A Long-Living Bioengineered Neural Tissue Platform to Study Neurodegeneration

被引:34
|
作者
Rouleau, Nicolas [1 ,2 ,3 ]
Cantley, William L. [1 ,2 ]
Liaudanskaya, Volha [1 ,2 ]
Berk, Alexander [1 ]
Du, Chuang [1 ,2 ]
Rusk, William [1 ]
Peirent, Emily [1 ]
Koester, Cole [1 ]
Nieland, Thomas J. F. [1 ,2 ]
Kaplan, David L. [1 ,2 ,3 ]
机构
[1] Tufts Univ, Dept Biomed Engn, Sch Engn, Sci & Technol Ctr, 4 Colby St, Medford, MA 02155 USA
[2] Tufts Univ, Initiat Neural Sci Dis & Engn, Sci & Engn Complex,200 Coll Ave, Medford, MA 02155 USA
[3] Tufts Univ, Biol Dept, Allen Discovery Ctr, 200 Boston Ave Suite 4600, Medford, MA 02155 USA
关键词
Alzheimer's disease; bioengineering; biomaterials; induced pluripotent stem cells; neurodegeneration; MILD COGNITIVE IMPAIRMENT; ALZHEIMERS-DISEASE; HUMAN BRAIN; MATURATION; DEMENTIA; MODEL; SILK; CHILDHOOD; ORGANOIDS; RATIO;
D O I
10.1002/mabi.202000004
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
The prevalence of dementia and other neurodegenerative diseases continues to rise as age demographics in the population shift, inspiring the development of long-term tissue culture systems with which to study chronic brain disease. Here, it is investigated whether a 3D bioengineered neural tissue model derived from human induced pluripotent stem cells (hiPSCs) can remain stable and functional for multiple years in culture. Silk-based scaffolds are seeded with neurons and glial cells derived from hiPSCs supplied by human donors who are either healthy or have been diagnosed with Alzheimer's disease. Cell retention and markers of stress remain stable for over 2 years. Diseased samples display decreased spontaneous electrical activity and a subset displays sporadic-like indicators of increased pathological beta-amyloid and tau markers characteristic of Alzheimer's disease with concomitant increases in oxidative stress. It can be concluded that the long-term stability of the platform is suited to study chronic brain disease including neurodegeneration.
引用
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页数:8
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