Intestinal macrophages: well educated exceptions from the rule

被引:161
作者
Zigmond, Ehud [1 ,2 ]
Jung, Steffen [1 ]
机构
[1] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[2] Tel Aviv Univ, Tel Aviv Sourasky Med Ctr, Gastroenterol & Hepatol Inst, IL-69978 Tel Aviv, Israel
关键词
intestine; macrophages; monocytes; inflammatory bowel disorder; INFLAMMATORY-BOWEL-DISEASE; CD103(+) DENDRITIC CELLS; REGULATORY T-CELLS; LAMINA-PROPRIA; COSTIMULATORY MOLECULES; MUCOSAL MACROPHAGES; ULCERATIVE-COLITIS; IMMUNE-RESPONSES; EXPRESSION; GUT;
D O I
10.1016/j.it.2013.02.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Macrophages are the most abundant mononuclear phagocytes in the healthy intestinal lamina propria and have emerged as crucial sentinels for the maintenance of tissue homeostasis. Matching the dynamic mucosal landscape, CX3C chemokine receptor (CX3CR)1-expressing macrophages are relatively short lived, and as opposed to most other tissue macrophages, are continuously replaced from blood monocytes that acquire in the healthy tissue context a robust noninflammatory gene expression signature. By contrast, during gut inflammation, monocytes differentiate in the gut into proinflammatory effector cells, as well as migratory antigen-presenting cells. Manipulation of monocyte fates in the intestine might hold promise for the disease management of inflammatory bowel disorders.
引用
收藏
页码:162 / 168
页数:7
相关论文
共 91 条
[1]
Infiltrating monocytes trigger EAE progression, but do not contribute to the resident microglia pool [J].
Ajami, Bahareh ;
Bennett, Jami L. ;
Krieger, Charles ;
McNagny, Kelly M. ;
Rossi, Fabio M. V. .
NATURE NEUROSCIENCE, 2011, 14 (09) :1142-U263
[2]
Epithelial-cell recognition of commensal bacteria and maintenance of immune homeostasis in the gut [J].
Artis, David .
NATURE REVIEWS IMMUNOLOGY, 2008, 8 (06) :411-420
[3]
ATP drives lamina propria TH17 cell differentiation [J].
Atarashi, Koji ;
Nishimura, Junichi ;
Shima, Tatsuichiro ;
Umesaki, Yoshinori ;
Yamamoto, Masahiro ;
Onoue, Masaharu ;
Yagita, Hideo ;
Ishii, Naoto ;
Evans, Richard ;
Honda, Kenya ;
Takeda, Kiyoshi .
NATURE, 2008, 455 (7214) :808-U10
[4]
Induction of Colonic Regulatory T Cells by Indigenous Clostridium Species [J].
Atarashi, Koji ;
Tanoue, Takeshi ;
Shima, Tatsuichiro ;
Imaoka, Akemi ;
Kuwahara, Tomomi ;
Momose, Yoshika ;
Cheng, Genhong ;
Yamasaki, Sho ;
Saito, Takashi ;
Ohba, Yusuke ;
Taniguchi, Tadatsugu ;
Takeda, Kiyoshi ;
Hori, Shohei ;
Ivanov, Ivaylo I. ;
Umesaki, Yoshinori ;
Itoh, Kikuji ;
Honda, Kenya .
SCIENCE, 2011, 331 (6015) :337-341
[5]
Intra-bone marrow-bone marrow transplantation facilitates hemopoietic recovery including dendritic cells [J].
Baba, S ;
Inaba, M ;
Iwai, H ;
Taira, M ;
Takada, K ;
Hisha, H ;
Yamashita, T ;
Ikehara, S .
IMMUNOBIOLOGY, 2005, 210 (01) :33-42
[6]
Bain CC, 2012, MUCOSAL IMMUNOL
[7]
Berg Rodney D., 1995, Trends in Microbiology, V3, P149, DOI 10.1016/S0966-842X(00)88906-4
[8]
Origin of the Lamina Propria Dendritic Cell Network [J].
Bogunovic, Milena ;
Ginhoux, Florent ;
Helft, Julie ;
Shang, Limin ;
Hashimoto, Daigo ;
Greter, Melanie ;
Liu, Kang ;
Jakubzick, Claudia ;
Ingersoll, Molly A. ;
Leboeuf, Marylene ;
Stanley, E. Richard ;
Nussenzweig, Michel ;
Lira, Sergio A. ;
Randolph, Gwendalyn J. ;
Merad, Miriam .
IMMUNITY, 2009, 31 (03) :513-525
[9]
The proportion of CD40+ mucosal macrophages is increased in inflammatory bowel disease whereas CD40 ligand (CD154)+ T cells are relatively decreased, suggesting differential modulation of these costimulatory molecules in human gut lamina propria [J].
Carlsen, Hege S. ;
Yamanaka, Takeshi ;
Scott, Helge ;
Rugtveit, Jarle ;
Brandtzaeg, Per .
INFLAMMATORY BOWEL DISEASES, 2006, 12 (11) :1013-1024
[10]
Intestinal CD103- dendritic cells migrate in lymph and prime effector T cells [J].
Cerovic, V. ;
Houston, S. A. ;
Scott, C. L. ;
Aumeunier, A. ;
Yrlid, U. ;
Mowat, A. M. ;
Milling, S. W. F. .
MUCOSAL IMMUNOLOGY, 2013, 6 (01) :104-113