Mechanosensing of Mechanical Confinement by Mesenchymal-Like Cells

被引:22
作者
Doolin, Mary T. [1 ]
Moriarty, Rebecca A. [1 ]
Stroka, Kimberly M. [1 ,2 ,3 ,4 ]
机构
[1] Univ Maryland, Fischell Dept Bioengn, College Pk, MD 20742 USA
[2] Univ Maryland, Maryland Biophys Program, College Pk, MD 20742 USA
[3] Univ Maryland, Ctr Stem Cell Biol & Regenerat Med, Baltimore, MD 21201 USA
[4] Univ Maryland, Marlene & Stewart Greenebaum Comprehens Canc Ctr, Baltimore, MD 21201 USA
关键词
cancer; stem cell; confinement; migration; differentiation; NUCLEAR-ENVELOPE RUPTURE; CANCER STEM-CELLS; OSTEOGENIC DIFFERENTIATION; MATRIX ELASTICITY; 3D MIGRATION; CONTACT GUIDANCE; TUMOR-CELLS; BONE-MARROW; DNA-DAMAGE; INVASION;
D O I
10.3389/fphys.2020.00365
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
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.
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页数:19
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