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Release of ciliary neurotrophic factor from cultured astrocytes and its modulation by cytokines

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Abstract

CNTF rescues various types of lesioned neurons in vivo, and it needs to be released from astrocytes into the extracellular space to have the effect. However, direct evidence for CNTF release has not been unequivocally demonstrated. We hypothesized that the rapid sequestration by CNTF receptor present on cultured astrocytes might be the cause of the inability to detect CNTF released into astrocyte-conditioned medium (ACM). Therefore, we measured CNTF immunoreactivity in medium conditioned by astrocytes treated with phosphatidylinositol-specific phospholipase C (PI-PLC) which was used to prevent released CNTF from binding to the CNTF receptor, since PI-PLC cleaves glycosyl-phosphatidylinositol anchor of CNTFRα, the unique component involved in CNTF binding. CNTF was not detectable in untreated ACM, but was detectable in PI-PLC-treated ACM. These results together with the evidence that PI-PLC treatment did not have a toxic effect on astrocytes prove the fact that CNTF can be released from astrocytes without cell lysis. Subsequently, the effect of cytokines such as IL-1β, TNF-α, and EGF on CNTF release was examined. These cytokines increased CNTF protein levels in ACMs without increasing CNTF protein levels in astrocyte-extracts, indicating that they enhanced CNTF release from astrocytes.

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References

  1. Adler, R., Landa, K., Manthorpe, M., and Varon, S. 1979. Cholinergic neuronotrophic factors: intraocular distribution of soluble trophic activity for ciliary neurons. Science 204:1434–1436.

    Google Scholar 

  2. Arakawa, Y., Sendtner, M., and Thoenen, H. 1990. Survival effect of ciliary neurotrophic factor (CNTF) on chick embryonic motoneurons in culture: comparison with other neurotrophic factors and cytokines. J. Neuroscl. 10:3507–3515.

    Google Scholar 

  3. Araujo, D.M., and Cotman, C.W. 1992. Basic FGF in astroglial, microglial, and neuronal cultures: characterization of binding sites and modulation of release by lymphokines and trophic factors. J. Neurosci. 12:1668–1678.

    Google Scholar 

  4. Asada, H., Ip, N.Y., Pan, L., Razack, N., Parfitt, M. M., and Plunkett, R.J. 1995. Time course of ciliary neurotrophic factor mRNA expression is coincident with the presence of protoplasmic astrocytes in traumatized rat striatum. J. Neurosci. Res. 40:22–30.

    Google Scholar 

  5. Davis, S., Aldrich, T.H., Ip, N.Y., Stahl, N., Scherer, S., Farruggella, T., DiStefano, P.S., Curtis, R., Panayotatos, N., Gascan, H., Chevalier, S., and Yancopoulos, G.D. 1993. Released form of CNTF receptor α component as a soluble mediator of CNTF responses. Science 259:1736–1739.

    Google Scholar 

  6. Davis, S., Aldrich, T.H., Stahl, N., Pan, L., Taga, T., Kishimoto, T., Ip, N.Y., and Yancopoulos, G.D. 1993. LIFRβ and gp130 as heterodimerizing signal transducers of the tripartite CNTF receptor. Science 260:1805–1808.

    Google Scholar 

  7. Davis, S., Aldrich, T.H., Valenzuela, D.M., Wong, V., Furth, M.E., Squinto, S.P., and Yancopoulos, G.D. 1991. The receptor for ciliary neurotrophic factor. Science 253:59–63.

    Google Scholar 

  8. Gearing, D.P., Thut, C.J., VandeBos, T., Gimpel, S.D., Delaney, P.B., King, J., Price, V., Cosman, D., and Beckmann, M.P. 1991. Leukemia inhibitory factor receptor is structurally related to the IL-6 signal transducer, gp130. EMBO J. 10:2839–2848.

    Google Scholar 

  9. Gradient, R.A., Cron, K.C., and Otten, U. 1990. Interleukin 1β and tumor necrosis factor α synergistically stimulate nerve growth factor (NGF) release from cultured rat astrocytes. Neurosci. Lett. 117:335–340.

    Google Scholar 

  10. Hagg, T., Quon, D., Higaki, J., and Varon, S. 1992. Ciliary neurotrophic factor prevents neuronal degeneration and promotes low affinity NGF receptor expression in the adult rat CNS. Neuron 8: 145–158.

    Google Scholar 

  11. Hagg, T., and Varon, S. 1993. Ciliary neurotrophic factor prevents degeneration of adult rat substantia nigra dopaminergic neurons in vivo. Proc. Natl. Acad. Sci. USA 90:6315–6319.

    Google Scholar 

  12. Heiter, E., Ayala, J., Bousseau, A., Denefle, P., and Prochiantz, A. 1990. Amoebiod microglial cells and not astrocytes synthesize TNF-α in Swiss mouse brain cell cultures. Eur. J. Neurosci. 2: 762–768.

    Google Scholar 

  13. Ip, N. Y., McClain, J., Barrezueta, N. X., Aldrich, T. H., Pan, L., Li, Y., Wiegand, S. J., Friedman, B., Davis, S., and Yancopoulos, G. D. 1993. The α component of the CNTF receptor is required for signaling and defines potential CNTF targets in the adult and during development. Neuron 10:89–102.

