3D extracellular matrix microenvironment in bioengineered tissue models of primary pediatric and adult brain tumors

被引:90
作者
Sood, Disha [1 ]
Tang-Schomer, Min [2 ,3 ]
Pouli, Dimitra [1 ,4 ,5 ]
Mizzoni, Craig [1 ]
Raia, Nicole [1 ]
Tai, Albert [6 ]
Arkun, Knarik [7 ]
Wu, Julian [8 ]
Black, Lauren D., III [1 ]
Scheffler, Bjorn [9 ,10 ,11 ]
Georgakoudi, Irene [1 ]
Steindler, Dennis A. [9 ,12 ]
Kaplan, David L. [1 ]
机构
[1] Tufts Univ, Dept Biomed Engn, Medford, MA 02155 USA
[2] Jackson Lab Genom Med, Farmington, CT 06032 USA
[3] Connecticut Childrens Med Ctr, Harford, CT 06106 USA
[4] Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02114 USA
[5] Harvard Med Sch, Boston, MA 02114 USA
[6] Tufts Univ, Sch Med, Genom Core, Boston, MA 02111 USA
[7] Tufts Med Ctr, Dept Pathol & Lab Med, Boston, MA 02111 USA
[8] Tufts Med Ctr, Dept Neurosurg, Boston, MA 02111 USA
[9] Univ Florida, McKnight Brain Inst, Dept Neurosci, Gainesville, FL 32610 USA
[10] German Canc Consortium DKTK, DKFZ Div Translat Oncol Neurooncol, Heidelberg, Germany
[11] Univ Hosp Essen, Essen, Germany
[12] Tufts Univ, Neurosci & Aging Lab, Jean Mayer USDA Human Nutr Res Ctr Aging, Boston, MA 02111 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
CELL LINES; GLIOMA; PROTEOGLYCANS; FLUORESCENCE; METALLOPROTEINASES; HETEROGENEITY; EPENDYMOMA; RESISTANCE; INHIBITION; EXPRESSION;
D O I
10.1038/s41467-019-12420-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dynamic alterations in the unique brain extracellular matrix (ECM) are involved in malignant brain tumors. Yet studies of brain ECM roles in tumor cell behavior have been difficult due to lack of access to the human brain. We present a tunable 3D bioengineered brain tissue platform by integrating microenvironmental cues of native brain-derived ECMs and live imaging to systematically evaluate patient-derived brain tumor responses. Using pediatric ependymoma and adult glioblastoma as examples, the 3D brain ECM-containing microenvironment with a balance of cell-cell and cell-matrix interactions supports distinctive phenotypes associated with tumor type-specific and ECM-dependent patterns in the tumor cells' transcriptomic and release profiles. Label-free metabolic imaging of the composite model structure identifies metabolically distinct sub-populations within a tumor type and captures extracellular lipid-containing droplets with potential implications in drug response. The versatile bioengineered 3D tumor tissue system sets the stage for mechanistic studies deciphering microenvironmental role in brain tumor progression.
引用
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页数:14
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