Biochemical and electrophysiological differentiation profile of a human neuroblastoma (IMR-32) cell line

In Vitro Cellular and Developmental Biology - Animal

Volumn 38, Issue 8, 2002, Pages 450-456

  Rao, Raj R ^a   Kisaalita, William S ^a  

^a University of Georgia   (United States)

Author keywords

Cellular engineering; Confocal microscopy; Flow cytometry; Neuron specific enolase; Resting membrane potential

Indexed keywords

NEURON SPECIFIC ENOLASE; PHOSPHOENOLPYRUVATE;

ARTICLE; CANCER CELL CULTURE; CELL DIFFERENTIATION; CONFOCAL MICROSCOPY; CONTROLLED STUDY; CORRELATION ANALYSIS; ELECTROPHYSIOLOGY; ENZYME ACTIVITY; FLOW CYTOMETRY; HUMAN; HUMAN CELL; IN VITRO STUDY; MAGNETIC FIELD; MEMBRANE STEADY POTENTIAL; NEUROBLASTOMA; POTENTIOMETRY;

CELL DIFFERENTIATION; FLOW CYTOMETRY; FLUORESCENCE; HUMANS; NEUROBLASTOMA; PHOSPHOPYRUVATE HYDRATASE; TUMOR CELLS, CULTURED;

MURINAE;

EID: 0036764964     PISSN: 10712690     EISSN: None     Source Type: Journal    
DOI: 10.1290/1071-2690(2002)038<0450:BAEDPO>2.0.CO;2     Document Type: Article

References (32)

