The cavity-to-cavity migration of leukaemic cells through 3D honey-combed hydrogels with adjustable internal dimension and stiffness

被引:45
作者
da Silva, Joakim [1 ,2 ]
Lautenschlaeger, Franziska [1 ]
Sivaniah, Easan [1 ]
Guck, Jochen R. [1 ]
机构
[1] Univ Cambridge, Cavendish Lab, Dept Phys, Cambridge CB3 0HE, England
[2] KTH Royal Inst Technol, Dept Appl Phys, S-10691 Stockholm, Sweden
基金
英国工程与自然科学研究理事会;
关键词
Inverted colloidal crystal; Poly-acrylamide; Cell mechanics; Tissue invasion; Metastasis; ACUTE PROMYELOCYTIC LEUKEMIA; INVERTED COLLOIDAL CRYSTALS; TRANS-RETINOIC ACID; POLYMER; DIFFERENTIATION; NEUTROPHILS; ELASTICITY; MECHANICS; SCAFFOLDS; MATRICES;
D O I
10.1016/j.biomaterials.2009.11.105
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Whilst rigid, planar surfaces are often used to study cell migration, a physiological scenario requires three-dimensional (3D) scaffolds with tissue-like stiffness. This paper presents a method for fabricating periodic hydrogel scaffolds with a 3D honeycomb-like structure from colloidal crystal templates. The scaffolds, made of hydrogel-walled cavities interconnected by pores, have separately tuneable internal dimensions and adjustable gel stiffness down to that of soft tissues. In conjunction with confocal microscopy, these scaffolds were used to study the importance of cell compliance on invasive potential. Acute promyelocytic leukaemia (APL) cells were differentiated with all-trans retinoic acid (ATRA) and treated with paclitaxel. Their migration ability into the scaffolds' size-restricted pores, enabled by cell softening during ATRA differentiation, was significantly reduced by paclitaxel treatment, which interferes with cell shape recovery. These findings demonstrate the usability of the scaffolds for investigating factors that affect cell migration, and potentially other cell functions, in a realistic 3D tissue model. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2201 / 2208
页数:8
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