生物
有丝分裂
细胞生物学
微管
细胞生长
胶质母细胞瘤
肿瘤进展
调节器
胚胎干细胞
癌症研究
遗传学
基因
作者
Allison E. Cherry,Juan Jesus Vicente,Cong Xu,Richard S. Morrison,Shao‐En Ong,Linda Wordeman,Nephi Stella
出处
期刊:Glia
[Wiley]
日期:2019-05-06
卷期号:67 (8): 1558-1570
被引量:23
摘要
GPR124 is involved in embryonic development and remains expressed by select organs. The importance of GPR124 during development suggests that its aberrant expression might participate in tumor growth. Here we show that both increases and decreases in GPR124 expression in glioblastoma cells reduce cell proliferation by differentially altering the duration mitotic progression. Using mass spectrometry-based proteomics, we discovered that GPR124 interacts with ch-TOG, a known regulator of both microtubule (MT)-plus-end assembly and mitotic progression. Accordingly, changes in GPR124 expression and ch-TOG similarly affect MT assembly measured by real-time microscopy in cells. Our study describes a novel molecular interaction involving GPR124 and ch-TOG at the plasma membrane that controls glioblastoma cell proliferation by modifying MT assembly rates and controlling the progression of distinct phases of mitosis.
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