Skip to main content

Change of Morphology and Cytoskeletal Protein Gene Expression during Dibutyryl cAMP-induced Differentiation in C6 Glioma Cells

Abstract

Elevation of the intracellular cAMP level induces morphological changes of astrocyte-like differentiation in C6 glioma cells. Such changes may be accompanied with expression of cytoskeletal protein genes. We therefore analyzed morphological changes after a treatment with dibutyryl cAMP (dbcAMP) and then assessed the expression of cytoskeletal protein genes by a quantitative real-time polymerase chain reaction. The cell number remained unaltered upon incubation with 1 mM dbcAMP in medium supplemented with 0.1% fetal bovine serum (FBS), whereas the number and lengths of processes increased, when compared with those of cells incubated in medium supplemented with 0.1% or 10% FBS only. The amounts of β-actin, γ-actin, and β-tubulin mRNAs in C6 cells, but not α-tubulin mRNA, increased during the early proliferation in DMEM containing 10% FBS. The expression of cytoskeletal protein genes decreased when incubated with 0.1% FBS or 1 mM dbcAMP in 0.1% FBS, compared with those of cells cultured in 10% FBS. These results indicated that, during the early proliferation in normal culture condition, the expression of cytoskeletal protein genes in C6 cells, except α-tubulin, increased, while in differentiating or differentiated C6 glioma cells, cAMP-induced morphological changes were not accompanied with elevation of gene expression for cytoskeletal proteins, such as actin and tubulin.

This is a preview of subscription content, access via your institution.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

References

  • Alberts B, Johnson A, Lewis J, Raff M, Roberts K, Walter P (2002) Molecular biology of the cell, 4th edn. Garland Science, New York

    Google Scholar 

  • Benda P, Lightbody J, Sato G, Levine L, Sweet W (1968) Differentiated rat glial cell strain in tissue culture. Science 161:370–371

    Article  CAS  PubMed  Google Scholar 

  • Chirgwin JM, Przybyla AE, MacDonald RJ, Rutter WJ (1979) Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry 18:5294–5299

    Article  CAS  PubMed  Google Scholar 

  • Cleveland DW (1989) Autoregulated control of tubulin synthesis in animal cells. Curr Opin Cell Biol 1:10–14

    Article  CAS  PubMed  Google Scholar 

  • Edlund T, Jessell TM (1999) Progression from extrinsic to intrinsic signaling in cell fate specification: a view from the nervous system. Cell 96:211–224

    Article  CAS  PubMed  Google Scholar 

  • Faivre-Sarrailh C, Ferraz C, Liautard JP, Rabie A (1990) Effect of thyroid deficiency on actin mRNA content in the developing rat cerebellum. Int J Dev Neurosci 8:99–106

    Article  CAS  PubMed  Google Scholar 

  • Goetschy JF, Ulrich G, Aunis D, Ciesielski-Treska J (1986) The organization and solubility properties of intermediate filaments and microtubules of cortical astrocytes in culture. J Neurocytol 15:375–387

    Article  CAS  PubMed  Google Scholar 

  • Goldman JE, Chiu FC (1984) Dibutyryl cyclic AMP causes intermediate filament accumulation and actin reorganization in astrocytes. Brain Res 306:85–95

    Article  CAS  PubMed  Google Scholar 

  • Knoops B, Octave JN (1997) Alpha 1-tubulin mRNA level is increased during neurite outgrowth of NG 108–15 cells but not during neurite outgrowth inhibition by CNS myelin. Neuroreport 10:795–798

    Article  Google Scholar 

  • Mizobuchi T, Yagi Y, Mizuno A (1990) Changes in alpha-tubulin and actin gene expression during optic nerve regeneration in frog retina. J Neurochem 55:54–59

    Article  CAS  PubMed  Google Scholar 

  • Otey CA, Kalnoski MH, Bulinski JC (1987) Identification and quantification of actin isoforms in vertebrate cells and tissues. J Cell Biochem 13:113–124

