ECM Mechano-Sensing Regulates Cytoskeleton Assembly and Receptor-Mediated Endocytosis of Nanoparticles

被引:22
作者
Panzetta, Valeria [1 ]
Guarnieri, Daniela [1 ]
Paciello, Antonio [1 ]
Della Sala, Francesca [1 ]
Muscetti, Ornella [1 ]
Raiola, Luca [1 ]
Netti, Paolo [1 ,2 ,3 ]
Fusco, Sabato [1 ,2 ,3 ]
机构
[1] Ist Italiano Tecnol, IIT CRIB, Ctr Adv Biomat Hlth Care, Lgo Barsanti & Matteucci 53, I-80125 Naples, Italy
[2] Univ Naples Federico II, Interdisciplinary Res Ctr Biomat, CRIB, I-80125 Naples, Italy
[3] Univ Naples Federico II, Dept Chem Mat & Ind Prod Engn, I-80125 Naples, Italy
来源
ACS BIOMATERIALS SCIENCE & ENGINEERING | 2017年 / 3卷 / 08期
关键词
cell mechanics; nanoparticles uptake; ECM stiffness; cytoskeleton assembly; receptor mediated endocytosis; BLOOD-BRAIN-BARRIER; CELL-ADHESION; DRUG-DELIVERY; CYTOCHALASIN-D; TUMOR-CELLS; IN-VITRO; INTEGRINS; CANCER; STIFFNESS; RGD;
D O I
10.1021/acsbiomaterials.7b00018
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
It is possible to create sophisticated and target specific devices for nanomedicine thanks to technological advances in the engineering of nanomaterials. 'When on target, these nanocarriers often have to be internalized by cells in order to accomplish their diagnostic or therapeutic function. Therefore, the control of such uptake mechanism by active targeting strategy has today become the new challenge in nanoparticle designing. It is also well-known that cells are able to sense and respond to the local physical environment and that the substrate stiffness, and not only the nanoparticle design, influences the cellular internalization mechanisms. In this frame, our work reports on the cyclic relationship among substrate stiffness, cell cytoskeleton assembly and internalization mechanism. Nanoparticles uptake has been investigated in terms of the mechanics of cell environment, the resulting cytoskeleton activity and the opportunity of activate molecular specific molecular pathways during the internalization process. To this aim, the surface of 100 nm polystyrene nanoparticles was decorated with a tripeptide (RGD and a scrambled version as a control), which was able to activate an internalization pathway directly correlated to the dynamics of the cell cytoskeleton, in turn, directly correlated to the elastic modulus of the substrates. We found that the substrate stiffness modulates the uptake of nanoparticles by regulating structural parameters of bEnd.3 cells as spreading, volume, focal adhesion, and mechanics. In fact, the nanoparticles were internalized in larger amounts both when decorated with RGD, which activated an internalization pathway directly correlated to the cell cytoskeleton, and when cells resided on stiffer material that, in turn, promoted the formation of a more structured cytoskeleton. This evidence indicates the directive role of the mechanical environment on cellular uptake of nanoparticles, contributing new insights to the rational design and development of novel nanocarrier systems.
引用
收藏
页码:1586 / 1594
页数:9
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