Correlative Imaging of Three-Dimensional Cell Culture on Opaque Bioscaffolds for Tissue Engineering Applications

被引:2
|
作者
Sawyer, Mone't [1 ]
Eixenberger, Josh [2 ,3 ]
Nielson, Olivia [4 ]
Manzi, Jacob [5 ]
Francis, Cadre [6 ]
Montenegro-Brown, Raquel [6 ,7 ]
Subbaraman, Harish [5 ]
Estrada, David [3 ,6 ,7 ,8 ]
机构
[1] Boise State Univ, Biomed Engn Doctoral Program, Boise, ID 83725 USA
[2] Boise State Univ, Dept Phys, Boise, ID 83725 USA
[3] Boise State Univ, Ctr Adv Energy Studies, Boise, ID 83725 USA
[4] Univ Idaho, Dept Chem & Biol Engn, Moscow, ID 83844 USA
[5] Oregon State Univ, Sch Elect Engn & Comp Sci, Corvallis, OR 97331 USA
[6] Boise State Univ, Micron Sch Mat Sci & Engn, Boise, ID 83725 USA
[7] Boise State Univ, Ctr Atom Thin Multifunct Coatings, Boise, ID 83725 USA
[8] Idaho Natl Lab, Idaho Falls, ID 83401 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
graphene foam; tissue engineering; correlativemicroscopy; microcomputed tomography; gold nanoparticles; ARTICULAR-CARTILAGE; SCAFFOLDS; BIOMATERIALS;
D O I
10.1021/acsabm.3c00408
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Three-dimensional (3D) tissue engineering (TE) is a prospective treatment that can be used to restore or replace damaged musculoskeletal tissues, such as articular cartilage. However, current challenges in TE include identifying materials that are biocompatible and have properties that closely match the mechanical properties and cellular microenvironment of the target tissue. Visualization and analysis of potential 3D porous scaffolds as well as the associated cell growth and proliferation characteristics present additional problems. This is particularly challenging for opaque scaffolds using standard optical imaging techniques. Here, we use graphene foam (GF) as a 3D porous biocompatible substrate, which is scalable, reproducible, and a suitable environment for ATDC5 cell growth and chondrogenic differentiation. ATDC5 cells are cultured, maintained, and stained with a combination of fluorophores and gold nanoparticles to enable correlative microscopic characterization techniques, which elucidate the effect of GF properties on cell behavior in a 3D environment. Most importantly, the staining protocol allows for direct imaging of cell growth and proliferation on opaque scaffolds using X-ray MicroCT, including imaging growth of cells within the hollow GF branches, which is not possible with standard fluorescence and electron microscopy techniques.
引用
收藏
页码:3717 / 3725
页数:9
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