CXCL17 Is a Major Chemotactic Factor for Lung Macrophages

被引:44
作者
Burkhardt, Amanda M. [1 ,2 ]
Maravillas-Montero, Jose L. [1 ,2 ]
Carnevale, Christina D. [1 ,2 ]
Vilches-Cisneros, Natalia [3 ]
Flores, Juan P. [3 ]
Hevezi, Peter A. [1 ,2 ]
Zlotnik, Albert [1 ,2 ]
机构
[1] Univ Calif Irvine, Sch Med, Dept Physiol & Biophys, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Inst Immunol, Irvine, CA 92697 USA
[3] Univ Nuevo Leon, Dept Pathol Anat & Cytopathol, Monterrey 64460, Nuevo Leon, Mexico
基金
美国国家卫生研究院;
关键词
CHEMOKINE RECEPTOR; ALVEOLAR MACROPHAGES; MICE LACKING; GERM-FREE; LEUKOCYTE EXTRAVASATION; GENE-EXPRESSION; CELL-MIGRATION; CUTTING EDGE; PURIFICATION; ORIGIN;
D O I
10.4049/jimmunol.1400551
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chemokines are a superfamily of chemotactic cytokines that direct the movement of cells throughout the body under homeostatic and inflammatory conditions. The mucosal chemokine CXCL17 was the last ligand of this superfamily to be characterized. Several recent studies have provided greater insight into the basic biology of this chemokine and have implicated CXCL17 in several human diseases. We sought to better characterize CXCL17's activity in vivo. To this end, we analyzed its chemoattractant properties in vivo and characterized a Cxcl17(-/-) mouse. This mouse has a significantly reduced number of macrophages in its lungs compared with wild-type mice. In addition, we observed a concurrent increase in a new population of macrophage-like cells that are F4/80+CDllc(mid). These results indicate that CXCL17 is a novel macrophage chemoattractant that operates in mucosal tissues. Given the importance of macrophages in inflammation, these observations strongly suggest that CXCL17 is a major regulator of mucosal inflammatory responses.
引用
收藏
页码:1468 / 1474
页数:7
相关论文
共 62 条
[11]   Cutting edge: Ectopic expression of the chemokine TCA4/SLC is sufficient to trigger lymphoid neogenesis [J].
Fan, L ;
Reilly, CR ;
Luo, Y ;
Dorf, ME ;
Lo, D .
JOURNAL OF IMMUNOLOGY, 2000, 164 (08) :3955-3959
[12]   The nuclear receptor Rev-erbα is a liver X receptor (LXR) target gene driving a negative feedback loop on select LXR-induced pathways in human macrophages [J].
Fontaine, Coralie ;
Rigamonti, Elena ;
Pourcet, Benoit ;
Duez, Helene ;
Duhem, Christian ;
Fruchart, Jean-Charles ;
Chinetti-Gbaguidi, Giulia ;
Staels, Bart .
MOLECULAR ENDOCRINOLOGY, 2008, 22 (08) :1797-1811
[13]   CCR7 coordinates the primary immune response by establishing functional microenvironments in secondary lymphoid organs [J].
Förster, R ;
Schubel, A ;
Breitfeld, D ;
Kremmer, E ;
Renner-Müller, I ;
Wolf, E ;
Lipp, M .
CELL, 1999, 99 (01) :23-33
[14]   Gene-expression profiles and transcriptional regulatory pathways that underlie the identity and diversity of mouse tissue macrophages [J].
Gautier, Emmanuel L. ;
Shay, Tal ;
Miller, Jennifer ;
Greter, Melanie ;
Jakubzick, Claudia ;
Ivanov, Stoyan ;
Helft, Julie ;
Chow, Andrew ;
Elpek, Kutlu G. ;
Gordonov, Simon ;
Mazloom, Amin R. ;
Ma'ayan, Avi ;
Chua, Wei-Jen ;
Hansen, Ted H. ;
Turley, Shannon J. ;
Merad, Miriam ;
Randolph, Gwendalyn J. .
NATURE IMMUNOLOGY, 2012, 13 (11) :1118-1128
[15]   ORIGIN OF ALVEOLAR MACROPHAGES IN MOUSE RADIATION CHIMERAS [J].
GODLESKI, JJ ;
BRAIN, JD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1972, 136 (03) :630-&
[16]  
Grieder FB, 2002, COMPARATIVE MED, V52, P203
[17]   The Immunological Genome Project: networks of gene expression in immune cells [J].
Heng, Tracy S. P. ;
Painter, Michio W. .
NATURE IMMUNOLOGY, 2008, 9 (10) :1091-1094
[18]   CXCL17 and ICAM2 Are Associated With a Potential Anti-Tumor Immune Response in Early Intraepithelial Stages of Human Pancreatic Carcinogenesis [J].
Hiraoka, Nobuyoshi ;
Yamazaki-Itoh, Rie ;
Ino, Yoshinori ;
Mizuguchi, Yasunori ;
Yamada, Tesshi ;
Hirohashi, Setsuo ;
Kanai, Yae .
GASTROENTEROLOGY, 2011, 140 (01) :310-+
[19]   Alveolar macrophages: plasticity in a tissue-specific context [J].
Hussell, Tracy ;
Bell, Thomas J. .
NATURE REVIEWS IMMUNOLOGY, 2014, 14 (02) :81-93
[20]   Functional diversity and plasticity of human dendritic cell subsets [J].
Ito, T ;
Liu, YJ ;
Kadowaki, N .
INTERNATIONAL JOURNAL OF HEMATOLOGY, 2005, 81 (03) :188-196