TH2 cells and their cytokines regulate formation and function of lymphatic vessels

被引:79
作者
Shin, Kihyuk [1 ]
Kataru, Raghu P. [1 ]
Park, Hyeung Ju [1 ]
Kwon, Bo-In [1 ]
Kim, Tae Woo [1 ]
Hong, Young Kwon [2 ]
Lee, Seung-Hyo [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Inst BioCentury, Biomed Res Ctr, Grad Sch Med Sci & Engn, Taejon 305701, South Korea
[2] Univ S Carolina, Norris Comprehens Canc Ctr, Los Angeles, CA 90033 USA
关键词
DISEASE; LYMPHANGIOGENESIS; VASCULATURE; INTERLEUKIN-4; ANGIOGENESIS; ENDOTHELIUM; RECEPTOR; SYSTEM; DIFFERENTIATION; INFLAMMATION;
D O I
10.1038/ncomms7196
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lymphatic vessels (LVs) are critical for immune surveillance and involved in the pathogenesis of diverse diseases. LV density is increased during inflammation; however, little is known about how the resolution of LVs is controlled in different inflammatory conditions. Here we show the negative effects of T helper type 2 (T(H)2) cells and their cytokines on LV formation. IL-4 and IL-13 downregulate essential transcription factors of lymphatic endothelial cells (LECs) and inhibit tube formation. Co-culture of LECs with T(H)2 cells also inhibits tube formation, but this effect is fully reversed by interleukin (IL)-4 and/or IL-13 neutralization. Furthermore, the in vivo blockade of IL-4 and/or IL-13 in an asthma model not only increases the density but also enhances the function of lung LVs. These results demonstrate an anti-lymphangiogenic function of T(H)2 cells and their cytokines, suggesting a potential usefulness of IL-4 and/or IL-13 antagonist as therapeutic agents for allergic asthma through expanding LV mediated-enhanced antigen clearance from the inflammatory sites.
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页数:10
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