期刊
FASEB JOURNAL
卷 21, 期 3, 页码 754-765出版社
WILEY
DOI: 10.1096/fj.06-6847com
关键词
lentivirus; LGR7; blood vessel; MMP-9
Hormone antagonists can be effective tools to delineate receptor signaling pathways and their resulting downstream physiological actions. Mutation of the receptor binding domain (RBD) of human H2 relaxin (Delta H2) impaired its biological function as measured by cAMP signaling. In a competition assay, Delta H2 exhibited antagonistic activity by blocking recombinant H2 relaxin from binding to receptors on THP-1 cells. In a flow cytometry-based binding assay, Delta H2 demonstrated weak binding to 293T cells expressing the LGR7 receptor in the presence of biotinylated H2 relaxin. When human prostate cancer cell lines (PC-3 and LNCaP) were engineered to overexpress eGFP, wildtype (WT) H2, or Delta H2, and subsequently implanted into NOD/SCID mice, tumor xenografts overexpressing Delta H2 displayed smaller volumes compared to H2 and eGFP controls. Plasma osmolality readings and microvessel density and area assessment suggest that Delta H2 modulates physiological parameters in vivo. In a second murine model, intratumoral injections of lentivectors engineered to express Delta H2/eGFP led to suppressed tumor growth compared to controls. This study provides further evidence supporting a role for H2 relaxin in prostate tumor growth. More importantly, we report how mutation of the H2 relaxin RBD confers the hormone derivative with antagonistic properties, offering a novel reagent for relaxin research.
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