1. Anderson, J. P.; Esch, F. S.; Keim, P. S.; Sambamurti, K.; Leiberburg, I.; Robakis, N. K. Exact cleavage site of Alzheimer amyloid precursor in neuronal PC12 cells. Neurosci. Lett. 128:126-128; 1991.
2. Baranowski, T.; Wolna, E. Enolase from human muscle. Methods Enzymol. 42:335-338; 1975.
3. Brashford, C. L.; Alder, G. M.; Gray, M. A.; Micklem, K. J.; Taylor, C. C.; Turek, T.; Pasternak, C. A. Oxonol dyes as monitors of membrane potential of animal cells in monolayer culture and in suspension. J. Cell. Physiol. 123:326-336; 1985.
4. Bräuner, T.; Hülser, T. F.; Strasser, R. J. Comparative measurements of membrane potentials with microelectrodes and voltage-sensitive dyes. Biochim. Biophys. Acta 771:208-216; 1984.
5. Day, I. N. M. Enolases and PGP 9.5 as tissue specific marker. Biochem. Soc. Trans. 20:637-642; 1992.
6. Ehrenberg, B.; Montana, V.; Wei, M. D.; Wuskell, J. P.; Loew, L. M. Membrane potential can be determined in individual cells from the Nernstian distribution of cationic dyes. Biophys. J. 53(5):785-794; 1998.
7. Emaus, R. K.; Grunwald, R.; Lemasters, J. J. Rhodamine 123 as a probe of transmembrane potential in isolated rat-liver mitochondria: spectral and metabolic properties. Biochim. Biophys. Acta 850(3):436-448; 1986.
8. Esch, F. S.; Keim, P. S.; Beattie, E. C.; Blacher, R. W.; Culwell, A. R.; Oltersdorf, T.; McClure, D.; Ward, P. J. Cleavage of amyloid beta peptide during constitutive processing of its precursor. Science 248(4959):1122-1124; 1990.
9. Fletcher, L.; Rider, C. C.; Taylor, C. B.; Adamson, E. D.; Luke, B. M.; Graham, C. F. Enolase isozymes: chromatographic and immunological characteristics of rat brain enolase. Biochim. Biophys. Acta 452:245-252; 1978.
10. Fukuchi, K.-I.; Kamino, K.; Deeb, S. S.; Furlong, C. E.; Sundstrom, J. A.; Martin, A. C.; Martin, G. M. Expression of a carboxy-terminal region of the β-amyloid precursor protein in a heterogeneous culture of neuroblastoma cells: evidence for altered processing and selective neurotoxicicty. Mol. Brain Res. 16:37-46; 1992.
11. Ginsborg, B. L.; Martin, R. J.; Patmore, L. On the sodium and potassium currents of a human neuroblastoma cell line. J. Physiol. (Lond.) 434:121-149; 1991.
12. 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 34(2):144-155; 1987.
13. Hernandez, M.; Kisaalita, W. S.; Farmer, M. A. Assessment of murine neuroblastoma (N1E-115) resting membrane potential by confocal microscopy. J. Fluorescence 6(2):77-82; 1996.
14. Ishikawa, S. Differentiation of human neuroblastoma cells in-vitro - morphological changes induced by dibutyryl cyclic AMP. Acta Path. Jpn. 27:697-711; 1977.
15. Kisaalita, W. S.; Bowen, J. M. Effect of culture age on the susceptibility of differentiating neuroblastoma cells to retinoid cytotoxicity. Biotechnol. Bioeng. 50:580-586; 1996.
16. Kisaalita, W. S.; Bowen, J. M. Development of resting membrane potentials in differentiating murine neuroblastoma cells (N1E-115) evaluated by flow cytometry. Cytotechnology 24:201-212; 1997.
17. Kohen, E.; Hirschberg, J. A. Cell structure and function by microspectrofluorometry. San Diego, CA: Academic Press; 1989.
18. Lahiri, D. K. The stability of β-amyloid precursor protein in nine different cell types. Biochem. Mol. Biol. Int. 29(5):849-858; 1993.
19. Marangos, P. J.; Goodwin, F. K.; Parma, A. M.; Leuter, C.; Trams, E. Neuron-specific protein (NSP) in neuroblastoma cells in relation to differentiation. Brain Res. 145:49-58; 1978.
20. Masters, C. L.; Simms, G.; Weinman, N. A.; Multhap, G.; McDonald, B. L; Beyreuther, K. Amyloid plaque core protein in Alzheimer disease and down syndrome. Proc. Natl. Acad. Sci. USA 82:4245-4249; 1985.
21. Mummery, C. L.; Van den Brink, C. E.; Van der Saag, P. T.; De Laat, S. W. A short-term screening test for teratogens using differentiating neuroblastoma cells in vitro. Teratology 29(2):271-279; 1984.
22. Neill, D.; Hughes, D.; Edwardson, J. A.; Rima, B. K.; Allsop, D. Human IMR-32 neuroblastoma cells as a model cell line in Alzheimer's disease research. J. Neurosci. 39(4):482-493; 1994.
23. Odelstad, L.; Pahlman, S.; Nilsson, K.; Larsson, E.; Lackgren, G.; Johansson, K. E.; Hjerten, S.; Grotte, G. Neuron-specific enolase in relation to differentiation in human neuroblastoma. Brain Res. 224(1):69-82; 1981.
24. Rao, R. R.; Halper, J.; Kisaalita, W. S. Effects of 60 Hz electromagnetic field exposure on APP695 transcription in differentiating human neuroblastoma cells. Bioelectrochemistry 57:9-15; 2002.
25. Schmechel, D. E.; Brightman, M. W.; Marangos, P. J. Neurons switch from non-neuronal enolase to neuron-specific enolase during differentiation. Brain Res. 190:195-214; 1980.
26. Shamblott, M. J.; Axelman, J.; Wang, S., et al. Derivation of pluripotent stem cells from cultured human primordial germ cells [published erratum appears in Proc. Natl. Acad. Sci. USA 96(3):1162; 1999]. Proc. Natl. Acad. Sci. USA 95(23):13726-13731; 1998.
27. Sobel, E.; Davanipour, Z. Electromagnetic field exposure may cause increased production of amyloid beta and eventually lead to Alzheimer's disease. Neurology 47:1594-1600; 1996.
28. Thomson, J. A.; Itskovitz-Eldor, J.; Shapiro, S. S.; Waknitz, M. A.; Swiergiel, J. J.; Marshall, V. S.; Jones, J. M. Embryonic stem cell lines derived from human blastocysts [see comments; published eratum appears in Science 282(5395):1827; 1998]. Science 282(5391):1145-1147; 1998.
29. Tumilocwicz, J. J.; Nichols, W. W.; Cholon, J. J.; Greene, A. E. Definition of a continuous human cell line derived from neuroblastoma. Cancer Res. 30:2110-2118; 1970.
30. Walsh, D. M.; Williams, C. H.; Kennedy, H. E.; Murphy, G.; Allsop, D. Gelatinase A not alpha-secretase? Nature 367:27-28; 1994.
31. Wang, R.; Meschia, J. F.; Cotter, R. J.; Sisodia, S. S. Secretion of the beta/ A4 amyloid precursor protein. Identification of a cleavage site in cultured mammalian cells. J. Biol. Chem. 266(25):16960-16964; 1991.
32. 2+-sensitive potassium channels described by oxonol dye fluorescence measurements. J. Cell. Physiol. 125:72-81; 1985.