Abstract
IMR-32 human neuroblastoma cells are unable to release [3H]dopamine in response to secretagogues. However, they express a normal complement of membrane receptors and ion channels which are efficiently coupled to second messenger production. In the present study we took advantage of the ability of this cell line to differentiate in vitro in the presence of either dibutyrryl-cAMP or 5-bromodeoxyuridine, to analyze any developmentally regulated changes in its secretory properties. Uptake, storage, and release of [3H]dopamine were studied biochemically and by autoradiography. The calcium ionophore ionomycin, phorbol 12-myristate 13-acetate and the presynaptic acting neurotoxin alpha-latrotoxin were used in both control and differentiated cells as secretagogue agents. The presence of secretory organelles was investigated by electron microscopy; the expression of secretory organelle markers, such as chromogranin/secretogranin proteins (secretory proteins) and synaptophysin (membrane protein), was detected by Western blotting and immunofluorescence. The results obtained indicate that IMR-32 cells acquire regulated secretory properties after in vitro drug-induced differentiation: (a) they assemble "de novo" secretory organelles, as revealed by electron microscopy and detection of secretory organelle markers, and (b) they are able to store [3H]dopamine and to release the neurotransmitter in response to secretagogue stimuli. Furthermore, secretagogue sensitivity was found to be different, depending on the differentiating agent. In fact, dibutyrryl-cAMP treated cells release [3H]dopamine in response to alpha-latrotoxin, but not in response to ionomycin, whereas 5-bromodeoxyuridine treated cells release the neurotransmitter in response to both secretagogues. All together these results suggest that IMR-32 cells represent an adequate model for studying the development of the secretory apparatus in cultured human neurons.
Full Text
The Full Text of this article is available as a PDF (3.2 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Augustine G. J., Charlton M. P., Smith S. J. Calcium action in synaptic transmitter release. Annu Rev Neurosci. 1987;10:633–693. doi: 10.1146/annurev.ne.10.030187.003221. [DOI] [PubMed] [Google Scholar]
- Barrowman M. M., Cockcroft S., Gomperts B. D. Two roles for guanine nucleotides in the stimulus-secretion sequence of neutrophils. Nature. 1986 Feb 6;319(6053):504–507. doi: 10.1038/319504a0. [DOI] [PubMed] [Google Scholar]
- Bell C. Dopamine release from sympathetic nerve terminals. Prog Neurobiol. 1988;30(2-3):193–208. doi: 10.1016/0301-0082(88)90006-8. [DOI] [PubMed] [Google Scholar]
- Bethea C. L., Rønnekleiv O. K., Kozak S. L. Extracellular matrix changes PC12 cell shape and processing of newly synthesized dopamine. Mol Cell Endocrinol. 1987 Nov;54(1):63–79. doi: 10.1016/0303-7207(87)90140-7. [DOI] [PubMed] [Google Scholar]
- Bittner M. A., Holz R. W., Neubig R. R. Guanine nucleotide effects on catecholamine secretion from digitonin-permeabilized adrenal chromaffin cells. J Biol Chem. 1986 Aug 5;261(22):10182–10188. [PubMed] [Google Scholar]
- Burgoyne R. D. G proteins: control of exocytosis. Nature. 1987 Jul 9;328(6126):112–113. doi: 10.1038/328112a0. [DOI] [PubMed] [Google Scholar]
