selley, R ;
Wells, C ;
Tymowska-Lalanne, Z ;
Roby, P ;
Glenister, P ;
Thornton, C ;
Thaung, C ;
Stevenson, JA ;
Arkell, R ;
Mburu, P ;
Hardisty, R ;
Kiernan, A ;
Erven, H ;
Steel, KP ;
Voegeling, S ;
Guenet, JL ;
Nickols, C ;
Sadri, R ;
Naase, M ;
Isaacs, A ;
Davies, K ;
Browne, M ;
Fisher, EMC ;
Martin, J ;
Rastan, S ;
Brown, SDM ;
Hunter, J .
NATURE GENETICS, 2000, 25 (04) :440-443
[9]   EFFECTS OF BOVINE GROWTH-HORMONE (BGH) TRANSGENE EXPRESSION OR BGH TREATMENT ON REPRODUCTIVE FUNCTIONS IN FEMALE MICE [J].
CECIM, M ;
KERR, J ;
BARTKE, A .
BIOLOGY OF REPRODUCTION, 1995, 52 (05) :1144-1148
[10]  
Chen YG, 2006, EXP BIOL MED, V231, P534