Tissue stroma as a regulator of leukocyte recruitment in inflammation

被引:62
作者
McGettrick, Helen M. [1 ,2 ]
Butler, Lynn M. [3 ]
Buckley, Chris D. [2 ]
Rainger, G. Ed [1 ]
Nash, Gerard B. [1 ]
机构
[1] Univ Birmingham, Sch Clin & Expt Med, Birmingham B15 2TT, W Midlands, England
[2] Univ Birmingham, Sch Immun & Infect, Birmingham B15 2TT, W Midlands, England
[3] Karolinska Inst, Ctr Mol Med, Stockholm, Sweden
关键词
endothelial cells; adhesion; migration; stroma; SMOOTH-MUSCLE-CELLS; TUMOR-NECROSIS-FACTOR; BLOOD-BRAIN-BARRIER; NEUTROPHIL TRANSENDOTHELIAL MIGRATION; FIBROBLAST-LIKE SYNOVIOCYTES; HUMAN POLYMORPHONUCLEAR LEUKOCYTES; PERIVASCULAR BASEMENT-MEMBRANE; VASCULAR ENDOTHELIAL-CELLS; TRANSMIGRATION IN-VIVO; CD4(+) T-CELLS;
D O I
10.1189/jlb.0911458
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The stromal milieu (cellular and matrix components) helps establish tissue "address-codes" that direct leukocyte behavior in inflamed tissue. Coordinated interactions among the stroma, leukocytes, and ECs dictate which leukocytes are recruited, whether they are retained within the inflamed site, and how long they survive. Herein, we discuss how the stromal milieu influences the leukocyte recruitment cascade. Moreover, we explore how corruption of the stromal phenotype in chronic inflammatory diseases contributes to undesired, continuous recruitment of leukocytes. Emerging complex, multicellular, multilayered (co-) culture models are now addressing the molecular circuitry involved in regulating stromal organization during inflammation. Understanding context-specific changes in pro-or anti-inflammatory agents derived from the stroma, such as IL-6 (and its cofactors), is important for the generation of therapeutic strategies that restore the balance between recruitment and clearance of the inflammatory infiltrate in chronic disease. J. Leukoc. Biol. 91: 385-400; 2012.
引用
收藏
页码:385 / 400
页数:16
相关论文
共 171 条
[1]   Prostaglandin D2 Regulates CD4+ Memory T Cell Trafficking across Blood Vascular Endothelium and Primes These Cells for Clearance across Lymphatic Endothelium [J].
Ahmed, S. Rumel ;
McGettrick, Helen M. ;
Yates, Clara M. ;
Buckley, Christopher D. ;
Ratcliffe, Marianne J. ;
Nash, Gerard B. ;
Rainger, G. Ed .
JOURNAL OF IMMUNOLOGY, 2011, 187 (03) :1432-1439
[2]  
Ajuebor MN, 1999, J IMMUNOL, V162, P1685
[3]   Lymphoid neogenesis in chronic inflammatory diseases [J].
Aloisi, F ;
Pujol-Borrell, R .
NATURE REVIEWS IMMUNOLOGY, 2006, 6 (03) :205-217
[4]   MODULATION OF ENDOTHELIAL-CELL SURFACE GLYCOCONJUGATE EXPRESSION BY ORGAN-DERIVED BIOMATRICES [J].
AUGUSTINVOSS, HG ;
JOHNSON, RC ;
PAULI, BU .
EXPERIMENTAL CELL RESEARCH, 1991, 192 (02) :346-351
[5]   Each step during transendothelial migration of flowing neutrophils is regulated by the stimulatory concentration of tumour necrosis factor-α [J].
Bahra, P ;
Rainger, GE ;
Wautier, JL ;
Luu, NT ;
Nash, GB .
CELL ADHESION AND COMMUNICATION, 1998, 6 (06) :491-501
[6]   Migration of leukocytes across an endothelium-epithelium bilayer as a model of renal interstitial inflammation [J].
Bijuklic, Klaudija ;
Jennings, Paul ;
Kountchev, Jordan ;
Hasslacher, Julia ;
Aydin, Sonia ;
Sturn, Daniel ;
Pfaller, Walter ;
Patsch, Josef R. ;
Joannidis, Michael .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2007, 293 (01) :C486-C492
[7]   Why don't we get more cancer? A proposed role of the microenvironment in restraining cancer progression [J].
Bissell, Mina J. ;
Hines, William C. .
NATURE MEDICINE, 2011, 17 (03) :320-329
[8]  
Bockman DE, 1997, INT J PANCREATOL, V21, P119
[9]   HUMAN NEUTROPHIL ADHERENCE TO LAMININ INVITRO - EVIDENCE FOR A DISTINCT NEUTROPHIL INTEGRIN RECEPTOR FOR LAMININ [J].
BOHNSACK, JF ;
AKIYAMA, SK ;
DAMSKY, CH ;
KNAPE, WA ;
ZIMMERMAN, GA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 171 (04) :1221-1237
[10]   CELL CONTACT BETWEEN T-CELLS AND SYNOVIAL FIBROBLASTS CAUSES INDUCTION OF ADHESION MOLECULES AND CYTOKINES [J].
BOMBARA, MP ;
WEBB, DL ;
CONRAD, P ;
MARLOR, CW ;
SARR, T ;
RANGES, GE ;
AUNE, TM ;
GREVE, JM ;
BLUE, ML .
JOURNAL OF LEUKOCYTE BIOLOGY, 1993, 54 (05) :399-406