Macrophages: Master Regulators of Inflammation and Fibrosis

被引:1123
作者
Wynn, Thomas A. [1 ]
Barron, Luke [1 ]
机构
[1] NIAID, Immunopathogenesis Sect, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
关键词
Fibrosis; inflammation; collagen; wound healing; stellate cell; myofibroblasts; interleukin-13; transforming growth factor beta; tumor necrosis factor; interleukin-1; interleukin-17; arginase; Relm-alpha; chitinase; ALTERNATIVELY ACTIVATED MACROPHAGES; GROWTH-FACTOR-BETA; INDUCED PULMONARY-FIBROSIS; HEPATIC STELLATE CELLS; NITRIC-OXIDE SYNTHASE; CD4(+) T-CELLS; OSTEOPONTIN-DEFICIENT MICE; GENE-EXPRESSION PROFILES; ANTIGEN-PRESENTING CELLS; INNATE IMMUNE-RESPONSE;
D O I
10.1055/s-0030-1255354
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Macrophages are found in close proximity with collagen-producing myofibroblasts and indisputably play a key role in fibrosis. They produce profibrotic mediators that directly activate fibroblasts, including transforming growth factor-beta 1 and platelet-derived growth factor, and control extracellular matrix turnover by regulating the balance of various matrix metalloproteinases and tissue inhibitors of matrix metalloproteinases. Macrophages also regulate fibrogenesis by secreting chemokines that recruit fibroblasts and other inflammatory cells. With their potential to act in both a pro- and antifibrotic capacity, as well as their ability to regulate the activation of resident and recruited myofibroblasts, macrophages and the factors they express are integrated into all stages of the fibrotic process. These various, and sometimes opposing, functions may be performed by distinct macrophage subpopulations, the identification of which is a growing focus of fibrosis research. Although collagen-secreting myofibroblasts once were thought of as the master "producers" of fibrosis, this review will illustrate how macrophages function as the master "regulators" of fibrosis.
引用
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页码:245 / 257
页数:13
相关论文
共 176 条
[71]  
Keane MP, 1999, J IMMUNOL, V162, P5511
[72]   Transforming growth factor (TGF)-β1-producing regulatory T cells induce Smad-mediated interleukin 10 secretion that facilitates coordinated immunoregulatory activity and amelioration of TGF-β1-mediated fibrosis [J].
Kitani, A ;
Fuss, I ;
Nakamura, K ;
Kumaki, F ;
Usui, T ;
Strober, W .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (08) :1179-1188
[73]   Enhanced osteopontin expression in a murine model of allergen-induced airway remodelling [J].
Kohan, M. ;
Bader, R. ;
Puxeddu, I. ;
Levi-Schaffer, F. ;
Breuer, R. ;
Berkman, N. .
CLINICAL AND EXPERIMENTAL ALLERGY, 2007, 37 (10) :1444-1454
[74]   Transient expression of IL-1β induces acute lung injury and chronic repair leading to pulmonary fibrosis [J].
Kolb, M ;
Margetts, PJ ;
Anthony, DC ;
Pitossi, F ;
Gauldie, J .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (12) :1529-1536
[75]   Interleukin-13 induces tissue fibrosis by selectively stimulating and activating transforming growth factor β1 [J].
Lee, CG ;
Homer, R ;
Zhou, Z ;
Lanone, Z ;
Wang, XM ;
Koteliansky, V ;
Shipley, JM ;
Gotwals, P ;
Noble, P ;
Chen, QS ;
Senior, RM ;
Elias, JA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (06) :809-821
[76]   Role of breast regression protein 39 (BRP-39)/chitinase 3-like-1 in Th2 and IL-13-induced tissue responses and apoptosis [J].
Lee, Chun Geun ;
Hartl, Dominik ;
Lee, Gap Ryol ;
Koller, Barbara ;
Matsuura, Hiroshi ;
Da Silva, Carla A. ;
Sohn, Myung Hyun ;
Cohn, Lauren ;
Homer, Robert J. ;
Kozhich, Alexander A. ;
Humbles, Alison ;
Kearley, Jennifer ;
Coyle, Anthony ;
Chupp, Geoffrey ;
Reed, Jennifer ;
Flavell, Richard A. ;
Elias, Jack A. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2009, 206 (05) :1149-1166
[77]   CD14-positive hepatic monocytes/macrophages increase in hereditary hemochromatosis [J].
Leicester, KL ;
Olynyk, JK ;
Brunt, EM ;
Britton, RS ;
Bacon, BR .
LIVER INTERNATIONAL, 2004, 24 (05) :446-451
[78]   The plasminogen-activating system in hepatic stellate cells [J].
Leyland, H ;
Gentry, J ;
Arthur, MJP ;
Benyon, RC .
HEPATOLOGY, 1996, 24 (05) :1172-1178
[79]   Bone Marrow Ly6Chigh Monocytes Are Selectively Recruited to Injured Kidney and Differentiate into Functionally Distinct Populations [J].
Lin, Shuei Liong ;
Castano, Ana P. ;
Nowlin, Brian T. ;
Lupher, Mark L., Jr. ;
Duffield, Jeremy S. .
JOURNAL OF IMMUNOLOGY, 2009, 183 (10) :6733-6743
[80]   Notch1 Signaling in FIZZ1 Induction of Myofibroblast Differentiation [J].
Liu, Tianju ;
Hu, Biao ;
Choi, Yoon Young ;
Chung, MyoungJa ;
Ullenbruch, Matthew ;
Yu, Hongfeng ;
Lowe, John B. ;
Phan, Sem H. .
AMERICAN JOURNAL OF PATHOLOGY, 2009, 174 (05) :1745-1755