Skip to main content

Measuring GSK3 Expression and Activity in Cells

  • Protocol
Wnt Signaling

Part of the book series: Methods in Molecular Biology™ ((MIMB,volume 468))

Abstract

Glycogen synthase kinase (GSK)-3 is a key signalling intermediate in the action of Wnts. This protein kinase is ubiquitously expressed and has high inherent activity but is inhibited by activation of Wnt signalling or activation of growth factor receptor tyrosine kinases (e.g. insulin, nerve growth factor [NGF], platelet-derived growth factor [PDGF], etc.). The degree of inhibition of GSK3 in cells treated with such reagents is dependent on the cell type and the stimulus used. Therefore, the ability to accurately measure GSK3 activity in cells is an important aspect of GSK3 research. The activity of GSK3 is reduced by posttranslational modi fication (phosphorylation) and this can be measured by immunoblot with specific reagents (indirect), or by immunoprecipitation and assay (direct), as long as the modification is protected during these procedures. However, inhibition by phosphorylation is specific to cellular activation by growth factors and nutrients. Wnt inhibition of GSK3 does not involve phosphorylation of these residues on GSK3 and therefore it can not be measured using this modification. Currently, the simplest way to assess Wnt inhibition of GSK3 is to monitor phosphorylation of specific GSK3 substrates in cells (e.g. β-catenin). Alternatively, Wnt inhibition of GSK3 can be measured by partial purification of cellular GSK3 by ion exchange chromatography and assay of fractions or possibly by immunoprecipitation and assay. In this chapter, we demonstrate the use of the different approaches to measure GSK3 activity in SH-SY5Y cells, describe the best antibodies currently available, and discuss the potential drawbacks of each method.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Protocol
USD 49.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 84.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 109.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. Woodgett, J. R. (1990) Molecular cloning and expression of glycogen synthase kinase-3/factor A. EMBO J. 9, 2431–2438.

    CAS  PubMed  Google Scholar 

  2. Hansen, L., Arden, K. C., Rasmussen, S. B., Viars, C. S., Vestergaard, H., Hansen, T., et al. (1997) Chromosomal mapping and mutational analysis of the coding region of the glycogen synthase kinase-3alpha and beta isoforms in patients with NIDDM. Diabetologia 40, 940–946.

    Article  CAS  PubMed  Google Scholar 

  3. Shaw, P. C., Davies, A. F., Lau, K. F., Garcia-Barcelo, M., Waye, M. M., Lovestone, S., et al. (1998) Isolation and chromosomal mapping of human glycogen synthase kinase-3 alpha and -3 beta encoding genes. Genome 41, 720–727.

    Article  CAS  PubMed  Google Scholar 

  4. Mukai, F., Ishiguro, K., Sano, Y., and Fujita, S. C. (2002) Alternative splicing isoform of tau protein kinase I/glycogen synthase kinase 3beta. J. Neurochem. 81, 1073–1083.

    Article  CAS  PubMed  Google Scholar 

  5. Embi, N., Rylatt, D. B., and Cohen, P. (1980) Glycogen synthase kinase-3 from rabbit skeletal muscle. Separation from cyclic-AMP-dependent protein kinase and phosphorylase kinase. Eur. J. Biochem. 107, 519–527.

    Article  CAS  PubMed  Google Scholar 

  6. Cohen, P. and Goedert, M. (2004) GSK3 inhibitors: development and therapeutic potential. Nat. Rev. Drug Discov. 3, 479–487.

    Article  CAS  PubMed  Google Scholar 

  7. Frame, S. and Cohen, P. (2001) GSK3 takes centre stage more than 20 years after its discovery. Biochem. J. 359, 1–16.

    Article  CAS  PubMed  Google Scholar 

  8. Frame, S., Cohen, P., and Biondi, R. M. (2001) A common phosphate binding site explains the unique substrate specificity of GSK3 and its inactivation by phosphoryla tion. Mol. Cell 7, 1321–1327.

    Article  CAS  PubMed  Google Scholar 

  9. Thomas, G. M., Frame, S., Goedert, M., Nathke, I., Polakis, P., and Cohen, P. (1999) A GSK3-binding peptide from FRAT1 selectively inhibits the GSK3-cata-lysed phosphorylation of axin and beta-cat enin. FEBS Lett. 458, 247–251.

    Article  CAS  PubMed  Google Scholar 

  10. Ding, V. W., Chen, R. H., and McCormick, F. (2000) Differential regulation of glyco gen synthase kinase 3beta by insulin and Wnt signaling. J. Biol. Chem. 275, 32475– 32481.