- Burnette W. N. "Western blotting": electrophoretic transfer of proteins from sodium dodecyl sulfate--polyacrylamide gels to unmodified nitrocellulose and radiographic detection with antibody and radioiodinated protein A. Anal Biochem. 1981 Apr;112(2):195–203. doi: 10.1016/0003-2697(81)90281-5. [DOI] [PubMed] [Google Scholar]
- Caughey B., Kirshner N. Effects of reserpine and tetrabenazine on catecholamine and ATP storage in cultured bovine adrenal medullary chromaffin cells. J Neurochem. 1987 Aug;49(2):563–573. doi: 10.1111/j.1471-4159.1987.tb02901.x. [DOI] [PubMed] [Google Scholar]
- Clementi F., Cabrini D., Gotti C., Sher E. Pharmacological characterization of cholinergic receptors in a human neuroblastoma cell line. J Neurochem. 1986 Jul;47(1):291–297. doi: 10.1111/j.1471-4159.1986.tb02861.x. [DOI] [PubMed] [Google Scholar]
- Eiden L. E., Huttner W. B., Mallet J., O'Connor D. T., Winkler H., Zanini A. A nomenclature proposal for the chromogranin/secretogranin proteins. Neuroscience. 1987 Jun;21(3):1019–1021. doi: 10.1016/0306-4522(87)90056-x. [DOI] [PubMed] [Google Scholar]
- Frontali N., Ceccarelli B., Gorio A., Mauro A., Siekevitz P., Tzeng M. C., Hurlbut W. P. Purification from black widow spider venom of a protein factor causing the depletion of synaptic vesicles at neuromuscular junctions. J Cell Biol. 1976 Mar;68(3):462–479. doi: 10.1083/jcb.68.3.462. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Geiger B., Singer S. J. The participation of alpha-actinin in the capping of cell membrane components. Cell. 1979 Jan;16(1):213–222. doi: 10.1016/0092-8674(79)90202-2. [DOI] [PubMed] [Google Scholar]
- Gotti C., Sher E., Cabrini D., Bondiolotti G., Wanke E., Mancinelli E., Clementi F. Cholinergic receptors, ion channels, neurotransmitter synthesis, and neurite outgrowth are independently regulated during the in vitro differentiation of a human neuroblastoma cell line. Differentiation. 1987;34(2):144–155. doi: 10.1111/j.1432-0436.1987.tb00061.x. [DOI] [PubMed] [Google Scholar]
- Gotti C., Wanke E., Sher E., Fornasari D., Cabrini D., Clementi F. Acetylcholine operated ion channel and alpha-bungarotoxin binding site in a human neuroblastoma cell line reside on different molecules. Biochem Biophys Res Commun. 1986 Jun 30;137(3):1141–1147. doi: 10.1016/0006-291x(86)90344-x. [DOI] [PubMed] [Google Scholar]
- Gupta M., Notter M. F., Felten S., Gash D. M. Differentiation characteristics of human neuroblastoma cells in the presence of growth modulators and antimitotic drugs. Brain Res. 1985 Mar;351(1):21–29. doi: 10.1016/0165-3806(85)90227-5. [DOI] [PubMed] [Google Scholar]
- HOFSTEE B. H. Non-inverted versus inverted plots in enzyme kinetics. Nature. 1959 Oct 24;184:1296–1298. doi: 10.1038/1841296b0. [DOI] [PubMed] [Google Scholar]
- Knaus P., Betz H., Rehm H. Expression of synaptophysin during postnatal development of the mouse brain. J Neurochem. 1986 Oct;47(4):1302–1304. doi: 10.1111/j.1471-4159.1986.tb00754.x. [DOI] [PubMed] [Google Scholar]
- Kretsinger R. H., Creutz C. E. Cell biology. Consensus in exocytosis. Nature. 1986 Apr 17;320(6063):573–573. doi: 10.1038/320573a0. [DOI] [PubMed] [Google Scholar]
- Lee R. W., Huttner W. B. Tyrosine-O-sulfated proteins of PC12 pheochromocytoma cells and their sulfation by a tyrosylprotein sulfotransferase. J Biol Chem. 1983 Sep 25;258(18):11326–11334. [PubMed] [Google Scholar]
