Cytokine signaling regulating adipose stromal cell trafficking

被引:9
|
作者
Zhang, Yan [1 ]
Kolonin, Mikhail G. [1 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Ctr Stem Cell & Regenerat Med, Brown Fdn Inst Mol Med, Houston, TX 77030 USA
关键词
adipose stromal cell; cytokine; chemokine; CXCL1; cancer; interleukin-22; receptor; obesity; STEM-CELLS; PROGENITOR-CELLS; TISSUE CELLS; CANCER; OBESITY; RECEPTOR; LIPOTRANSFER; SURFACE; GROWTH; TUMORS;
D O I
10.1080/21623945.2016.1220452
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adipocyte progenitors, known as adipose stromal cells (ASC), can become mobilized, recruited by tumors, and contribute to cancer progression. Mechanisms underlying ASC trafficking have remained obscure. We recently reported that CXCL1 expressed by cancer cells chemoattracts ASC expressing CXCR1 in obesity. As a candidate mechanism of CXCL1 activation, we identified interleukin (IL)-22, systemic circulation of which is increased in obesity. It has been reported that IL-22 signaling through IL-22R is upstream of CXCL1. Here, we provide evidence that IL-22 expression by leukocytes infiltrating WAT and IL-22R expression by tumors is obesity-dependent. We propose that obesity-associated adipocyte death and the resulting recruitment of leukocytes triggers the IL-22 signaling cascade that induces CXCL1 secretion by cancer cells responsible for ASC trafficking to tumors.
引用
收藏
页码:369 / 374
页数:6
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