    Article  CAS  PubMed  Google Scholar 

  11. Liu, X., Rubin, J. S., and Kimmel, A. R. (2005) Rapid, Wnt-induced changes in GSK3beta associations that regulate beta catenin stabilization are mediated by Gal pha proteins. Curr. Biol. 15, 1989–1997.

    Article  CAS  PubMed  Google Scholar 

  12. Cook, D., Fry, M. J., Hughes, K., Sumath ipala, R., Woodgett, J. R., and Dale, T. C. (1996) Wingless inactivates glycogen syn thase kinase-3 via an intracellular signalling pathway which involves a protein kinase C. EMBO J. 15, 4526–4536.

    CAS  PubMed  Google Scholar 

  13. Sutherland, C., Leighton, I. A., and Cohen, P. (1993) Inactivation of glycogen synthase kinase-3 beta by phosphorylation: new kinase connections in insulin and growth-factor signalling. Biochem. J. 296 (Pt 1), 15–19.

    CAS  PubMed  Google Scholar 

  14. Cole, A., Frame, S., and Cohen, P. (2004) Further evidence that the tyrosine phosphor-ylation of glycogen synthase kinase-3 (GSK3) in mammalian cells is an autophosphoryla tion event. Biochem. J. 377, 249–255.

    Article  CAS  PubMed  Google Scholar 

  15. Cole, A. R., Knebel, A., Morrice, N. A., Robertson, L. A., Irving, A. J., Connolly, C. N. et al. (2004) GSK-3 phosphoryla tion of the Alzheimer epitope within col lapsin response mediator proteins regulates axon elongation in primary neurons. J. Biol. Chem. 279, 50176–50180.

    Article  CAS  PubMed  Google Scholar 

  16. Hart, M. J., de los, S. R., Albert, I. N., Rubinfeld, B., and Polakis, P. (1998) Downregulation of beta-catenin by human Axin and its association with the APC tumor suppressor, beta-catenin and GSK3 beta. Curr. Biol. 8, 573–581.

    Article  CAS  PubMed  Google Scholar 

  17. Itoh, K., Krupnik, V. E., and Sokol, S. Y. (1998) Axis determination in Xenopus involves biochemical interactions of axin, glycogen synthase kinase 3 and beta-cat enin. Curr. Biol. 8, 591–594.

    Article  CAS  PubMed  Google Scholar 

  18. Laemmli, U. K. (1970) Cleavage of struc tural proteins during the assembly of the head of bacteriophage T4. Nature 227, 680–685.

    Article  CAS  PubMed  Google Scholar 

  19. Bradford, M. M. (1976) A rapid and sensi tive method for the quantitation of micro-gram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72, 248–254.

    Article  CAS  PubMed  Google Scholar 

  20. Cross, D. A., Culbert, A. A., Chalmers, K. A., Facci, L., Skaper, S. D., and Reith, A. D. (2001) Selective small-molecule inhibitors of glycogen synthase kinase-3 activity protect primary neurones from death. J. Neurochem. 77, 94–102.

    Article  CAS  PubMed  Google Scholar 

  21. Cross, D. A., Alessi, D. R., Vandenheede, J. R., McDowell, H. E., Hundal, H. S., and Cohen, P. (1994) The inhibi tion of glycogen synthase kinase-3 by insulin or insulin-like growth factor 1 in the rat skeletal muscle cell line L6 is blocked by wortmannin, but not by rapamycin: evidence that wortmannin blocks activation of the mitogen-acti vated protein kinase pathway in L6 cells between Ras and Raf. Biochem. J. 303 (Pt 1), 21–26.

    CAS  PubMed  Google Scholar 

Download references

Acknowledgments

This work was supported by the Alzheimer's Research Trust and Diabetes UK.

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2008 Humana Press, a part of Springer Science+Business Media, LLC

About this protocol

Cite this protocol

Cole, A.R., Sutherland, C. (2008). Measuring GSK3 Expression and Activity in Cells. In: Vincan, E. (eds) Wnt Signaling. Methods in Molecular Biology™, vol 468. Humana Press. https://doi.org/10.1007/978-1-59745-249-6_4

Download citation

  • DOI: https://doi.org/10.1007/978-1-59745-249-6_4

  • Publisher Name: Humana Press

  • Print ISBN: 978-1-58829-912-3

  • Online ISBN: 978-1-59745-249-6

  • eBook Packages: Springer Protocols

Publish with us

Policies and ethics