A novel device to concurrently assess leukocyte extravasation and interstitial migration within a defined 3D environment

被引:19
作者
Molteni, Raffaella [1 ]
Bianchi, Elena [2 ]
Patete, Paolo [3 ]
Fabbri, Monica [1 ]
Baroni, Guido [3 ]
Dubini, Gabriele [2 ]
Pardi, Ruggero [1 ,4 ]
机构
[1] Ist Sci San Raffaele, Leukocyte Biol Unit, Div Immunol Transplantat & Infect Dis, I-20132 Milan, Italy
[2] Politecn Milan, Lab Biol Struct Mech, Dept Chem Mat & Chem Engn, I-20133 Milan, Italy
[3] Politecn Milan, Dept Elect Informat & Bioengn, I-20133 Milan, Italy
[4] Univ Vita Salute San Raffaele, Sch Med, Milan, Italy
关键词
TRANSENDOTHELIAL MIGRATION; POLYMORPHONUCLEAR LEUKOCYTES; NEUTROPHIL CHEMOTAXIS; INTEGRIN ACTIVATION; ENDOTHELIAL-CELLS; VENULAR WALLS; IN-VIVO; ADHESION; FLOW; GRADIENTS;
D O I
10.1039/c4lc00741g
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Leukocyte extravasation and interstitial migration are key events during inflammation. Traditional in vitro techniques address only specific steps of cell recruitment to tissues and fail to recapitulate the whole process in an appropriate three-dimensional (3D) microenvironment. Herein, we describe a device that enables us to qualitatively and quantitatively assess in 4D the interdependent steps underlying leukocyte trafficking in a close-to-physiology in vitro context. Real-time tracking of cells, from initial adhesion to the endothelium and subsequent diapedesis to interstitial migration towards the source of the chemoattractant within the 3D collagen matrix, is enabled by the use of optically transparent porous membranes laid over the matrix. Unique features of the device, such as the use of non-planar surfaces and the contribution of physiological flow to the establishment of a persistent chemoattractant gradient, were assessed by numerical simulations and validated by proof-of-concept, simultaneous testing of differentially treated primary mouse neutrophils. This microfluidic platform offers new and versatile tools to thoroughly investigate the stepwise process of circulating cell recruitment to target tissues in vitro and to test novel therapeutics targeting various steps of the process.
引用
收藏
页码:195 / 207
页数:13
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