Haridas Parvathi, Browning Alexander P, McGovern Jacqui A, Sean McElwain D L, Simpson Matthew J
Institute of Health and Biomedical Innovation, Queensland University of Technology (QUT), Kelvin Grove, 4059, Australia.
School of Mathematical Sciences, QUT, Brisbane, 4001, Australia.
BMC Syst Biol. 2018 Mar 27;12(1):34. doi: 10.1186/s12918-018-0559-9.
Melanoma can be diagnosed by identifying nests of cells on the skin surface. Understanding the processes that drive nest formation is important as these processes could be potential targets for new cancer drugs. Cell proliferation and cell migration are two potential mechanisms that could conceivably drive melanoma nest formation. However, it is unclear which one of these two putative mechanisms plays a dominant role in driving nest formation.
We use a suite of three-dimensional (3D) experiments in human skin tissue and a parallel series of 3D individual-based simulations to explore whether cell migration or cell proliferation plays a dominant role in nest formation. In the experiments we measure nest formation in populations of irradiated (non-proliferative) and non-irradiated (proliferative) melanoma cells, cultured together with primary keratinocyte and fibroblast cells on a 3D experimental human skin model. Results show that nest size depends on initial cell number and is driven primarily by cell proliferation rather than cell migration.
Nest size depends on cell number, and is driven primarily by cell proliferation rather than cell migration. All experimental results are consistent with simulation data from a 3D individual based model (IBM) of cell migration and cell proliferation.
黑色素瘤可通过识别皮肤表面的细胞巢来诊断。了解驱动细胞巢形成的过程很重要,因为这些过程可能是新型抗癌药物的潜在靶点。细胞增殖和细胞迁移是两种可能驱动黑色素瘤细胞巢形成的潜在机制。然而,尚不清楚这两种假定机制中的哪一种在驱动细胞巢形成中起主导作用。
我们在人体皮肤组织中进行了一系列三维(3D)实验,并进行了一系列基于个体的3D平行模拟,以探究细胞迁移或细胞增殖在细胞巢形成中是否起主导作用。在实验中,我们在三维人体皮肤模型上,测量与原代角质形成细胞和成纤维细胞共同培养的受辐照(非增殖性)和未受辐照(增殖性)黑色素瘤细胞群体中的细胞巢形成情况。结果表明,细胞巢大小取决于初始细胞数量,并且主要由细胞增殖而非细胞迁移驱动。
细胞巢大小取决于细胞数量,并且主要由细胞增殖而非细胞迁移驱动。所有实验结果均与基于细胞迁移和细胞增殖的三维个体模型(IBM)的模拟数据一致。