ibidi GmbH, Gräfelfing, Germany.
Institute of Complex Systems 7: Biomechanics, Forschungszentrum Jülich GmbH, Jülich, Germany.
PLoS One. 2019 Jul 17;14(7):e0219708. doi: 10.1371/journal.pone.0219708. eCollection 2019.
Considering the essential role of chemotaxis of adherent, slow-moving cells in processes such as tumor metastasis or wound healing, a detailed understanding of the mechanisms and cues that direct migration of cells through tissues is highly desirable. The state-of-the-art chemotaxis instruments (e.g. microfluidic-based devices, bridge assays) can generate well-defined, long-term stable chemical gradients, crucial for quantitative investigation of chemotaxis in slow-moving cells. However, the majority of chemotaxis tools are designed for the purpose of an in-depth, but labor-intensive analysis of migratory behavior of single cells. This is rather inefficient for applications requiring higher experimental throughput, as it is the case of e.g. clinical examinations, chemoattractant screening or studies of the chemotaxis-related signaling pathways based on subcellular perturbations. Here, we present an advanced migration assay for accelerated and facilitated evaluation of the chemotactic response of slow-moving cells. The revised chemotaxis chamber contains a hydrogel microstructure-the migration arena, designed to enable identification of chemotactic behavior of a cell population in respect to the end-point of the experiment. At the same time, the assay in form of a microscopy slide enables direct visualization of the cells in either 2D or 3D environment, and provides a stable and linear gradient of chemoattractant. We demonstrate the correctness of the assay on the model study of HT-1080 chemotaxis in 3D and on 2D surface. Finally, we apply the migration arena chemotaxis assay to screen for a chemoattractant of primary keratinocytes, cells that play a major role in wound healing, being responsible for skin re-epithelialization and a successful wound closure. In direction of new therapeutic strategies to promote wound repair, we identified the chemotactic activity of the epithelial growth factor receptor (EGFR) ligands EGF and TGFα (transforming growth factor α).
考虑到贴壁、缓慢移动的细胞的趋化作用在肿瘤转移或伤口愈合等过程中的重要作用,深入了解指导细胞通过组织迁移的机制和线索是非常可取的。最先进的趋化性仪器(例如基于微流控的设备、桥接测定法)可以产生定义明确、长期稳定的化学梯度,这对于定量研究缓慢移动细胞的趋化性至关重要。然而,大多数趋化性工具都是为了深入、但繁琐的单细胞迁移行为分析而设计的。对于需要更高实验通量的应用,例如临床检查、趋化剂筛选或基于亚细胞扰动的趋化相关信号通路研究,这是效率不高的。在这里,我们提出了一种先进的迁移测定法,用于加速和促进对缓慢移动细胞的趋化反应的评估。改良的趋化室包含一个水凝胶微结构——迁移竞技场,旨在能够识别细胞群体的趋化行为相对于实验终点。同时,作为显微镜载玻片的测定法可以直接在 2D 或 3D 环境下观察细胞,并提供稳定和线性的趋化剂梯度。我们在 HT-1080 细胞在 3D 和 2D 表面上的趋化性模型研究中验证了该测定法的正确性。最后,我们将迁移竞技场趋化性测定法应用于筛选原发性角质形成细胞的趋化剂,这些细胞在伤口愈合中起着重要作用,负责皮肤再上皮化和成功的伤口闭合。在促进伤口修复的新治疗策略方向上,我们鉴定了表皮生长因子受体 (EGFR) 配体 EGF 和 TGFα(转化生长因子 α)的趋化活性。