EphA2 is a functional receptor for the growth factor progranulin

被引:102
作者
Neill, Thomas [1 ,2 ]
Buraschi, Simone [1 ,2 ]
Goyal, Atul [1 ,2 ]
Sharpe, Catherine [1 ,2 ]
Natkanski, Elizabeth [1 ,2 ]
Schaefer, Liliana [5 ]
Morrione, Andrea [3 ,4 ]
Iozzo, Renato V. [1 ,2 ]
机构
[1] Thomas Jefferson Univ, Sidney Kimmel Med Coll, Dept Pathol Anat & Cell Biol, Sidney Kimmel Canc Ctr, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Sidney Kimmel Med Coll, Canc Cell Biol & Signaling Program, Sidney Kimmel Canc Ctr, Philadelphia, PA 19107 USA
[3] Thomas Jefferson Univ, Sidney Kimmel Med Coll, Dept Urol, Sidney Kimmel Canc Ctr, Philadelphia, PA 19107 USA
[4] Thomas Jefferson Univ, Sidney Kimmel Med Coll, Biol Prostate Canc Program, Sidney Kimmel Canc Ctr, Philadelphia, PA 19107 USA
[5] Goethe Univ, Inst Pharmacol & Toxicol, D-60323 Frankfurt, Germany
基金
美国国家卫生研究院;
关键词
FRONTOTEMPORAL LOBAR DEGENERATION; GRANULIN-EPITHELIN PRECURSOR; TYROSINE KINASE; CANCER-CELLS; BLADDER-CANCER; METASTATIC PROGRESSION; MONOMERIC EPHRINA1; TUMOR ANGIOGENESIS; ADIPOSE-TISSUE; TNF RECEPTORS;
D O I
10.1083/jcb.201603079
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Although the growth factor progranulin was discovered more than two decades ago, the functional receptor remains elusive. Here, we discovered that EphA2, a member of the large family of Ephrin receptor tyrosine kinases, is a functional signaling receptor for progranulin. Recombinant progranulin bound with high affinity to EphA2 in both solid phase and solution. Interaction of progranulin with EphA2 caused prolonged activation of the receptor, downstream stimulation of mitogen-activated protein kinase and Akt, and promotion of capillary morphogenesis. Furthermore, we found an autoregulatory mechanism of progranulin whereby a feed-forward loop occurred in an EphA2-dependent manner that was independent of the endocytic receptor sortilin. The discovery of a functional signaling receptor for progranulin offers a new avenue for understanding the underlying mode of action of progranulin in cancer progression, tumor angiogenesis, and perhaps neurodegenerative diseases.
引用
收藏
页码:687 / 703
页数:17
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