Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1983 Jul 1;97(1):92–98. doi: 10.1083/jcb.97.1.92

Ionic responses and growth stimulation induced by nerve growth factor and epidermal growth factor in rat pheochromocytoma (PC12) cells

PMCID: PMC2112476  PMID: 6306015

Abstract

Rat pheochromocytoma cells (clone PC12) respond to nerve growth factor (NGF) by the acquirement of a phenotype resembling neuronal cells. In an earlier study we showed that NGF causes an increase in Na+,K+ pump activity, as monitored by ouabain-sensitive Rb+ influx. Here we show that addition of epidermal growth factor (EGF) to PC12 cells resulted in a stimulation of Na+,K+ pump activity as well. The increase of Na+,K+ pump activity by NGF or EGF was due to increased Na+ influx. This increased Na+ influx was sensitive to amiloride, an inhibitor of Na+,H+ exchange. Furthermore, no changes in membrane potential were observed upon addition of NGF or EGF. Amiloride-sensitive Na+,H+ exchange in PC12 cells was demonstrated by H+ efflux measurements and the effects of weak acids on Na+ influx. These observations suggest that both NGF and EGF activate an amiloride-sensitive, electroneutral Na+,H+ exchange mechanism in PC12 cells. These findings were surprising in view of the opposite ultimate biological effects of NGF and EGF, e.g., growth arrest vs. growth stimulation. However, within 24 h after addition, NGF was found to stimulate growth of PC12 cells, comparable to EGF. In the presence of amiloride, this stimulated growth by NGF and EGF was abolished. In contrast, amiloride did not affect NGF-induced neurite outgrowth of PC12 cells. From these observations it is concluded that in PC12 cells: (a) NGF has an initial growth stimulating effect; (b) neurite outgrowth is independent of increased amiloride- sensitive Na+ influx; and (c) growth stimulation by NGF and EGF is associated with increased amiloride-sensitive Na+ influx.

