Multi- and inter-disciplinary science in personalized delivery of stem cells for tissue repair

Curr Stem Cell Res Ther. 2009 Jan;4(1):16-22. doi: 10.2174/157488809787169075.

Abstract

Stem cell therapy has a place for future application in the treatment of degenerative diseases. Regardless of the origin of the stem cell, when placed within a milieu of inflammatory mediator, they will show varied functions. This review focuses on human mesenchymal stem cells (MSCs) and discusses neuronal replacement using multi- and inter-disciplinary approaches. We caution the enthusiasm of scientists since there is always the potential for tumor formation, even for adult stem cells. The review places RE-1 silencing transcription factor (REST) gene as central to the understanding of stem cell behavior in the microenvironment of tissue injury. REST is relevant in the development of dopaminergic and peptidergic neurons from MSCs. Premature downregulation of REST by the pro-inflammatory mediator, IL-1alpha, can prematurely lead to the expression of neurotransmitters, which in turn, could develop rapid crosstalk with immune cells. In-depth inter- and multi-disciplinary research will lead to rapid and safe translation of MSCs to patients. An understanding of the changes induced in MSCs by cytokines and other mediators will establish future application of MSCs and other stem cells for safe and effective treatments. This study also alludes to the potential of personalized medicine through engineering and mathematics.

Publication types

  • Review

MeSH terms

  • Cell Cycle / genetics
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism
  • Cell Differentiation / genetics
  • Cell Transdifferentiation / genetics
  • Cell Transformation, Neoplastic / genetics
  • Cytokines / genetics
  • Cytokines / metabolism*
  • Guided Tissue Regeneration* / methods
  • Guided Tissue Regeneration* / trends
  • Humans
  • Inflammation
  • Interdisciplinary Communication
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / immunology
  • Mesenchymal Stem Cells / metabolism*
  • NF-kappa B / genetics
  • NF-kappa B / immunology
  • NF-kappa B / metabolism
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism
  • Neurodegenerative Diseases / genetics
  • Neurodegenerative Diseases / metabolism
  • Neurodegenerative Diseases / therapy*
  • Neurons / immunology
  • Neurons / metabolism*
  • Neurons / pathology
  • Poly-ADP-Ribose Binding Proteins
  • Repressor Proteins* / chemistry
  • Repressor Proteins* / genetics
  • Repressor Proteins* / metabolism
  • Ubiquitin-Protein Ligases

Substances

  • Cell Cycle Proteins
  • Cytokines
  • NF-kappa B
  • Neoplasm Proteins
  • Poly-ADP-Ribose Binding Proteins
  • RE1-silencing transcription factor
  • Repressor Proteins
  • CHFR protein, human
  • Ubiquitin-Protein Ligases