J Korean Neurosurg Soc.  2019 Sep;62(5):493-501. 10.3340/jkns.2018.0222.

Human Induced Pluripotent Stem Cells: Clinical Significance and Applications in Neurologic Diseases

Affiliations
  • 1Department of Laboratory Medicine, Korea University Ansan Hospital, Ansan, Korea.
  • 2Department of Neurosurgery, Korea University Ansan Hospital, Ansan, Korea. neuron19@korea.ac.kr

Abstract

The generation of human induced pluripotent stem cells (iPSCs) from somatic cells using gene transfer opens new areas for precision medicine with personalized cell therapy and encourages the discovery of essential platforms for targeted drug development. iPSCs retain the genome of the donor, may regenerate indefinitely, and undergo differentiation into virtually any cell type of interest using a range of published protocols. There has been enormous interest among researchers regarding the application of iPSC technology to regenerative medicine and human disease modeling, in particular, modeling of neurologic diseases using patient-specific iPSCs. For instance, Parkinson's disease, Alzheimer's disease, and spinal cord injuries may be treated with iPSC therapy or replacement tissues obtained from iPSCs. In this review, we discuss the work so far on generation and characterization of iPSCs and focus on recent advances in the use of human iPSCs in clinical setting.

Keyword

Cell-based therapy; Induced pluripotent stem cells; Precision medicine

MeSH Terms

Cell- and Tissue-Based Therapy
Genome
Humans*
Induced Pluripotent Stem Cells*
Precision Medicine
Regenerative Medicine
Spinal Cord Injuries
Tissue Donors

Figure

  • Fig. 1. Isolation and characterization of pluripotent stem cells. ESC : embryonic stem cell, ICM : inner cell mass, iPSC : induced pluripotent stem cell, ASC : adult stem cell, CNS : central nervous system.

  • Fig. 2. Generation and applications of iPSCs from somatic cells. iPSCs can be applied in the field of clinical research for 1) patient-specific cell therapy, 2) drug screening, and 3) disease modeling. iPSC : induced pluripotent stem cell, Oct4 : octamer-binding transcription factor 4, Klf4 : Krüppel-like factor 4, Sox2 : SRY-box containing gene 2, c-Myc : cytoplasmic Myc gene.

  • Fig. 3. Safety of cell reprogramming technologies.


Reference

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