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2011 | 16 | 1 |

Tytuł artykułu

Differential redox potential profiles during adipogenesis and osteogenesis

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Development is an orderly process that requires the timely activation and/or deactivation of specific regulatory elements that control cellular proliferation, differentiation and apoptosis. While many studies have defined factors that control developmental signaling, the role of intracellular reduction/oxidation (redox) status as a means to control differentiation has not been fully studied. Redox states of intracellular couples may play a very important role in regulating redox-sensitive elements that are involved in differentiation signaling into specific phenotypes. In human mesenchymal stem cells (hMSCs), which are capable of differentiating into many different types of phenotypes, including osteoblasts and adipocytes, glutathione (GSH), cysteine (Cys) and thioredoxin-1 (Trx1) redox potentials were measured during adipogenesis and osteogenesis. GSH redox potentials (Eh) during both osteogenesis and adipogenesis became increasingly oxidized as differentiation ensued, but the rate at which this oxidation occurred was unique for each process. During adipogenesis, Cys Eh became oxidized as adipogenesis progressed but during osteogenesis, it became reduced. Interestingly, intracellular Trx1 concentrations appeared to increase in both adipogenesis and osteogenesis, but the Eh was unchanged when compared to undifferentiated hMSCs. These data show that hMSC differentiation into either adipocytes of osteoblasts corresponds to a unique redox state profile, suggesting that differentiation into specific phenotypes are likely regulated by redox states that are permissive to a specific developmental process.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

16

Numer

1

Opis fizyczny

p.149-161,fig.,ref.

Twórcy

autor
  • Division of Pulmonary, Allergy/Immunology, Cystic Fibrosis and Sleep, Department of Pediatrics, Emory School of Medicine, Emory University Atlanta, 2015 Uppergate Drive Suite 350, Altanta, GA 30322, USA
autor

Bibliografia

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  • 10. Jiang, S., Moriarty, S.E., Grossniklaus, H., Nelson, K.C., Jones, D.P. and Sternberg, P. Jr. Increased oxidant-induced apoptosis in cultured nondividing human retinal pigment epithelial cells. Invest. Ophthalmol. Vis. Sci. 43 (2002) 2546-2553.
  • 11. Watson, W.H., Pohl, J., Montfort, W.R., Stuchlik, O., Reed, M.S., Powis, G. and Jones, D.P. Redox potential of human thioredoxin 1 and identification of a second dithiol/disulfide motif. J. Biol. Chem. 278 (2003) 33408-33415.
  • 12. Gregory, C.A., Perry, A.S., Reyes, E., Conley, A., Gunn, W.G. and Prockop, D.J. Dkk-1-derived synthetic peptides and lithium chloride for the control and recovery of adult stem cells from bone marrow. J. Biol. Chem. 280 (2005) 2309-2323.
  • 13. Sekiya, I., Larson, B.L., Smith, J.R., Pochampally, R., Cui, J.G. and Prockop, D.J. Expansion of human adult stem cells from bone marrow stroma: conditions that maximize the yields of early progenitors and evaluate their quality. Stem Cells 20 (2002) 530-541.
  • 14. Sekiya, I., Larson, B.L., Vuoristo, J.T., Cui, J.G. and Prockop, D.J. Adipogenic differentiation of human adult stem cells from bone marrow stroma (MSCs). J. Bone Miner. Res. 19 (2004) 256-264.
  • 15. Hansen, J.M., Zhang, H. and Jones, D.P. Differential oxidation of thioredoxin-1, thioredoxin-2, and glutathione by metal ions. Free Radic. Biol. Med. 40 (2006) 138-145.
  • 16. Halvey, P.J., Watson, W.H., Hansen, J.M., Go, Y.M., Samali, A. and Jones, D.P. Compartmental oxidation of thiol-disulphide redox couples during epidermal growth factor signalling. Biochem. J. 386 (2005) 215-219.
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  • 22. Matthews, J.R., Wakasugi, N., Virelizier, J.L., Yodoi, J. and Hay, R.T. Thioredoxin regulates the DNA binding activity of NF-kappa B by reduction of a disulphide bond involving cysteine 62. Nucleic Acids Res. 20 (1992) 3821-3830.
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Bibliografia

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