Frizzled-5: a high affinity receptor for secreted frizzled-related protein-2 activation of nuclear factor of activated T-cells c3 signaling to promote angiogenesis

被引:0
作者
Yuri K. Peterson
Patrick Nasarre
Ingrid V. Bonilla
Eleanor Hilliard
Jennifer Samples
Thomas A. Morinelli
Elizabeth G. Hill
Nancy Klauber-DeMore
机构
[1] Medical University of South Carolina,Department of Drug Discovery and Biomedical Sciences, College of Pharmacy
[2] Medical University of South Carolina,Department of Surgery
[3] University of North Carolina at Chapel Hill,Department of Surgery
[4] Medical University of South Carolina,Department of Medicine
[5] Medical University of South Carolina,Department of Public Health Science
来源
Angiogenesis | 2017年 / 20卷
关键词
Wnt; Calcium signaling; Endothelial cells; Calcineurin; Angiosarcoma;
D O I
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中图分类号
学科分类号
摘要
Secreted frizzled-related protein 2 (SFRP2) is a pro-angiogenic factor expressed in the vasculature of a wide variety of human tumors, and modulates angiogenesis via the calcineurin-dependent nuclear factor of activated T-cells cytoplasmic 3 (NFATc3) pathway in endothelial cells. However, until now, SFRP2 receptor for this pathway was unknown. In the present study, we first used amino acid alignments and molecular modeling to demonstrate that SFRP2 interaction with frizzled-5 (FZD5) is typical of Wnt/FZD family members. To confirm this interaction, we performed co-immunofluorescence, co-immunoprecipitation, and ELISA binding assays, which demonstrated SFRP2/FZD5 binding. Functional knock-down studies further revealed that FZD5 is necessary for SFRP2-induced tube formation and intracellular calcium flux in endothelial cells. Using protein analysis on endothelial cell nuclear extracts, we also discovered that FZD5 is required for SFRP2-induced activation of NFATc3. Our novel findings reveal that FZD5 is a receptor for SFRP2 and mediates SFRP2-induced angiogenesis via calcineurin/NFATc3 pathway in endothelial cells.
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页码:615 / 628
页数:13
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