Institute of Molecular and Cell Biology, Singapore 138673, Singapore.
Centre for Mechanochemical Cell Biology, Warwick Medical School, Coventry CV4 7AL, UK.
Cells. 2019 Aug 16;8(8):915. doi: 10.3390/cells8080915.
Various growth factors and full-length cell surface receptors such as EGFR are translocated from the cell surface to the nucleoplasm, baffling cell biologists to the mechanisms and functions of this process. Elevated levels of nuclear EGFR correlate with poor prognosis in various cancers. In recent years, nuclear EGFR has been implicated in regulating gene transcription, cell proliferation and DNA damage repair. Different models have been proposed to explain how the receptors are transported into the nucleus. However, a clear consensus has yet to be reached. Recently, we described the nuclear envelope associated endosomes (NAE) pathway, which delivers EGFR from the cell surface to the nucleus. This pathway involves transport, docking and fusion of NAEs with the outer membrane of the nuclear envelope. EGFR is then presumed to be transported through the nuclear pore complex, extracted from membranes and solubilised. The SUN1/2 nuclear envelope proteins, Importin-beta, nuclear pore complex proteins and the Sec61 translocon have been implicated in the process. While this framework can explain the cell surface to nucleus traffic of EGFR and other cell surface receptors, it raises several questions that we consider in this review, together with implications for health and disease.
各种生长因子和全长细胞表面受体(如 EGFR)从细胞表面转移到核质,这让细胞生物学家对这一过程的机制和功能感到困惑。核 EGFR 水平升高与各种癌症的预后不良相关。近年来,核 EGFR 被牵涉到调节基因转录、细胞增殖和 DNA 损伤修复。已经提出了不同的模型来解释受体如何被转运到核内。然而,目前尚未达成明确共识。最近,我们描述了核膜相关内体(NAE)途径,该途径将 EGFR 从细胞表面运送到细胞核。该途径涉及 NAEs 与核膜外膜的运输、对接和融合。然后推测 EGFR 通过核孔复合体被转运,从膜中提取并溶解。SUN1/2 核膜蛋白、Importin-beta、核孔复合体蛋白和 Sec61 易位酶已被牵涉到该过程中。虽然这个框架可以解释 EGFR 和其他细胞表面受体从细胞表面到细胞核的运输,但它提出了几个我们在这篇综述中考虑的问题,以及对健康和疾病的影响。