Department of Biological Sciences, Hunter College of City University, New York, New York, USA.
Biology Program, The Graduate Center City University, New York, New York, USA.
J Physiol. 2024 Sep;602(17):4097-4110. doi: 10.1113/JP286313. Epub 2024 Jul 31.
Since their discovery nearly 30 years ago, fibroblast growth factor homologous factors (FHFs) are now known to control the functionality of excitable tissues through a range of mechanisms. Nervous and cardiac system dysfunctions are caused by loss- or gain-of-function mutations in FHF genes. The best understood 'canonical' targets for FHF action are voltage-gated sodium channels, and recent studies have expanded the repertoire of ways that FHFs modulate sodium channel gating. Additional 'non-canonical' functions of FHFs in excitable and non-excitable cells, including cancer cells, have been reported over the past dozen years. This review summarizes and evaluates reported canonical and non-canonical FHF functions.
自近 30 年前发现以来,成纤维细胞生长因子同源因子(FHFs)现已被证实通过一系列机制控制兴奋组织的功能。FHF 基因突变导致神经和心脏系统功能障碍,功能丧失或获得。FHF 作用的最佳“经典”靶标是电压门控钠离子通道,最近的研究扩展了 FHF 调节钠离子通道门控的方式。过去十几年间,已有报道称 FHF 在兴奋和非兴奋细胞(包括癌细胞)中具有其他“非经典”功能。本综述总结和评估了报道的经典和非经典 FHF 功能。