Full Text

The Full Text of this article is available as a PDF (1.2 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Adler R., Manthorpe M., Skaper S. D., Varon S. Polyornithine-attached neurite-promoting factors (PNPFs). Culture sources and responsive neurons. Brain Res. 1981 Feb 9;206(1):129–144. doi: 10.1016/0006-8993(81)90105-0. [DOI] [PubMed] [Google Scholar]
  2. Boonstra J., Mummery C. L., Tertoolen L. G., Van Der Saag P. T., De Laat S. W. Cation transport and growth regulation in neuroblastoma cells. Modulations of K+ transport and electrical membrane properties during the cell cycle. J Cell Physiol. 1981 Apr;107(1):75–83. doi: 10.1002/jcp.1041070110. [DOI] [PubMed] [Google Scholar]
  3. Boonstra J., Skaper S. D., Varon S. Regulation of Na+,K+ pump activity by nerve growth factor in chick embryo dorsal root ganglion cells. J Cell Physiol. 1982 Oct;113(1):28–34. doi: 10.1002/jcp.1041130107. [DOI] [PubMed] [Google Scholar]
  4. Boonstra J., van der Saag P. T., Moolenaar W. H., de Laat S. W. Rapid effects of nerve growth factor on the Na+, K+-pump in rat pheochromocytoma cells. Exp Cell Res. 1981 Feb;131(2):452–455. doi: 10.1016/0014-4827(81)90255-x. [DOI] [PubMed] [Google Scholar]
  5. Chandler C. E., Herschman H. R. Tumor promoter modulation of epidermal growth factor- and nerve growth factor-induced adhesion and growth factor binding of PC-12 pheochromocytoma cells. J Cell Physiol. 1980 Nov;105(2):275–285. doi: 10.1002/jcp.1041050211. [DOI] [PubMed] [Google Scholar]
  6. Davidson R. L., O'Malley K. A., Wheeler T. B. Polyethylene glycol-induced mammalian cell hybridization: effect of polyethylene glycol molecular weight and concentration. Somatic Cell Genet. 1976 May;2(3):271–280. doi: 10.1007/BF01538965. [DOI] [PubMed] [Google Scholar]
  7. Dichter M. A., Tischler A. S., Greene L. A. Nerve growth factor-induced increase in electrical excitability and acetylcholine sensitivity of a rat pheochromocytoma cell line. Nature. 1977 Aug 11;268(5620):501–504. doi: 10.1038/268501a0. [DOI] [PubMed] [Google Scholar]
  8. End D., Tolson N., Yu M. Y., Guroff G. Effects of 12-0-Tetradecanoylphorbol-13-acetate (TPA) on rat pheochromocytoma (PC12) cells: interactions with epidermal growth factor and nerve growth factor. J Cell Physiol. 1982 May;111(2):140–148. doi: 10.1002/jcp.1041110204. [DOI] [PubMed] [Google Scholar]
  9. Fehlmann M., Canivet B., Freychet P. Epidermal growth factor stimulates monovalent cation transport in isolated rat hepatocytes. Biochem Biophys Res Commun. 1981 May 15;100(1):254–260. doi: 10.1016/s0006-291x(81)80090-3. [DOI] [PubMed] [Google Scholar]
  10. Goodman R., Herschman H. R. Growth factor dependence of pheochromocytoma cells in chemically defined medium. J Neurosci Res. 1982;7(4):453–459. doi: 10.1002/jnr.490070412. [DOI] [PubMed] [Google Scholar]
  11. Goodman R., Slater E., Herschman H. R. Epidermal growth factor induces tyrosine hydroxylase in a clonal pheochromocytoma cell line, PC-G2. J Cell Biol. 1980 Mar;84(3):495–500. doi: 10.1083/jcb.84.3.495. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Greene L. A., Tischler A. S. Establishment of a noradrenergic clonal line of rat adrenal pheochromocytoma cells which respond to nerve growth factor. Proc Natl Acad Sci U S A. 1976 Jul;73(7):2424–2428. doi: 10.1073/pnas.73.7.2424. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Gunning P. W., Landreth G. E., Bothwell M. A., Shooter E. M. Differential and synergistic actions of nerve growth factor and cyclic AMP in PC12 cells. J Cell Biol. 1981 May;89(2):240–245. doi: 10.1083/jcb.89.2.240. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Gunning P. W., Letourneau P. C., Landreth G. E., Shooter E. M. The action of nerve growth factor and dibutyryl adenosine cyclic 3':5'-monophosphate on rat pheochromocytoma reveals distinct stages in the mechanisms underlying neurite outgrowth. J Neurosci. 1981 Oct;1(10):1085–1095. doi: 10.1523/JNEUROSCI.01-10-01085.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Guroff G., Dickens G., End D. The induction of ornithine decarboxylase by nerve growth factor and epidermal growth factor in PC12 cells. J Neurochem. 1981 Aug;37(2):342–349. doi: 10.1111/j.1471-4159.1981.tb00461.x. [DOI] [PubMed] [Google Scholar]
  16. Halegoua S., Patrick J. Nerve growth factor mediates phosphorylation of specific proteins. Cell. 1980 Nov;22(2 Pt 2):571–581. doi: 10.1016/0092-8674(80)90367-0. [DOI] [PubMed] [Google Scholar]
  17. Herrup K., Thoenen H. Properties of the nerve growth factor receptor of a clonal line of rat pheochromocytoma (PC12) cells. Exp Cell Res. 1979 Jun;121(1):71–78. doi: 10.1016/0014-4827(79)90445-2. [DOI] [PubMed] [Google Scholar]
  18. Heumann R., Schwab M., Thoenen H. A second messenger required for nerve growth factor biological activity? Nature. 1981 Aug 27;292(5826):838–840. doi: 10.1038/292838a0. [DOI] [PubMed] [Google Scholar]
  19. Huff K. R., Guroff G. Nerve growth factor-induced reduction in epidermal growth factor responsiveness and epidermal growth factor receptors in PC12 cells: an aspect of cell differentiation. Biochem Biophys Res Commun. 1979 Jul 12;89(1):175–180. doi: 10.1016/0006-291x(79)90960-4. [DOI] [PubMed] [Google Scholar]
