Identification of PLXDC1 and PLXDC2 as the Transmembrane Receptors for the Multifunctional Factor PEDF

被引:63
作者
Cheng, Guo [1 ,2 ]
Zhong, Ming [1 ,2 ]
Kawaguchi, Riki [1 ,2 ]
Kassai, Miki [1 ,2 ]
Al-Ubaidi, Muayyad [3 ]
Deng, Jun [1 ,2 ]
Ter-Stepanian, Mariam [1 ,2 ]
Sun, Hui [1 ,2 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Howard Hughes Med Inst, Dept Physiol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Jules Stein Eye Inst, Los Angeles, CA 90095 USA
[3] Univ Oklahoma, Hlth Sci Ctr, Dept Cell Biol, Oklahoma City, OK USA
关键词
EPITHELIUM-DERIVED FACTOR; HUMAN GROWTH-HORMONE; ENDOTHELIAL-CELLS; FACTOR EXPRESSION; AQUEOUS-HUMOR; PROSTATE; PROTEIN; CANCER; NEOVASCULARIZATION; PURIFICATION;
D O I
10.7554/eLife.05401
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
Pigment Epithelium Derived Factor (PEDF) is a secreted factor that has broad biological activities. It was first identified as a neurotrophic factor and later as the most potent natural antiangiogenic factor, a stem cell niche factor, and an inhibitor of cancer cell growth. Numerous animal models demonstrated its therapeutic value in treating blinding diseases and diverse cancer types. A long-standing challenge is to reveal how PEDF acts on its target cells and the identities of the cell-surface receptors responsible for its activities. Here we report the identification of transmembrane proteins PLXDC1 and PLXDC2 as cell-surface receptors for PEDF. Using distinct cellular models, we demonstrate their cell type-specific receptor activities through loss of function and gain of function studies. Our experiments suggest that PEDF receptors form homooligomers under basal conditions, and PEDF dissociates the homooligomer to activate the receptors. Mutations in the intracellular domain can have profound effects on receptor activities.
引用
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页数:38
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