The neutrophil protein CD177 is a novel PDPN receptor that regulates human cancer-associated fibroblast physiology

被引:10
作者
Astarita, Jillian L. [1 ]
Keerthivasan, Shilpa [1 ]
Husain, Bushra [2 ]
Senbabaoglu, Yasin [3 ]
Verschueren, Erik [2 ]
Gierke, Sarah [4 ]
Pham, Victoria C. [2 ]
Peterson, Sean M. [2 ]
Chalouni, Cecile [4 ]
Pierce, Andrew A. [5 ]
Lill, Jennie R. [2 ]
Gonzalez, Lino C. [2 ]
Martinez-Martin, Nadia [2 ]
Turley, Shannon J. [1 ]
机构
[1] Genentech Inc, Dept Canc Immunol, San Francisco, CA 94080 USA
[2] Genentech Inc, Dept Microchem Prote & Lipid, San Francisco, CA 94080 USA
[3] Genentech Inc, Dept Bioinformat & Computat Biol, San Francisco, CA 94080 USA
[4] Genentech Inc, Ctr Adv Light Microscopy, San Francisco, CA 94080 USA
[5] Genentech Inc, Dept Pathol Res, San Francisco, CA 94080 USA
关键词
PREDICTS POOR-PROGNOSIS; MATRIX STIFFNESS; PODOPLANIN; CELLS; EXPRESSION; PHOSPHORYLATION; PLATFORM; IMPACT; TARGET; STAT3;
D O I
10.1371/journal.pone.0260800
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
The cancer-associated fibroblast (CAF) marker podoplanin (PDPN) is generally correlated with poor clinical outcomes in cancer patients and thus represents a promising therapeutic target. Despite its biomedical relevance, basic aspects of PDPN biology such as its cellular functions and cell surface ligands remain poorly uncharacterized, thus challenging drug development. Here, we utilize a high throughput platform to elucidate the PDPN cell surface interactome, and uncover the neutrophil protein CD177 as a new binding partner. Quantitative proteomics analysis of the CAF phosphoproteome reveals a role for PDPN in cell signaling, growth and actomyosin contractility, among other processes. Moreover, cellular assays demonstrate that CD177 is a functional antagonist, recapitulating the phenotype observed in PDPN-deficient CAFs. In sum, starting from the unbiased elucidation of the PDPN co-receptome, our work provides insights into PDPN functions and reveals the PDPN/CD177 axis as a possible modulator of fibroblast physiology in the tumor microenvironment.
引用
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页数:23
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