  20. Huff K., End D., Guroff G. Nerve growth factor-induced alteration in the response of PC12 pheochromocytoma cells to epidermal growth factor. J Cell Biol. 1981 Jan;88(1):189–198. doi: 10.1083/jcb.88.1.189. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Koch K. S., Leffert H. L. Increased sodium ion influx is necessary to initiate rat hepatocyte proliferation. Cell. 1979 Sep;18(1):153–163. doi: 10.1016/0092-8674(79)90364-7. [DOI] [PubMed] [Google Scholar]
  22. Lander A. D., Fujii D. K., Gospodarowicz D., Reichardt L. F. Characterization of a factor that promotes neurite outgrowth: evidence linking activity to a heparan sulfate proteoglycan. J Cell Biol. 1982 Sep;94(3):574–585. doi: 10.1083/jcb.94.3.574. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Landreth G. E., Shooter E. M. Nerve growth factor receptors on PC12 cells: ligand-induced conversion from low- to high-affinity states. Proc Natl Acad Sci U S A. 1980 Aug;77(8):4751–4755. doi: 10.1073/pnas.77.8.4751. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Levi-Montalcini R., Angeletti P. U. Nerve growth factor. Physiol Rev. 1968 Jul;48(3):534–569. doi: 10.1152/physrev.1968.48.3.534. [DOI] [PubMed] [Google Scholar]
  25. Lubin M., Cahn F., Coutermarsh B. A. Amiloride, protein synthesis, and activation of quiescent cells. J Cell Physiol. 1982 Nov;113(2):247–251. doi: 10.1002/jcp.1041130210. [DOI] [PubMed] [Google Scholar]
  26. Moolenaar W. H., Boonstra J., van der Saag P. T., de Laat S. W. Sodium/proton exchange in mouse neuroblastoma cells. J Biol Chem. 1981 Dec 25;256(24):12883–12887. [PubMed] [Google Scholar]
  27. Moolenaar W. H., Yarden Y., de Laat S. W., Schlessinger J. Epidermal growth factor induces electrically silent Na+ influx in human fibroblasts. J Biol Chem. 1982 Jul 25;257(14):8502–8506. [PubMed] [Google Scholar]
  28. Mummery C. L., Boonstra J., Van Der Saag P. T., de Laat S. W. Modulation of functional and optimal (Na+-K+)ATPase activity during the cell cycle of neuroblastoma cells. J Cell Physiol. 1981 Apr;107(1):1–9. doi: 10.1002/jcp.1041070102. [DOI] [PubMed] [Google Scholar]
  29. Mummery C. L., Boonstra J., van der Saag P. T., de Laat S. W. Modulations of Na+ transport during the cell cycle of neuroblastoma cells. J Cell Physiol. 1982 Jul;112(1):27–34. doi: 10.1002/jcp.1041120106. [DOI] [PubMed] [Google Scholar]
  30. O'Lague P. H., Huttner S. L. Physiological and morphological studies of rat pheochromocytoma cells (PC12) chemically fused and grown in culture. Proc Natl Acad Sci U S A. 1980 Mar;77(3):1701–1705. doi: 10.1073/pnas.77.3.1701. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Revoltella R. P., Butler R. H. Nerve growth factor may stimulate either division or differentiation of cloned C1300 neuroblastoma cells in serum-free cultures. J Cell Physiol. 1980 Jul;104(1):27–33. doi: 10.1002/jcp.1041040105. [DOI] [PubMed] [Google Scholar]
  32. Rozengurt E., Heppel L. A. Serum rapidly stimulates ouabain-sensitive 86-RB+ influx in quiescent 3T3 cells. Proc Natl Acad Sci U S A. 1975 Nov;72(11):4492–4495. doi: 10.1073/pnas.72.11.4492. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Rozengurt E., Mendoza S. Monovalent ion fluxes and the control of cell proliferation in cultured fibroblasts. Ann N Y Acad Sci. 1980;339:175–190. doi: 10.1111/j.1749-6632.1980.tb15977.x. [DOI] [PubMed] [Google Scholar]
  34. Schechter A. L., Bothwell M. A. Nerve growth factor receptors on PC12 cells: evidence for two receptor classes with differing cytoskeletal association. Cell. 1981 Jun;24(3):867–874. doi: 10.1016/0092-8674(81)90112-4. [DOI] [PubMed] [Google Scholar]
  35. Schubert D., Whitlock C. Alteration of cellular adhesion by nerve growth factor. Proc Natl Acad Sci U S A. 1977 Sep;74(9):4055–4058. doi: 10.1073/pnas.74.9.4055. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Skaper S. D., Varon S. Mutually independent cyclic AMP and sodium responses to nerve growth factor in embryonic chick dorsal root ganglia. J Neurochem. 1981 Jul;37(1):222–228. doi: 10.1111/j.1471-4159.1981.tb05312.x. [DOI] [PubMed] [Google Scholar]
  37. Skaper S. D., Varon S. Nerve growth factor influences potassium movements in chick embryo dorsal root ganglionic cells. Exp Cell Res. 1981 Feb;131(2):353–361. doi: 10.1016/0014-4827(81)90238-x. [DOI] [PubMed] [Google Scholar]
  38. Skaper S. D., Varon S. Nerve growth factor influences sodium ion extrusion from chick embryonic dorsal root ganglionic neurons. Biochem Biophys Res Commun. 1979 May 28;88(2):563–568. doi: 10.1016/0006-291x(79)92085-0. [DOI] [PubMed] [Google Scholar]
  39. Smith J. B., Rozengurt E. Serum stimulates the Na+,K+ pump in quiescent fibroblasts by increasing Na+ entry. Proc Natl Acad Sci U S A. 1978 Nov;75(11):5560–5564. doi: 10.1073/pnas.75.11.5560. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Taub M., Saier M. H., Jr Amiloride-resistant Madin-Darby canine kidney (MDCK) cells exhibit decreased cation transport. J Cell Physiol. 1981 Feb;106(2):191–199. doi: 10.1002/jcp.1041060204. [DOI] [PubMed] [Google Scholar]
  41. Tischler A. S., Greene L. A. Nerve growth factor-induced process formation by cultured rat pheochromocytoma cells. Nature. 1975 Nov 27;258(5533):341–342. doi: 10.1038/258341a0. [DOI] [PubMed] [Google Scholar]
  42. Varon S. Nerve growth factor and its mode of action. Exp Neurol. 1975 Sep;48(3 Pt 2):75–92. doi: 10.1016/0014-4886(75)90172-7. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES