4.6 Review

The translational potential of human induced pluripotent stem cells for clinical neurology

期刊

CELL BIOLOGY AND TOXICOLOGY
卷 33, 期 2, 页码 129-144

出版社

SPRINGER
DOI: 10.1007/s10565-016-9372-7

关键词

Cellular therapy; Disease modeling; Drug discovery; Human induced pluripotent stem cells (hiPSCs); Neurology; Translational medicine

资金

  1. MRC Clinical Research Training Fellowship [MR/N020820/1]
  2. Wellcome Trust Intermediate Clinical Fellow [101149/Z/13/Z]
  3. Anne Rowling Fellow in Regenerative Neurology
  4. Medical Research Council [MR/N020820/1] Funding Source: researchfish
  5. Wellcome Trust [101149/Z/13/Z] Funding Source: researchfish
  6. MRC [MR/N020820/1] Funding Source: UKRI
  7. Wellcome Trust [101149/Z/13/Z] Funding Source: Wellcome Trust

向作者/读者索取更多资源

The induced pluripotent state represents a decade-old Nobel prize-winning discovery. Human-induced pluripotent stem cells (hiPSCs) are generated by the nuclear reprogramming of any somatic cell using a variety of established but evolving methods. This approach offers medical science unparalleled experimental opportunity to model an individual patient's disease in a dish. HiPSCs permit developmentally rationalized directed differentiation into any cell type, which express donor cell mutation(s) at pathophysiological levels and thus hold considerable potential for disease modeling, drug discovery, and potentially cell-based therapies. This review will focus on the translational potential of hiPSCs in clinical neurology and the importance of integrating this approach with complementary model systems to increase the translational yield of preclinical testing for the benefit of patients. This strategy is particularly important given the expected increase in prevalence of neurodegenerative disease, which poses a major burden to global health over the coming decades.

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