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Trans-differentiation via Epigenetics: A New Paradigm in the Bone Regeneration

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초록

In regenerative medicine, growing cells or tissues in the laboratory is necessary when damaged cells can not heal by themselves. Acquisition of the required cells from the patient’s own cells or tissues is an ideal option without additive side effects. In this context, cell reprogramming methods, including the use of induced pluripotent stem cells (iPSCs) and trans-differentiation, have been widely studied in regenerative research. Both approaches have advantages and disadvantages, and the possibility of de-differentiation because of the epigenetic memory of iPSCs has strengthened the need for controlling the epigenetic background for successful cell reprogramming. Therefore, interest in epigenetics has increased in the field of regenerative medicine. Herein, we outline in detail the cell trans-differentiation method using epigenetic modification for bone regeneration in comparison to the use of iPSCs.

Abstract

In regenerative medicine, growing cells or tissues in the laboratory is necessary when damaged cells can not heal by themselves. Acquisition of the required cells from the patient’s own cells or tissues is an ideal option without additive side effects. In this context, cell reprogramming methods, including the use of induced pluripotent stem cells (iPSCs) and trans-differentiation, have been widely studied in regenerative research. Both approaches have advantages and disadvantages, and the possibility of de-differentiation because of the epigenetic memory of iPSCs has strengthened the need for controlling the epigenetic background for successful cell reprogramming. Therefore, interest in epigenetics has increased in the field of regenerative medicine. Herein, we outline in detail the cell trans-differentiation method using epigenetic modification for bone regeneration in comparison to the use of iPSCs.

참고문헌 (31)

  1. Dimitriou R, "Bone regeneration: current concepts and future directions", BMC Med, 9, pp.66~ (2011)[DOI]
  2. Henkel J, "Bone regeneration based on tissue engineering conceptions: a 21st century perspective", Bone Res, 1, pp.216~248 (2013)[DOI]
  3. Robinton DA, "The promise of induced pluripotent stem cells in research and therapy", Nature, 481, pp.295~305 (2012)[DOI]
  4. Feil R, "Epigenetics and the environment: emerging patterns and implications", Nat Rev Genet, 13, pp.97~109 (2012)[DOI]
  5. Dupont C, "Epigenetics: definition, mechanisms and clinical perspective", Semin Reprod Med, 27, pp.351~357 (2009)[DOI]
  6. Cho YD, "Epigenetic modifications and canonical wingless", int-1 class (WNT) signaling enable trans-differentiation of nonosteogenic cells into osteoblasts, 2014, pp.289, 20120~20128
  7. Mondal T, "Characterization of the RNA content of chromatin", Genome Res, 20, pp.899~907 (2010)[DOI]
  8. Gardiner-Garden M, "CpG islands in vertebrate genomes", J Mol Biol, 196, pp.261~282 (1987)[DOI]
  9. Kafri T, "Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line", Genes Dev, 6, pp.705~714 (1992)[DOI]
  10. Bestor T, "Cloning and sequencing of a cDNA encoding DNA methyltransferase of mouse cells. The carboxyl-terminal domain of the mammalian enzymes is related to bacterial restriction methyltransferases", J Mol Biol, 203, pp.971~983 (1988)[DOI]
  11. Bannister AJ, "Regulation of chromatin by histone modifications", Cell Res, 21, pp.381~395 (2011)[DOI]
  12. Shiota K, "DNA methylation profiles of CpG islands for cellular differentiation and development in mammals", Cytogenet Genome Res, 105, pp.325~334 (2004)[DOI]
  13. Ohgane J, "Epigenetics: the DNA methylation profile of tissue-dependent and differentially methylated regions in cells", Placenta, 29(Suppl A), pp.S29~S35 (2008)[DOI]
  14. Takahashi K, "Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors", Cell, 126, pp.663~676 (2006)[DOI]
  15. Medvedev SP, "Induced pluripotent stem cells: problems and advantages when applying them in regenerative medicine", Acta Naturae, 2, pp.18~28.a (2010)
  16. Duan X, "Application of induced pluripotent stem (iPS) cells in periodontal tissue regeneration", J Cell Physiol, 226, pp.150~157 (2011)[DOI]
  17. Hynes K, "Induced pluripotent stem cells: a new frontier for stem cells in dentistry", J Dent Res, 94, pp.1508~1515 (2015)[DOI]
  18. Selman K, "Transdifferentiation in the labial gland of silk moths: is DNA required for cellular metamorphosis?", Cell Differ, 3, pp.81~94 (1974)[DOI]
  19. Eguchi G, "Differentiation of lens tissue from the progeny of chick retinal pigment cells cultured in vitro: a demonstration of a switch of cell types in clonal cell culture", Proc Natl Acad Sci U S A, 70, pp.1495~1499 (1973)[DOI]
  20. Xu J, "Direct lineage reprogramming: strategies, mechanisms, and applications", Cell Stem Cell, 16, pp.119~134 (2015)[DOI]
  21. Cho YD, "Epigenetic priming confers direct cell trans-differentiation from adipocyte to osteoblast in a transgene-free state", J Cell Physiol, 231, pp.1484~1494 (2016)[DOI]
  22. Cho Y, "Direct gingival fibroblast", osteoblast transdifferentiation via epigenetics, 2017, pp.96, 555~561
  23. Waddington CH, "The strategy of the genes: A discussion of some aspects of theoretical biology" (1957), Allen & Unwin
  24. Cho YD, "Wnt3a stimulates Mepe, matrix extracellular phosphoglycoprotein, expression directly by the activation of the canonical Wnt signaling pathway and indirectly through the stimulation of autocrine Bmp-2 expression", J Cell Physiol, 227, pp.2287~2296 (2012)[DOI]
  25. Graf T, "Forcing cells to change lineages", Nature, 462, pp.587~594 (2009)[DOI]
  26. Jopling C, "Dedifferentiation, transdifferentiation and reprogramming: three routes to regeneration", Nat Rev Mol Cell Biol, 12, pp.79~89 (2011)[DOI]
  27. Xie H, "Stepwise reprogramming of B cells into macrophages", Cell, 117, pp.663~676 (2004)[DOI]
  28. Meivar-Levy I, "Pancreatic and duodenal homeobox gene 1 induces hepatic dedifferentiation by suppressing the expression of CCAAT", enhancerbinding protein beta, 2007, pp.46, 898~905
  29. Ieda M, "Direct reprogramming of fibroblasts into functional cardiomyocytes by defined factors", Cell, 142, pp.375~386 (2010)[DOI]
  30. Garg V, "GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5", Nature, 424, pp.443~447 (2003)[DOI]
  31. Lin Q, "Control of mouse cardiac morphogenesis and myogenesis by transcription factor MEF2C", Science, 276, pp.1404~1407 (1997)[DOI]

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