Aparicio-Yuste Raúl, Muenkel Marie, Clark Andrew G, Gómez-Benito María J, Bastounis Effie E
Department of Mechanical Engineering, Multiscale in Mechanical and Biological Engineering (M2BE), Instituto de Investigación en Ingeniería de Aragón (I3A), University of Zaragoza, Zaragoza, Spain.
Interfaculty Institute of Microbiology and Infection Medicine, Cluster of Excellence "Controlling Microbes to Fight Infections" (CMFI, EXC 2124), University of Tübingen, Tübingen, Germany.
Front Cell Dev Biol. 2022 Jun 22;10:912318. doi: 10.3389/fcell.2022.912318. eCollection 2022.
Cell competition refers to the mechanism whereby less fit cells ("losers") are sensed and eliminated by more fit neighboring cells ("winners") and arises during many processes including intracellular bacterial infection. Extracellular matrix (ECM) stiffness can regulate important cellular functions, such as motility, by modulating the physical forces that cells transduce and could thus modulate the output of cellular competitions. Herein, we employ a computational model to investigate the previously overlooked role of ECM stiffness in modulating the forceful extrusion of infected "loser" cells by uninfected "winner" cells. We find that increasing ECM stiffness promotes the collective squeezing and subsequent extrusion of infected cells due to differential cell displacements and cellular force generation. Moreover, we discover that an increase in the ratio of uninfected to infected cell stiffness as well as a smaller infection focus size, independently promote squeezing of infected cells, and this phenomenon is more prominent on stiffer compared to softer matrices. Our experimental findings validate the computational predictions by demonstrating increased collective cell extrusion on stiff matrices and glass as opposed to softer matrices, which is associated with decreased bacterial spread in the basal cell monolayer . Collectively, our results suggest that ECM stiffness plays a major role in modulating the competition between infected and uninfected cells, with stiffer matrices promoting this battle through differential modulation of cell mechanics between the two cell populations.
细胞竞争是指一种机制,即不太健康的细胞(“失败者”)会被更健康的相邻细胞(“胜利者”)识别并清除,这种现象在包括细胞内细菌感染在内的许多过程中都会出现。细胞外基质(ECM)的硬度可以通过调节细胞传导的物理力来调节重要的细胞功能,如运动能力,因此也可能调节细胞竞争的结果。在此,我们采用一个计算模型来研究ECM硬度在调节未感染的“胜利者”细胞对感染的“失败者”细胞进行强力挤压方面此前被忽视的作用。我们发现,由于细胞位移和细胞力产生的差异,增加ECM硬度会促进受感染细胞的集体挤压和随后的排出。此外,我们发现未感染细胞与感染细胞硬度之比的增加以及较小的感染灶尺寸会独立促进受感染细胞的挤压,并且与较软基质相比,这种现象在较硬基质上更为明显。我们的实验结果通过证明在硬基质和玻璃上相比软基质上集体细胞挤压增加来验证了计算预测,这与基底细胞单层中细菌传播的减少有关。总的来说,我们的结果表明ECM硬度在调节感染细胞和未感染细胞之间的竞争中起主要作用,较硬的基质通过对两种细胞群体之间细胞力学的差异调节来促进这场“战斗”。