Department of Medical and Molecular Genetics, Division of Nephrology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Department of Biochemistry and Molecular Biology, Division of Nephrology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Kidney Int. 2021 Mar;99(3):598-608. doi: 10.1016/j.kint.2020.10.024. Epub 2020 Nov 4.
Fibroblast Growth Factor 23 (FGF23) is a bone-derived hormone that reduces kidney phosphate reabsorption and 1,25(OH)2 vitamin D synthesis via its required co-receptor alpha-Klotho. To identify novel genes that could serve as targets to control FGF23-mediated mineral metabolism, gene array and single-cell RNA sequencing were performed in wild type mouse kidneys. Gene array demonstrated that heparin-binding EGF-like growth factor (HBEGF) was significantly up-regulated following one-hour FGF23 treatment of wild type mice. Mice injected with HBEGF had phenotypes consistent with partial FGF23-mimetic activity including robust induction of Egr1, and increased Cyp24a1 mRNAs. Single cell RNA sequencing showed overlapping HBEGF and EGF-receptor expression mostly in the proximal tubule, and alpha-Klotho expression in proximal and distal tubule segments. In alpha-Klotho-null mice devoid of canonical FGF23 signaling, HBEGF injections significantly increased Egr1 and Cyp24a1 with correction of basally elevated Cyp27b1. Additionally, mice placed on a phosphate deficient diet to suppress FGF23 had endogenously increased Cyp27b1 mRNA, which was rescued in mice receiving HBEGF. In HEK293 cells with stable alpha-Klotho expression, FGF23 and HBEGF increased CYP24A1 mRNA expression. HBEGF, but not FGF23 bioactivity was blocked with EGF-receptor inhibition. Thus, our findings support that the paracrine/autocrine factor HBEGF could play novel roles in controlling genes downstream of FGF23 via targeting common signaling pathways.
成纤维细胞生长因子 23(FGF23)是一种骨源激素,通过其必需的共同受体α-Klotho 降低肾脏磷酸盐重吸收和 1,25(OH)2 维生素 D 的合成。为了鉴定可作为控制 FGF23 介导的矿物质代谢的新靶标,在野生型小鼠肾脏中进行了基因阵列和单细胞 RNA 测序。基因阵列表明,肝素结合表皮生长因子样生长因子(HBEGF)在野生型小鼠接受 FGF23 治疗 1 小时后显著上调。注射 HBEGF 的小鼠表现出与部分 FGF23 模拟活性一致的表型,包括 Egr1 的强烈诱导和 Cyp24a1 mRNA 的增加。单细胞 RNA 测序显示 HBEGF 和表皮生长因子受体的表达大部分重叠,主要在近端小管中,α-Klotho 表达在近端和远端小管段。在缺乏典型 FGF23 信号的α-Klotho 缺失小鼠中,HBEGF 注射显着增加 Egr1 和 Cyp24a1,并纠正了基础升高的 Cyp27b1。此外,在接受 HBEGF 注射的小鼠中,放置在磷酸盐缺乏饮食以抑制 FGF23 的小鼠内源性增加 Cyp27b1 mRNA。在稳定表达α-Klotho 的 HEK293 细胞中,FGF23 和 HBEGF 增加 CYP24A1 mRNA 表达。用表皮生长因子受体抑制阻断 HBEGF,但不是 FGF23 生物活性。因此,我们的研究结果表明,旁分泌/自分泌因子 HBEGF 可能通过靶向共同的信号通路在控制 FGF23 下游的基因方面发挥新的作用。