- Lowe A. W., Madeddu L., Kelly R. B. Endocrine secretory granules and neuronal synaptic vesicles have three integral membrane proteins in common. J Cell Biol. 1988 Jan;106(1):51–59. doi: 10.1083/jcb.106.1.51. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Meldolesi J., Huttner W. B., Tsien R. Y., Pozzan T. Free cytoplasmic Ca2+ and neurotransmitter release: studies on PC12 cells and synaptosomes exposed to alpha-latrotoxin. Proc Natl Acad Sci U S A. 1984 Jan;81(2):620–624. doi: 10.1073/pnas.81.2.620. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Navone F., Jahn R., Di Gioia G., Stukenbrok H., Greengard P., De Camilli P. Protein p38: an integral membrane protein specific for small vesicles of neurons and neuroendocrine cells. J Cell Biol. 1986 Dec;103(6 Pt 1):2511–2527. doi: 10.1083/jcb.103.6.2511. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Neher E. The influence of intracellular calcium concentration on degranulation of dialysed mast cells from rat peritoneum. J Physiol. 1988 Jan;395:193–214. doi: 10.1113/jphysiol.1988.sp016914. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Neuman B., Wiedermann C. J., Fischer-Colbrie R., Schober M., Sperk G., Winkler H. Biochemical and functional properties of large and small dense-core vesicles in sympathetic nerves of rat and ox vas deferens. Neuroscience. 1984 Nov;13(3):921–931. doi: 10.1016/0306-4522(84)90106-4. [DOI] [PubMed] [Google Scholar]
- Obendorf D., Schwarzenbrunner U., Fischer-Colbrie R., Laslop A., Winkler H. In adrenal medulla synaptophysin (protein p38) is present in chromaffin granules and in a special vesicle population. J Neurochem. 1988 Nov;51(5):1573–1580. doi: 10.1111/j.1471-4159.1988.tb01127.x. [DOI] [PubMed] [Google Scholar]
- Pozzan T., Gatti G., Dozio N., Vicentini L. M., Meldolesi J. Ca2+-dependent and -independent release of neurotransmitters from PC12 cells: a role for protein kinase C activation? J Cell Biol. 1984 Aug;99(2):628–638. doi: 10.1083/jcb.99.2.628. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Prasad K. N., Mandal B., Kumar S. Human neuroblastoma cell culture: effect of 5-bromodeoxyuridine on morphological differentiation and levels of neural enzymes. Proc Soc Exp Biol Med. 1973 Oct 1;144(1):38–42. doi: 10.3181/00379727-144-37522. [DOI] [PubMed] [Google Scholar]
- Reynolds C. P., Perez-Polo J. R. Induction of neurite outgrowth in the IMR-32 human neuroblastoma cell line by nerve growth factor. J Neurosci Res. 1981;6(3):319–325. doi: 10.1002/jnr.490060307. [DOI] [PubMed] [Google Scholar]
- Richards M. L., Sadee W. Human neuroblastoma cell lines as models of catechol uptake. Brain Res. 1986 Oct 1;384(1):132–137. doi: 10.1016/0006-8993(86)91228-x. [DOI] [PubMed] [Google Scholar]
- Rosa P., Hille A., Lee R. W., Zanini A., De Camilli P., Huttner W. B. Secretogranins I and II: two tyrosine-sulfated secretory proteins common to a variety of cells secreting peptides by the regulated pathway. J Cell Biol. 1985 Nov;101(5 Pt 1):1999–2011. doi: 10.1083/jcb.101.5.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rupniak H. T., Rein G., Powell J. F., Ryder T. A., Carson S., Povey S., Hill B. T. Characteristics of a new human neuroblastoma cell line which differentiates in response to cyclic adenosine 3':5'-monophosphate. Cancer Res. 1984 Jun;44(6):2600–2607. [PubMed] [Google Scholar]
