Disease-in-a-Dish The Contribution of Patient-Specific Induced Pluripotent Stem Cell Technology to Regenerative Rehabilitation

被引:21
作者
Mack, David L. [1 ,2 ]
Guan, Xuan [1 ,2 ,3 ]
Wagoner, Ashley [4 ,5 ]
Walker, Stephen J. [4 ,5 ]
Childers, Martin K. [1 ,2 ]
机构
[1] Univ Washington, Dept Rehabil Med, 850 Republican St, Seattle, WA 98109 USA
[2] Univ Washington, Inst Stem Cell & Regenerat Med, Sch Med, Seattle, WA 98109 USA
[3] Wake Forest Univ Hlth Sci, Dept Physiol & Pharmacol, Winston Salem, NC USA
[4] Wake Forest Univ Hlth Sci, Dept Neurosci, Winston Salem, NC USA
[5] Wake Forest Univ Hlth Sci, Wake Forest Inst Regenerat Med, Winston Salem, NC USA
关键词
Induced Pluripotent Stem Cells; Neuromuscular Diseases; Autism; Duchenne Muscular Dystrophy; Cardiomyopathy; Drug Screening; Disease in a Dish; Disease Modeling; AUTISM SPECTRUM DISORDERS; DUCHENNE MUSCULAR-DYSTROPHY; 22Q13 DELETION SYNDROME; GASTROINTESTINAL PROBLEMS; DIRECTED DIFFERENTIATION; SOMATIC-CELLS; COPY NUMBER; TROPONIN-I; CHILDREN; SHANK3;
D O I
10.1097/PHM.0000000000000141
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
Advances in regenerative medicine technologies will lead to dramatic changes in how patients in rehabilitation medicine clinics are treated in the upcoming decades. The multidisciplinary field of regenerative medicine is developing new tools for disease modeling and drug discovery based on induced pluripotent stem cells. This approach capitalizes on the idea of personalized medicine by using the patient's own cells to discover new drugs, increasing the likelihood of a favorable outcome. The search for compounds that can correct disease defects in the culture dish is a conceptual departure from how drug screens were done in the past. This system proposes a closed loop from sample collection from the diseased patient, to in vitro disease model, to drug discovery and Food and Drug Administration approval, to delivering that drug back to the same patient. Here, recent progress in patient-specific induced pluripotent stem cell derivation, directed differentiation toward diseased cell types, and how those cells can be used for high-throughput drug screens are reviewed. Given that restoration of normal function is a driving force in rehabilitation medicine, the authors believe that this drug discovery platform focusing on phenotypic rescue will become a key contributor to therapeutic compounds in regenerative rehabilitation.
引用
收藏
页码:S155 / S168
页数:14
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