    Article  Google Scholar 

  • Paul S, Das S, Poddar R, Sarkar PK (1996) Role of thyroid hormone in the morphological differentiation and maturation of astrocytes: temporal correlation with synthesis and organization of actin. Eur J Neurosci 8:2361–2370

    Article  CAS  PubMed  Google Scholar 

  • Poddar R, Paul S, Chaudhury S, Sarkar PK (1996) Regulation of actin and tubulin gene expression by thyroid hormone during rat brain development. Brain Res Mol Brain Res 35:111–118

    Article  CAS  PubMed  Google Scholar 

  • Qian X, Shen Q, Goderie SK, He W, Capela A, Davis AA, Temple S (2000) Timing of CNS cell generation: a programmed sequence of neuron and glial cell production from isolated murine cortical stem cells. Neuron 28:69–80

    Article  CAS  PubMed  Google Scholar 

  • Sanger F, Nicklen S, Coulson AR (1977) DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci USA 74:5463–5467

    Article  CAS  PubMed  Google Scholar 

  • Sarkar S, Chaudhury S, Sarkar PK (1997) Regulation of beta- and gamma-actin mRNA by thyroid hormone in the developing rat brain. Neuroreport 8:1267–1271

    Article  CAS  PubMed  Google Scholar 

  • Sato S, Sugimura T, Yoda K, Fujimura S (1975) Morphological differentiation of cultured mouse glioblastoma cells induced by dibutyryl cyclic adenosine monophosphate. Cancer Res 35:2494–2499

    CAS  PubMed  Google Scholar 

  • Tabuchi K, Furuta T, Norikane H, Tsuboi M, Moriya Y, Nishimoto A (1981) Evaluation of the drug-induced morphological differentiation of rat glioma cells (C-6) from the aspects of S-100 protein level and con A binding pattern. J Neurol Sci 51:119–130

    Article  CAS  PubMed  Google Scholar 

  • Vallejo I, Vallejo M (2002) Pituitary adenylate cyclase-activating polypeptide induces astrocyte differentiation of precursor cells from developing cerebral cortex. Mol Cell Neurosci 21:671–683

    Article  CAS  PubMed  Google Scholar 

  • Wang W, Kimberly ED (1998) Quantitative analysis of mRNA expression of neuron-specific growth-associated genes in rat primary neurons by competitive RT-PCR. Brain Res Protoc 2:199–208

    Article  CAS  Google Scholar 

  • Willingham MC (1976) Cyclic AMP and cell behavior in cultured cells. Int Rev Cytol 44:319–363

    Article  CAS  PubMed  Google Scholar 

  • Yoshimura S, Sakai H, Nakashima S, Nozawa Y, Shinoda J, Sakai N, Yamada H (1997) Differential expression of Rho family GTP-binding proteins and protein kinase C isozymes during C6 glial cell differentiation. Brain Res Mol Brain Res 45:90–98

    Article  CAS  PubMed  Google Scholar 

  • Zimmer DB, Van Eldik LJ (1989) Analysis of the calcium-modulated proteins, S100 and calmodulin, and their target proteins during C6 glioma cell differentiation. J Cell Biol 108:141–151

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgment

The present study was partially supported by the 21st Century Center of Excellence Program for Advanced Life Science on the Base of Bioscience and Nanotechnology.

Author information

Affiliations

Authors

Corresponding author

Correspondence to Weiwei Hu.

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Hu, W., Onuma, T., Birukawa, N. et al. Change of Morphology and Cytoskeletal Protein Gene Expression during Dibutyryl cAMP-induced Differentiation in C6 Glioma Cells. Cell Mol Neurobiol 28, 519–528 (2008). https://doi.org/10.1007/s10571-007-9229-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10571-007-9229-y

Keywords

  • Actin
  • cAMP
  • Cytoskeleton
  • C6 glioma cell
  • Differentiation
  • Gene expression
  • Morphology
  • Tubulin