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Extracellular protonation modulates cell-cell interaction mechanics and tissue invasion in human melanoma cells

机译:细胞外质子调节人类黑素瘤细胞中的细胞间相互作用机制和组织入侵。

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摘要

Detachment of cells from the primary tumour precedes metastatic progression by facilitating cell release into the tissue. Solid tumours exhibit altered pH homeostasis with extracellular acidification. In human melanoma, the Na+/H+ exchanger NHE1 is an important modifier of the tumour nanoenvironment. Here we tested the modulation of cell-cell-adhesion by extracellular pH and NHE1. MV3 tumour spheroids embedded in a collagen matrix unravelled the efficacy of cell-cell contact loosening and 3D emigration into an environment mimicking physiological confinement. Adhesive interaction strength between individual MV3 cells was quantified using atomic force microscopy and validated by multicellular aggregation assays. Extracellular acidification from pHe7.4 to 6.4 decreases cell migration and invasion but increases single cell detachment from the spheroids. Acidification and NHE1 overexpression both reduce cell-cell adhesion strength, indicated by reduced maximum pulling forces and adhesion energies. Multicellular aggregation and spheroid formation are strongly impaired under acidification or NHE1 overexpression. We show a clear dependence of melanoma cell-cell adhesion on pHe and NHE1 as a modulator. These effects are opposite to cell-matrix interactions that are strengthened by protons extruded via NHE1. We conclude that these opposite effects of NHE1 act synergistically during the metastatic cascade.
机译:通过促进细胞释放到组织中,将细胞从原发肿瘤中分离出来就可以进行转移。实体瘤表现出胞外酸化改变的pH稳态。在人类黑素瘤中,Na + / H + 交换子NHE1是肿瘤纳米环境的重要修饰剂。在这里,我们测试了细胞外pH和NHE1对细胞-细胞粘附的调节。嵌入胶原蛋白基质中的MV3肿瘤球体揭示了细胞间接触松弛和3D迁移到模拟生理限制的环境中的功效。使用原子力显微镜对单个MV3细胞之间的粘附相互作用强度进行定量,并通过多细胞聚集测定法对其进行验证。从pHe7.4到6.4的细胞外酸化作用会减少细胞迁移和侵袭,但会增加单个细胞与球体的分离。酸化和NHE1过表达均会降低细胞间的粘附强度,这可通过降低最大拉力和粘附能来表明。在酸化或NHE1过表达下,多细胞聚集和球体形成受到严重损害。我们显示对pHe和NHE1作为调节剂的黑色素瘤细胞粘附的明确依赖性。这些作用与通过NHE1挤出的质子加强的细胞-基质相互作用相反。我们得出结论,在转移级联过程中,NHE1的这些相反作用协同作用。

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