Smyrek I, Mathew B, Fischer S C, Lissek S M, Becker S, Stelzer E H K
Physical Biology/Physikalische Biologie (IZN, FB 15), Buchmann Institute for Molecular Life Sciences (BMLS), Cluster of Excellence Frankfurt - Macromolecular Complexes (CEF - MC), Goethe Universität - Frankfurt am Main (Campus Riedberg), Max-von-Laue-Straße 15, D-60348 Frankfurt am Main, Germany.
Physical Biology/Physikalische Biologie (IZN, FB 15), Buchmann Institute for Molecular Life Sciences (BMLS), Cluster of Excellence Frankfurt - Macromolecular Complexes (CEF - MC), Goethe Universität - Frankfurt am Main (Campus Riedberg), Max-von-Laue-Straße 15, D-60348 Frankfurt am Main, Germany
Biol Open. 2019 Jan 24;8(1):bio037051. doi: 10.1242/bio.037051.
Spheroids resemble features of tissues and serve as model systems to study cell-cell and cell-ECM interactions in non-adhesive three-dimensional environments. Although it is generally accepted that mature spheroids resemble tissue properties very well, no studies relate different phases in the spheroid formation processes that contribute to tissue integrity. Tissue integrity involves the cellular processes adhesion formation, adhesion reinforcement, rearrangement as well as proliferation. They maintain the structure and function of tissues and, upon dysregulation, contribute to malignancy. We investigated spheroid formation dynamics in cell lines of different metastatic potential. We dissected spheroid formation into phases of aggregation, compaction and growth to identify the respective contributions of E-cadherin, actin, microtubules and FAK. E-cadherin, actin and microtubules drive the first two phases. Microtubules and FAK are involved in the proliferation phase. FAK activity correlates with the metastatic potential of the cells. A robust computational model based on a very large number of experiments reveals the temporal resolution of cell adhesion. Our results provide novel hypotheses to unveil the general mechanisms that contribute to tissue integrity.
球体类似于组织的特征,并作为模型系统用于研究在非粘附性三维环境中的细胞间和细胞与细胞外基质的相互作用。尽管人们普遍认为成熟的球体与组织特性非常相似,但尚无研究涉及球体形成过程中对组织完整性有贡献的不同阶段。组织完整性涉及细胞过程,如粘附形成、粘附增强、重排以及增殖。它们维持组织的结构和功能,一旦失调,就会导致恶性肿瘤。我们研究了具有不同转移潜能的细胞系中的球体形成动态。我们将球体形成分为聚集、压实和生长阶段,以确定E-钙粘蛋白、肌动蛋白、微管和粘着斑激酶(FAK)各自的作用。E-钙粘蛋白、肌动蛋白和微管驱动前两个阶段。微管和FAK参与增殖阶段。FAK活性与细胞的转移潜能相关。基于大量实验的强大计算模型揭示了细胞粘附的时间分辨率。我们的结果提供了新的假设,以揭示有助于组织完整性的一般机制。