Doolin Mary T, Moriarty Rebecca A, Stroka Kimberly M
Fischell Department of Bioengineering, University of Maryland, College Park, College Park, MD, United States.
Maryland Biophysics Program, University of Maryland, College Park, College Park, MD, United States.
Front Physiol. 2020 Apr 24;11:365. doi: 10.3389/fphys.2020.00365. eCollection 2020.
Mesenchymal stem cells (MSCs) and tumor cells have the unique capability to migrate out of their native environment and either home or metastasize, respectively, through extremely heterogeneous environments to a distant location. Once there, they can either aid in tissue regrowth or impart an immunomodulatory effect in the case of MSCs, or form secondary tumors in the case of tumor cells. During these journeys, cells experience physically confining forces that impinge on the cell body and the nucleus, ultimately causing a multitude of cellular changes. Most drastically, confining individual MSCs within hydrogels or confining monolayers of MSCs within agarose wells can sway MSC lineage commitment, while applying a confining compressive stress to metastatic tumor cells can increase their invasiveness. In this review, we seek to understand the signaling cascades that occur as cells sense confining forces and how that translates to behavioral changes, including elongated and multinucleated cell morphologies, novel migrational mechanisms, and altered gene expression, leading to a unique MSC secretome that could hold great promise for anti-inflammatory treatments. Through comparison of these altered behaviors, we aim to discern how MSCs alter their lineage selection, while tumor cells may become more aggressive and invasive. Synthesizing this information can be useful for employing MSCs for therapeutic approaches through systemic injections or tissue engineered grafts, and developing improved strategies for metastatic cancer therapies.
间充质干细胞(MSCs)和肿瘤细胞具有独特的能力,能够从其原生环境中迁移出来,分别通过极其异质的环境归巢或转移到远处。一旦到达那里,它们要么有助于组织再生,如间充质干细胞那样发挥免疫调节作用,要么如肿瘤细胞那样形成继发性肿瘤。在这些迁移过程中,细胞会经历作用于细胞体和细胞核的物理限制力,最终导致多种细胞变化。最显著的是,将单个间充质干细胞限制在水凝胶中或在琼脂糖孔中限制间充质干细胞单层,可影响间充质干细胞的谱系定向,而对转移性肿瘤细胞施加限制压缩应力可增加其侵袭性。在本综述中,我们试图了解细胞感知限制力时发生的信号级联反应,以及这如何转化为行为变化,包括细胞形态拉长和多核化、新型迁移机制以及基因表达改变,从而产生一种对抗炎治疗可能具有巨大潜力的独特间充质干细胞分泌组。通过比较这些改变的行为,我们旨在辨别间充质干细胞如何改变其谱系选择,而肿瘤细胞可能变得更具侵袭性。综合这些信息对于通过全身注射或组织工程移植物将间充质干细胞用于治疗方法,以及开发改进的转移性癌症治疗策略可能是有用的。