- Scammell J. G., Burrage T. G., Dannies P. S. Hormonal induction of secretory granules in a pituitary tumor cell line. Endocrinology. 1986 Oct;119(4):1543–1548. doi: 10.1210/endo-119-4-1543. [DOI] [PubMed] [Google Scholar]
- Schober M., Fischer-Colbrie R., Schmid K. W., Bussolati G., O'Connor D. T., Winkler H. Comparison of chromogranins A, B, and secretogranin II in human adrenal medulla and pheochromocytoma. Lab Invest. 1987 Oct;57(4):385–391. [PubMed] [Google Scholar]
- Sher E., Gotti C., Pandiella A., Madeddu L., Clementi F. Intracellular calcium homeostasis in a human neuroblastoma cell line: modulation by depolarization, cholinergic receptors, and alpha-latrotoxin. J Neurochem. 1988 Jun;50(6):1708–1713. doi: 10.1111/j.1471-4159.1988.tb02467.x. [DOI] [PubMed] [Google Scholar]
- Sher E., Pandiella A., Clementi F. Omega-conotoxin binding and effects on calcium channel function in human neuroblastoma and rat pheochromocytoma cell lines. FEBS Lett. 1988 Aug 1;235(1-2):178–182. doi: 10.1016/0014-5793(88)81258-4. [DOI] [PubMed] [Google Scholar]
- Sidell N. Retinoic acid-induced growth inhibition and morphologic differentiation of human neuroblastoma cells in vitro. J Natl Cancer Inst. 1982 Apr;68(4):589–596. [PubMed] [Google Scholar]
- Somogyi P., Hodgson A. J., DePotter R. W., Fischer-Colbrie R., Schober M., Winkler H., Chubb I. W. Chromogranin immunoreactivity in the central nervous system. Immunochemical characterisation, distribution and relationship to catecholamine and enkephalin pathways. Brain Res. 1984 Dec;320(2-3):193–230. doi: 10.1016/0165-0173(84)90007-9. [DOI] [PubMed] [Google Scholar]
- Spinelli W., Sonnenfeld K. H., Ishii D. N. Effects of phorbol ester tumor promoters and nerve growth factor on neurite outgrowth in cultured human neuroblastoma cells. Cancer Res. 1982 Dec;42(12):5067–5073. [PubMed] [Google Scholar]
- Thompson J. M., London E. D., Johnson J. E., Jr Ultrastructural, functional and biochemical characteristics of mouse and human neuroblastoma cell lines. Neuroscience. 1982 Jul;7(7):1807–1815. doi: 10.1016/0306-4522(82)90038-0. [DOI] [PubMed] [Google Scholar]
- Tsien R. Y., Pozzan T., Rink T. J. Calcium homeostasis in intact lymphocytes: cytoplasmic free calcium monitored with a new, intracellularly trapped fluorescent indicator. J Cell Biol. 1982 Aug;94(2):325–334. doi: 10.1083/jcb.94.2.325. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tumilowicz J. J., Nichols W. W., Cholon J. J., Greene A. E. Definition of a continuous human cell line derived from neuroblastoma. Cancer Res. 1970 Aug;30(8):2110–2118. [PubMed] [Google Scholar]
- Vallar L., Biden T. J., Wollheim C. B. Guanine nucleotides induce Ca2+-independent insulin secretion from permeabilized RINm5F cells. J Biol Chem. 1987 Apr 15;262(11):5049–5056. [PubMed] [Google Scholar]
- Winkler H., Apps D. K., Fischer-Colbrie R. The molecular function of adrenal chromaffin granules: established facts and unresolved topics. Neuroscience. 1986 Jun;18(2):261–290. doi: 10.1016/0306-4522(86)90154-5. [DOI] [PubMed] [Google Scholar]
- Zanini A., Rosa P. Characterization of adenohypophysial polypeptides by two-dimensional gel electrophoresis. I. L-[3H]leucine-labeled polypeptides. Mol Cell Endocrinol. 1981 Nov;24(2):165–179. doi: 10.1016/0303-7207(81)90057-5. [DOI] [PubMed] [Google Scholar]