Reconstituting Organ-Level Lung Functions on a Chip

被引:3001
作者
Huh, Dongeun [1 ,2 ,3 ,4 ]
Matthews, Benjamin D. [2 ,3 ,4 ,5 ]
Mammoto, Akiko [2 ,3 ,4 ]
Montoya-Zavala, Martin [1 ,2 ,3 ,4 ]
Hsin, Hong Yuan [2 ,3 ,4 ]
Ingber, Donald E. [1 ,2 ,3 ,4 ,6 ]
机构
[1] Harvard Univ, Wyss Inst Biologically Inspired Engn, Boston, MA 02115 USA
[2] Childrens Hosp, Dept Pathol, Vasc Biol Program, Boston, MA 02115 USA
[3] Childrens Hosp, Dept Surg, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA 02115 USA
[5] Childrens Hosp, Dept Med, Boston, MA 02115 USA
[6] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
关键词
HUMAN ENDOTHELIAL-CELLS; IN-VITRO MODEL; SILICA NANOPARTICLES; CULTURE; BARRIER; MECHANISMS; SYSTEMS; TISSUE; TOXICITY; CHANNELS;
D O I
10.1126/science.1188302
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
Here, we describe a biomimetic microsystem that reconstitutes the critical functional alveolar-capillary interface of the human lung. This bioinspired microdevice reproduces complex integrated organ-level responses to bacteria and inflammatory cytokines introduced into the alveolar space. In nanotoxicology studies, this lung mimic revealed that cyclic mechanical strain accentuates toxic and inflammatory responses of the lung to silica nanoparticles. Mechanical strain also enhances epithelial and endothelial uptake of nanoparticulates and stimulates their transport into the underlying microvascular channel. Similar effects of physiological breathing on nanoparticle absorption are observed in whole mouse lung. Mechanically active "organ-on-a-chip" microdevices that reconstitute tissue-tissue interfaces critical to organ function may therefore expand the capabilities of cell culture models and provide low-cost alternatives to animal and clinical studies for drug screening and toxicology applications.
引用
收藏
页码:1662 / 1668
页数:7
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