| Literature DB >> 31058365 |
Allison E Cherry1, Juan Jesus Vicente2, Cong Xu1, Richard S Morrison3, Shao-En Ong1, Linda Wordeman2, Nephi Stella1,4.
Abstract
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.Entities:
Keywords: G protein-coupled receptors and microtubules; cell proliferation; glioblastomas
Mesh:
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Year: 2019 PMID: 31058365 PMCID: PMC6557680 DOI: 10.1002/glia.23628
Source DB: PubMed Journal: Glia ISSN: 0894-1491 Impact factor: 7.452