Zhou Yi, Xu Meng-Fei, Chen Jie, Zhang Jing-Lian, Wang Xin-Yao, Huang Min-Hui, Wei Ya-Lan, She Zhen-Yu
Department of Cell Biology and Genetics, The School of Basic Medical Sciences, Fujian Medical University, Fuzhou, Fujian, 350122, China; Key Laboratory of Stem Cell Engineering and Regenerative Medicine, Fujian Province University, Fuzhou, Fujian, 350122, China.
Medical Research Center, Fujian Maternity and Child Health Hospital, Fuzhou, Fujian, 350001, China; College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou, Fujian, 350122, China.
Exp Cell Res. 2024 Mar 1;436(1):113975. doi: 10.1016/j.yexcr.2024.113975. Epub 2024 Feb 16.
Kinesin motors play a fundamental role in development by controlling intracellular transport, spindle assembly, and microtubule organization. In humans, patients carrying mutations in KIF11 suffer from an autosomal dominant inheritable disease called microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR). While mitotic functions of KIF11 proteins have been well documented in centrosome separation and spindle assembly, cellular mechanisms underlying KIF11 dysfunction and MCLMR remain unclear. In this study, we generate KIF11-inhibition chick and zebrafish models and find that KIF11 inhibition results in microcephaly, chorioretinopathy, and severe developmental defects in vivo. Notably, loss-of-function of KIF11 causes the formation of monopolar spindle and chromosome misalignment, which finally contribute to cell cycle arrest, chromosome instability, and cell death. Our results demonstrate that KIF11 is crucial for spindle assembly, chromosome alignment, and cell cycle progression of progenitor stem cells, indicating a potential link between polyploidy and MCLMR. Our data have revealed that KIF11 inhibition cause microcephaly, chorioretinopathy, and development disorders through the formation of monopolar spindle, polyploid, and cell cycle arrest.
驱动蛋白在通过控制细胞内运输、纺锤体组装和微管组织来进行发育过程中发挥着重要作用。在人类中,携带KIF11突变的患者患有常染色体显性遗传疾病,称为小头畸形,伴有或不伴有脉络膜视网膜病变、淋巴水肿或智力迟钝(MCLMR)。虽然KIF11蛋白的有丝分裂功能在中心体分离和纺锤体组装方面已有充分记录,但KIF11功能障碍和MCLMR的细胞机制仍不清楚。在本研究中,我们构建了KIF11抑制的鸡和斑马鱼模型,发现KIF11抑制在体内导致小头畸形、脉络膜视网膜病变和严重的发育缺陷。值得注意的是,KIF11功能丧失会导致单极纺锤体的形成和染色体排列错误,最终导致细胞周期停滞、染色体不稳定和细胞死亡。我们的结果表明,KIF11对于祖干细胞的纺锤体组装、染色体排列和细胞周期进程至关重要,这表明多倍体与MCLMR之间存在潜在联系。我们的数据显示,KIF11抑制通过单极纺锤体、多倍体的形成和细胞周期停滞导致小头畸形、脉络膜视网膜病变和发育障碍。