    Google Scholar 

  14. Ip, N. Y., Nye, S. H., Boulton, T. G., Davis, S., Taga, T., Li, Y., Birren, S. J., Yasukawa, K., Kishimoto, T., Anderson, D. J., Stahl, N., and Yancopoulos, G. D. 1992. CNTF and LIF act on neuronal cells via shared signaling pathways that involve the IL-6 signal transducing receptor component gp 130. Cell 69:1121–1132.

    Google Scholar 

  15. Ip, N. Y., Wiegand, S. J., Morse, J., and Rudge, J. S. 1993. Injuryinduced regulation of ciliary neurotrophic factor mRNA in the adult rat brain. Eur. J. Neurosci. 5:25–33.

    Google Scholar 

  16. Kessler, J. A., Ludlam, W. H., Freidin, M. M., Hall, D. H., Michaelson, M. D., Spray, D. C., Dougherty, M., and Batter, D. K. 1993. Cytokine-induced programmed death of cultured sympathetic neurons. Neuron 11:1123–1132.

    Google Scholar 

  17. Low, M. G., and Saltiel, A. R. 1988. Structural and functional roles of glycosyl-phosphatidylinositol in membranes. Science 239:268–275.

    Google Scholar 

  18. Marquardt, H., Hunkapiller, M. W., Hood, L. E., and Todaro, G. J. 1984. Rat transforming growth factor type 1: structure and relation to epidermal growth factor. Science 223:1079–1082.

    Google Scholar 

  19. Massague, J. 1983. Epidermal growth factor-like transforming growth factor. II. Interaction with epidermal growth factor receptors in human placenta membranes and A431 cells. J. Biol. Chem. 258:13614–13620.

    Google Scholar 

  20. Nieto-Sampedro, M., and Berman, M. A. 1987. Interleukin-1-like activity in rat brain: sources, targets, and effects of injury. J. Neurosci. Res. 17:214–219.

    Google Scholar 

  21. Richardson, P. M. 1994. Ciliary neurotrophic factor: a review. Pharmacol. Ther. 63:187–198.

    Google Scholar 

  22. Rudge, J. S., Alderson, R. F., Pasnikowski, E., McClain, J., Ip, N. Y., and Lindsay, R. M. 1992. Expression of ciliary neurotrophic factor and the neurotrophins-nerve growth factor, brainderived neurotrophic factor and neurotrophin-3-in cultured rat hippocampal astrocytes. Eur. J. Neurosci. 4:459–471.

    Google Scholar 

  23. Rudge, J. S., Li, Y., Pasnikowski, E. M., Mattsson, K., Pan, L., Yancopoulos, G. D., Wiegand, S. J., Lindsay, R. M., and Ip, N. Y. 1994. Neurotrophic factor receptors and their signal transduction capabilities in rat astrocytes. Eur. J. Neurosci. 6:693–705.

    Google Scholar 

  24. Rudge, J. S., Morrissey, D., Lindsay, R. M., and Pasnikowski, E. M. 1994. Regulation of ciliary neurotrophic factor in cultured rat hippocampal astrocytes. Eur. J. Neurosci. 6:218–229.

    Google Scholar 

  25. Saadat, S., Sendtner, M., and Rohrer, H. 1989. Ciliary neurotrophic factor induces cholinergic differentiation of rat sympathetic neurons in culture. J. Cell Biol. 108:1807–1816.

    Google Scholar 

  26. Sendtner, M., Kreutzberg, G. W., and Thoenen, H. 1990. Ciliary neurotrophic factor prevents the degeneration of motor neurons after axotomy. Nature 345:440–441.

    Google Scholar 

  27. Stockli, K. A., Lillien, L. E., Naher-Noe, M., Breitfeld, G., Hughes, R. A., Raff, M. C., Thoenen, H., and Sendtner, M., 1991. Regional distribution, developmental changes, and cellular localization of CNTF-mRNA and protein in the rat brain. J. Cell Biol. 115:447–459.

    Google Scholar 

  28. Stockli, K. A., Lottspeich, F., Sendtner, M., Masiakowski, P., Carroll, P., Gotz, R., Lindholm, D., and Thoenen, H. 1989. Molecular cloning, expression and regional distribution of rat ciliary neurotrophic factor. Nature 342:920–923.

    Google Scholar 

  29. Yoshida, K., and Gage, F. H., 1992. Cooperative regulation of nerve growth factor synthesis and secretion in fibroblasts and astrocytes by fibroblast growth factor and other cytokines. Brain Res. 569:14–25.

    Google Scholar 

  30. Yoshida, K., and Gage, F. H. 1991. Fibroblast growth factors stimulate nerve growth factor synthesis and secretion by astrocytes. Brain Res. 538:118–126.

    Google Scholar 

  31. Yoshida, K., Kakihana, M., Chen, L. S., Ong, M., Baird, A., and Gage, F. H. 1992. Cytokine regulation of nerve growth factormediated cholinergic neurotrophic activity synthesized by astrocytes and fibroblasts. J. Neurochem. 59:919–931.

    Google Scholar 

  32. Zurn, A. D., and Werren, F. 1994. Development of CNS cholinergic neurons in vitro: selective effects of CNTF and LIF on neurons from mesencephalic cranial motor nuclei. Dev. Biol. 163:309–315.

    Google Scholar 

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Kamiguchi, H., Yoshida, K., Sagoh, M. et al. Release of ciliary neurotrophic factor from cultured astrocytes and its modulation by cytokines. Neurochem Res 20, 1187–1193 (1995). https://doi.org/10.1007/BF00995382

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