3D microvascular model recapitulates the diffuse large B-cell lymphoma tumor microenvironment in vitro

被引:68
作者
Mannino, Robert G. [1 ,2 ,3 ,4 ,5 ,6 ]
Santiago-Miranda, Adriana N. [1 ,2 ,3 ]
Pradhan, Pallab [1 ,2 ,3 ]
Qiu, Yongzhi [1 ,2 ,3 ,4 ,5 ,6 ]
Mejias, Joscelyn C. [1 ,2 ,3 ]
Neelapu, Sattva S. [7 ]
Roy, Krishnendu [1 ,2 ,3 ]
Lam, Wilbur A. [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Georgia Tech, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30332 USA
[2] Emory Univ, Atlanta, GA 30322 USA
[3] Georgia Inst Technol, Parker H Petit Inst Bioengn & Biosci, Atlanta, GA 30332 USA
[4] Emory Univ, Sch Med, Dept Pediat, Div Pediat Hematol Oncol, Atlanta, GA USA
[5] Childrens Healthcare Atlanta, Aflac Canc & Blood Disorders Ctr, Atlanta, GA USA
[6] Georgia Inst Technol, Inst Elect & Nanotechnol, Atlanta, GA 30332 USA
[7] Univ Texas MD Anderson Canc Ctr, Div Canc Med, Dept Lymphoma & Myeloma, Houston, TX 77030 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
NON-HODGKINS-LYMPHOMA; ALLOGENEIC TRANSPLANTATION; EBMT REGISTRY; ORGANS; METASTASIS; CULTURE;
D O I
10.1039/c6lc01204c
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Diffuse large B-cell lymphoma (DLBCL) is an aggressive cancer that affects similar to 22000 people in the United States yearly. Understanding the complex cellular interactions of the tumor microenvironment is critical to the success and development of DLBCL treatment strategies. In vitro platforms that successfully model the complex tumor microenvironment without introducing the variability of in vivo systems are vital for understanding these interactions. To date, no such in vitro model exists that can accurately recapitulate the interactions that occur between immune cells, cancer cells, and endothelial cells in the tumor microenvironment of DLBCL. To that end, we developed a lymphoma-on-chip model consisting of a hydrogel based tumor model traversed by a vascularized, perfusable, round microchannel that successfully recapitulates key complexities and interactions of the in vivo tumor microenvironment in vitro. We have shown that the perfusion capabilities of this technique allow us to study targeted treatment strategies, as well as to model the diffusion of infused reagents spatiotemporally. Furthermore, this model employs a novel fabrication technique that utilizes common laboratory materials, and allows for the microfabrication of multiplex microvascular environments without the need for advanced microfabrication facilities. Through our facile microfabrication process, we are able to achieve micro vessels within a tumor model that are highly reliable and precise over the length of the vessel. Overall, we have developed a tool that enables researchers from many diverse disciplines to study previously inaccessible aspects of the DLBCL tumor microenvironment, with profound implications for drug delivery and design.
引用
收藏
页码:407 / 414
页数:8
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