Bouju Agathe, Nusse Roel, Wu Peng V
Department of Developmental Biology, Howard Hughes Medical Institute, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA; Sorbonne University, Paris, France.
Department of Developmental Biology, Howard Hughes Medical Institute, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Differentiation. 2024 Nov-Dec;140:100816. doi: 10.1016/j.diff.2024.100816. Epub 2024 Oct 24.
Fibroblast Growth Factor 19 (FGF19) is a member of the Fibroblast Growth Factor (FGF) family, known for its role in various cellular processes including embryonic development and metabolic regulation. FGF19 functions as an endocrine factor, influencing energy balance, bile acid synthesis, glucose and lipid metabolism, as well as cell proliferation. FGF19 has a conserved structure typical of FGFs but exhibits unique features. Unlike most FGFs, which act locally, FGF19 travels through the bloodstream to distant targets including the liver. Its interaction with the β-Klotho (KLB) co-receptor and FGF Receptor 4 (FGFR4) in hepatocytes or FGFR1c in extrahepatic tissues initiates signaling cascades crucial for its biological functions. Although the mouse ortholog, FGF15, diverges significantly from human FGF19 in protein sequence and receptor binding, studies of FGF15-deficient mice have led to a better understanding of the proteins' role in bile acid regulation, metabolism, and embryonic development. Overexpression studies in transgenic mice have further revealed roles in not only ameliorating metabolic diseases but also in promoting hepatocyte proliferation and tumorigenesis. This review summarizes the gene and protein structure of FGF19/15, its expression patterns, phenotypes in mutant models, and implication in human diseases, providing insights into potential therapeutic strategies targeting the FGF19 signaling pathway.
成纤维细胞生长因子19(FGF19)是成纤维细胞生长因子(FGF)家族的成员之一,因其在包括胚胎发育和代谢调节在内的各种细胞过程中发挥的作用而闻名。FGF19作为一种内分泌因子,影响能量平衡、胆汁酸合成、葡萄糖和脂质代谢以及细胞增殖。FGF19具有FGFs典型的保守结构,但也表现出独特的特征。与大多数在局部起作用的FGFs不同,FGF19通过血液循环到达包括肝脏在内的远处靶标。它与肝细胞中的β-klotho(KLB)共受体和FGF受体4(FGFR4)或肝外组织中的FGFR1c相互作用,启动对其生物学功能至关重要的信号级联反应。尽管小鼠直系同源物FGF15在蛋白质序列和受体结合方面与人类FGF19有很大差异,但对FGF15缺陷小鼠的研究有助于更好地理解这些蛋白质在胆汁酸调节、代谢和胚胎发育中的作用。在转基因小鼠中的过表达研究进一步揭示了其不仅在改善代谢疾病方面的作用,还在促进肝细胞增殖和肿瘤发生方面的作用。这篇综述总结了FGF19/15的基因和蛋白质结构、其表达模式、突变模型中的表型以及在人类疾病中的意义,为针对FGF19信号通路的潜在治疗策略提供了见解。