DOI QR코드

DOI QR Code

Characterization of Tunicamycin as Anti-obesity Agent

  • Song, Ha-Suk (Department of Life Sciences, University of Seoul) ;
  • Kim, Hye-Min (Department of Life Sciences, University of Seoul) ;
  • Jung, Sook-Yung (Department of Life Sciences, University of Seoul) ;
  • Lee, Dong-Hee (Department of Life Sciences, University of Seoul)
  • Published : 2009.04.30

Abstract

Adipocytes undergo adipocyte stress in the excessive presence of lipid. Adipocyte stress accompanies the typical signs of endoplasmic reticulum (ER) stress: unfolded protein response and overexpression of molecular chaperones. Apoptotic induction in adipocytes is known as a good strategy for treating obesity. The drug "tunicamycin" was tested for its therapeutic potential in inducing apoptosis on differentiating adipocytes of 3T3-L1. When the 3T3-L1 cells, stimulated for adipogenesis, were treated with tunicamycin, they showed typical ER stress symptoms. Despite progression in ER stress, however, the differentiated 3T3-L1 hardly proceeded to apoptosis based on the CHOP protein expression and FACS analysis. This is very different from C2C12, the myogenic counterpart of 3T3-L1, which showed significant apoptosis along with ER stress. This study also characterizes a potential mechanism whereby adipocyte may avoid apoptosis to sustain the pathological state of obesity. The level of GRP94 expression significantly upholds in 3T3-L1 under tunicamycin treatment compared to preadipocytes and C2C-12. When GRP94 expression was inhibited by siRNA, 3T3-L1 showed a higher level of CHOP expression compared to C2C12 cells. In conclusion, adipocytes exert an anti-apoptotic mechanism under ER stress caused by tunicamycin; thus, apoptotic induction in adipocyte is not a viable anti-obesity option. The unusual level of GRP94 may serve as a key role whereby adipocytes reach to the obesity level circumventing the apoptosis.

