Institute of Biochemistry and Molecular Biology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Department of Nephrology, Chang Gung Memorial Hospital, Keelung, Taiwan.
Biochem J. 2021 Jun 25;478(12):2321-2337. doi: 10.1042/BCJ20210070.
LMBD1 was previously demonstrated to regulate the endocytosis of insulin receptor on the cell surface and to mediate the export of cobalamin from the lysosomes to the cytosol, but little is known about its function in mitosis. In this study, interactome analysis data indicate that LMBD1 is involved in cytoskeleton regulation. Both immunoprecipitation and GST pulldown assays demonstrated the association of LMBD1 with tubulin. Immunofluorescence staining also showed the colocalization of LMBD1 with microtubule in both interphase and mitotic cells. LMBD1 specifically accelerates microtubule assembly dynamics in vitro and antagonizes the microtubule-disruptive effect of vinblastine. In addition, LMBRD1-knockdown impairs mitotic spindle formation, inhibits tubulin polymerization, and diminishes the mitosis-associated tubulin acetylation. The reduced acetylation can be reversed by ectopic expression of LMBD1 protein. These results suggest that LMBD1 protein stabilizes microtubule intermediates. Furthermore, embryonic fibroblasts derived from Lmbrd1 heterozygous knockout mice showed abnormality in microtubule formation, mitosis, and cell growth. Taken together, LMBD1 plays a pivotal role in regulating microtubule assembly that is essential for the process of cell mitosis.
LMBD1 先前被证明可以调节细胞表面胰岛素受体的内吞作用,并介导钴胺素从溶酶体向细胞质的输出,但关于其在有丝分裂中的功能知之甚少。在这项研究中,相互作用组分析数据表明 LMBD1 参与细胞骨架的调节。免疫沉淀和 GST 下拉测定均表明 LMBD1 与微管蛋白的结合。免疫荧光染色也显示 LMBD1 在有丝分裂间期和有丝分裂细胞中与微管的共定位。LMBD1 特异性地加速体外微管组装动力学,并拮抗长春花碱对微管的破坏作用。此外,LMBRD1 敲低会损害有丝分裂纺锤体的形成,抑制微管蛋白聚合,并减少与有丝分裂相关的微管乙酰化。通过异位表达 LMBD1 蛋白可以逆转减少的乙酰化。这些结果表明,LMBD1 蛋白稳定微管中间体。此外,来自 Lmbrd1 杂合敲除小鼠的胚胎成纤维细胞显示微管形成、有丝分裂和细胞生长异常。总之,LMBD1 在调节微管组装中起着关键作用,这对于细胞有丝分裂过程是必不可少的。