Irene Monleón-Guinot, Lucía Bravo-Baranda, Lara Milián, María Sancho-Tello, Mauro Llop-Miguel, José Marcelo Galbis, Antonio Cremades, Carmen Carda, Manuel Mata
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In this work, we aimed to investigate the involvement of epithelial and stromal cancer cells in growth, cell migration, and epithelial-to-mesenchymal transition (EMT) in a 3D in vitro model consisting of cell spheroids cultured in a type I collagen scaffold.</p><p><strong>Methods: </strong>Spheroids were manufactured using different combinations of epithelial cells, particularly H460 and H1792 cell lines, with cancer-associated fibroblasts and normal fibroblasts, both isolated from adenocarcinoma patients. We evaluated the morphology of the spheroids by analysis of F-actin and pankeratin with confocal microscopy. We determined the ultrastructure of cells in the spheroids by transmission electron microscopy and the expression of CDH1, CDH2, and VIM by RT-PCR.</p><p><strong>Results: </strong>We observed that, on the one hand, the type of epithelial cell influences the morphology of spheroids. Stromal cells stimulated spheroid growth and cell dissemination through the collagen matrix, either alone or organized in branches with a nucleus of epithelial cells preceded by fibroblast cells. They also induced the appearance of new cell groups in the scaffold and the presence of EMT markers.</p><p><strong>Conclusion: </strong>The results presented here indicate the participation of both epithelial and stromal cells in the control of spheroid self-organization. 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引用次数: 0
摘要
导言/目的:众所周知,肿瘤微环境在肿瘤进展过程中发挥着重要作用。然而,人们对这一过程的具体机制仍不甚了解,需要对控制肺癌肿瘤进展的因素进行更多的研究。在这项工作中,我们旨在研究上皮细胞和基质癌细胞参与生长、细胞迁移和上皮细胞向间质转化(EMT)的三维体外模型,该模型由在 I 型胶原支架中培养的细胞球组成:我们用上皮细胞(尤其是 H460 和 H1792 细胞系)与癌症相关成纤维细胞(CAFs)和正常成纤维细胞(NFs)的不同组合制造了球形细胞,这两种细胞都是从腺癌患者体内分离出来的。我们用共聚焦显微镜分析了 F-肌动蛋白和泛影葡聚糖,评估了球形细胞的形态。我们用透射电子显微镜测定了球体内细胞的超微结构,并用 RT-PCR 检测了 CDH1、CDH2 和 VIM 的表达:结果:我们观察到,一方面,上皮细胞的类型会影响球形细胞的形态。基质细胞刺激球体生长,并使细胞通过胶原基质扩散。它们还诱导支架中出现新的细胞群,并出现 EMT 标记:本文的研究结果表明,上皮细胞和基质细胞都参与了球体自组织的控制。本文提出的实验模型虽然是初步的,但有助于研究肺癌肿瘤进展的某些相关方面。
Cancer Epithelial Cells Participate in the Self-Organization of Lung Tumor Spheroids: A Morphological Approach.
Introduction/aims: The tumor microenvironment is known to play an important role in tumor progression. However, the specific mechanisms underlying this process are still not known in detail and more research is needed on the elements that control tumor progression in lung cancer. In this work, we aimed to investigate the involvement of epithelial and stromal cancer cells in growth, cell migration, and epithelial-to-mesenchymal transition (EMT) in a 3D in vitro model consisting of cell spheroids cultured in a type I collagen scaffold.
Methods: Spheroids were manufactured using different combinations of epithelial cells, particularly H460 and H1792 cell lines, with cancer-associated fibroblasts and normal fibroblasts, both isolated from adenocarcinoma patients. We evaluated the morphology of the spheroids by analysis of F-actin and pankeratin with confocal microscopy. We determined the ultrastructure of cells in the spheroids by transmission electron microscopy and the expression of CDH1, CDH2, and VIM by RT-PCR.
Results: We observed that, on the one hand, the type of epithelial cell influences the morphology of spheroids. Stromal cells stimulated spheroid growth and cell dissemination through the collagen matrix, either alone or organized in branches with a nucleus of epithelial cells preceded by fibroblast cells. They also induced the appearance of new cell groups in the scaffold and the presence of EMT markers.
Conclusion: The results presented here indicate the participation of both epithelial and stromal cells in the control of spheroid self-organization. The experimental model proposed here, although preliminary, is useful for the study of some aspects related to tumor progression in lung cancer.