Keywords

References

  1. Aguari, P., Leo, S., Zavan, B., Vindigni, V., Rimessi, A., Bianchi, K., Franzin, C., Cortivo, R., Rossato, M., Vettor, R., Abatangelo, G., Pozzan, T., Pinton, P. and Rizzuto, R. (2007). High glucose induces adipogenic differentiation of musclederived stem cells. Proc. Natl. Acad. Sci. USA 105, 1227-1231
  2. Ahn, M. Y., Na, Y. J., Lee, J., Lee, B. M. and Kim, H. S. (2009). Apicidin induces ipoptosis via Cytochrome c-mediated intrinsic pathway in human ovarian cancer cells. Biomol. Ther. 17, 17-24 https://doi.org/10.4062/biomolther.2009.17.1.17
  3. Fu, M., Sun, T., Bookout, A. L., Downes, M., Yu, R. T., Evans R. M. and Mangelsdorf, D. J. (2005). A nuclear receptor atlas: 3T3-L1 adipogenesis. Mol. Endocrinol. 19, 2437-2450 https://doi.org/10.1210/me.2004-0539
  4. Jiang, C. C., Chen, L.H., Gillespie, S., Kiejda, K.A., Mhaidat, N., Wang, Y. F., Thorne, R., Zhang, X. D. and Hersey, P. (2007). Tunicamycin sensitizes human melanoma cells to tumor necrosis factor-related apoptosis-inducing ligand-induced apoptosis by up-regulation of TRAIL-R2 via the unfolded protein response. Cancer Res. 67, 5880-5888 https://doi.org/10.1158/0008-5472.CAN-07-0213
  5. Lane, M. D. and Tang, Q. Q. (2005). From multipotent stem cell to adipocyte. Clinical & Molecular Thera. 73, 476
  6. Lee, A. S. (2001). The glucose-regulated proteins: stress induction and clinical applications. Trends Biochem. Sci. 26, 504 https://doi.org/10.1016/S0968-0004(01)01908-9
  7. Lee, S. Y. and Kim, D. H. (2004). Inhibition of Apoptosis is responsible for the acquired resistance of K562 cells to Cisplatin. Biomol. Ther. 12, 85-91
  8. Li, J., Lee, B. and Lee, A. S. (2006). Endoplasmic reticulum stress-induced apoptosis. J. Biol. Chem. 281, 7260 https://doi.org/10.1074/jbc.M509868200
  9. Nakanishi, K., Sudo, T. and Morishima, N. (2005). Endoplasmic reticulum stress signaling transmitted by ATF6 mediates apoptosis during muscle development. J. Cell Biol. 106, 555 https://doi.org/10.1083/jcb.200412024
  10. Nawrocki, A. R. and Scherer, P. E. (2005). The adipocyte as a drug discovery target. Drug Disc. Today 10, 1219-1230 https://doi.org/10.1016/S1359-6446(05)03569-5
  11. Ni, M. and Lee, A. S. (2007). ER chaperones in mammalian development and human diseases. FEBS Lett. 581, 3641 https://doi.org/10.1016/j.febslet.2007.04.045
  12. Oyadomari, S., Yun, C., Fisher, E. A., Kreglinger, N., Kreibich, G., Oyadomari, M., Harding, H. P., Goodman, A. G., Harant, H., Garrison, J. L., Taunton, J., Katze, M. G. and Ron, D. (2006). Cotranslocational degradation protects the stressed endoplasmic reticulum from protein overload. Cell 126, 727-739 https://doi.org/10.1016/j.cell.2006.06.051
  13. Ozcan, U., Cao, Q, Erkan, Y., Lee, A., Glimcher, H. and Hotamisligil, G. S. (2004). Endoplasmic reticulum stress links obesity insulin action type 2 diabetes. Science 306, 457-461 https://doi.org/10.1126/science.1103160
  14. Puthalakath, H. A., O'Reilly, L., Gunn, P., Lee, L. N., Kelly, P. D., Huntington, N. D., Hughes, P. M. and Michalak, E. (2007). ER Stress triggers apoptosis by activating BH3-Only protein Bim. Cell 129, 1337 https://doi.org/10.1016/j.cell.2007.04.027
  15. Ron, D. and Walter, P. (2007). Signal integration in the endoplasmic reticulum unfolded response. Nat. Rev. Mol. Cell. Biol. 8, 519-529 https://doi.org/10.1038/nrm2199
  16. Rutkowski, D. T., Wu, J., Back, S. H., Callaghan, M. U., Ferris, S. P., Iqbal, J., Clark, R., Miao, H., Hassler, J. R., Fornek, J., Katze, M. G., Hussain, M. M., Song, B., Swathirajan, J., Wang, J., Yau, G. D. Y. and Kaufman, R. J. (2008). UPR pathways combine to prevent hepatic steatosis caused by ER stress-mediated suppression of transcriptional master regulators. Dev. Cell 15, 829-840 https://doi.org/10.1016/j.devcel.2008.10.015
  17. Sheu, M. L., Liu, S. H. and Lan, K. H. (2007). Honokiol induces Calpain-mediated glucose-regulated protein-94 cleavage and apoptosis in human gastric cancer cells and reduces tumor growth. PLoSone 10, e1096 https://doi.org/10.1371/journal.pone.0001096
  18. Shimoke, K., Kishi, S., Utsumi, T., Shimamura, Y., Sasaya, H., Oikawa, T., Uesato, S. and Ikeuchi, T. (2005). NGF-induced phosphatidylinositol 3-kinase signaling pathway prevents thapsigargin-triggered ER stress-mediated apoptosis in PC12 cells. Neurosci. Lett. 389, 124-128 https://doi.org/10.1016/j.neulet.2005.07.030
  19. Zinszner, H., Kuroda, M., Wang X. Z. and Batchvarova, N. (2007). CHOP is implicated in programmed cell death in response to impaired function of the endoplasmic reticulum. Genes Dev. 12, 982 https://doi.org/10.1101/gad.12.7.982

Cited by

  1. KIOM-79 attenuated cell damage induced by endoplasmic reticulum stress by inhibiting apoptosis in RINm5F cells vol.16, pp.6, 2011, https://doi.org/10.1007/s12257-011-0120-9
  2. Mitogen activated protein kinases are prime signalling enzymes in nitric oxide production induced by soluble β-glucan from Sparassis crispa vol.33, pp.11, 2010, https://doi.org/10.1007/s12272-010-1107-3
  3. 20-O-(β-D-glucopyranosyl)-20(S)-protopanaxadiol induces apoptosis via induction of endoplasmic reticulum stress in human colon cancer cells vol.29, pp.4, 2013, https://doi.org/10.3892/or.2013.2270
  4. Wen-pi-tang-Hab-Wu-ling-san, a Polyherbal Medicine, Attenuates ER Stress in 3T3-L1 Preadipocytes by Promoting the Insulin Signaling Pathway vol.2013, 2013, https://doi.org/10.1155/2013/825814