Embedding of Precision-Cut Lung Slices in Engineered Hydrogel Biomaterials Supports Extended Ex Vivo Culture

被引:38
作者
Bailey, Kolene E. [1 ]
Pino, Christopher [2 ]
Lennon, Mallory L. [2 ]
Lyons, Anne [2 ]
Jacot, Jeffrey G. [2 ]
Lammers, Steven R. [2 ]
Konigshoff, Melanie [1 ]
Magin, Chelsea M. [1 ,2 ]
机构
[1] Univ Colorado, Div Pulm Sci & Crit Care Med, Dept Med, Aurora, CO 80045 USA
[2] Univ Colorado, Dept Bioengn, Aurora, CO 80045 USA
基金
美国国家卫生研究院;
关键词
precision-cut lung slice; hydrogel; biomaterial; three-dimensional printing; pulmonary disease modeling; RESPONSES; ACTIVATION; PEPTIDES; ADHESION; HYPOXIA; DISEASE;
D O I
10.1165/rcmb.2019-0232MA
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Maintaining the three-dimensional architecture and cellular complexity of lung tissue ex vivo can enable elucidation of the cellular and molecular pathways underlying chronic pulmonary diseases. Precision-cut lung slices (PCLS) are one human-lung model with the potential to support critical mechanistic studies and early drug discovery. However, many studies report short culture times of 7-10 days. Here, we systematically evaluated poly(ethylene glycol)-based hydrogel platforms for the encapsulation of PCLS. We demonstrated the ability to support ex vivo culture of embedded PCLS for at least 21 days compared with control PCLS floating in media. These customized hydrogels maintained PCLS architecture (no difference), viability (4.7-fold increase, P < 0.0001), and cellular phenotype as measured by SFTPC (1.8-fold increase, P < 0.0001) and vimentin expression (no change) compared with nonencapsulated controls. Collectively, these results demonstrate that hydrogel biomaterials support the extended culture times required to study chronic pulmonary diseases ex vivo using PCLS technology.
引用
收藏
页码:14 / 22
页数:9
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