Cell Cycle Arrest of Proliferating Neuronal Cells by Serum Deprivation Can Result in Either Apoptosis or Differentiation

Abstract: Apoptotic cell death plays a critical role in the development of the nervous system. The death of mature nondividing neurons that fail to receive appropriate input from the target field has been extensively studied. However, the mechanisms mediating the extensive cell death occurring in areas of the developing brain where proliferating neuroblasts differentiate into mature nondividing neurons have not been analyzed. We show here that the cell cycle arrest of a proliferating cell of neuronal origin by removal of serum results in either apoptotic cell death or differentiation to a mature nondividing neuronal cell. The proportion of cells undergoing death or differentiation is influenced in opposite directions by treatment of the cells with cyclic AMP and retinoic acid. This suggests that following the withdrawal of signals stimulating neuroblast cell division, neuronal cells either can cease to suppress a constitutive suicide pathway and hence die by apoptosis or, alternatively, can differentiate into a mature neuronal cell. Regulation of the balance between apoptosis and neuronal differentiation could therefore play a critical role in controlling the numbers of mature neurons that form.

[1]  M. Raff,et al.  Social controls on cell survival and cell death , 1992, Nature.

[2]  N. Thomas,et al.  The retinoblastoma protein is partially phosphorylated during early G1 in cycling cells but not in G1 cells arrested with alpha-interferon. , 1992, Oncogene.

[3]  D. Latchman,et al.  Intracellular redistribution of neuropeptides and secretory proteins during differentiation of neuronal cell lines , 1992, Neuroscience.

[4]  I Nicoletti,et al.  A rapid and simple method for measuring thymocyte apoptosis by propidium iodide staining and flow cytometry. , 1991, Journal of immunological methods.

[5]  J. D. Young,et al.  Cell Death Mechanisms and the Immune System , 1991, Immunological reviews.

[6]  L. Ghibelli,et al.  The expression of "tissue" transglutaminase in two human cancer cell lines is related with the programmed cell death (apoptosis). , 1991, European journal of cell biology.

[7]  Elena Cattaneo,et al.  Proliferation and differentiation of neuronal stem cells regulated by nerve growth factor , 1990, Nature.

[8]  S. Bevan,et al.  Novel cell lines display properties of nociceptive sensory neurons , 1990, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[9]  M. Collins,et al.  Regulation of apoptosis in interleukin‐3‐dependent hemopoietic cells by interleukin‐3 and calcium ionophores. , 1990, The EMBO journal.

[10]  D. Martin,et al.  Cytosine arabinoside kills postmitotic neurons in a fashion resembling trophic factor deprivation: evidence that a deoxycytidine-dependent process may be required for nerve growth factor signal transduction , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[11]  R. Oppenheim The neurotrophic theory and naturally occurring motoneuron death , 1989, Trends in Neurosciences.

[12]  K. Sulik,et al.  Retinoic-acid-induced limb-reduction defects: perturbation of zones of programmed cell death as a pathogenetic mechanism. , 1989, Teratology.

[13]  Yves-Alain Barde,et al.  Trophic factors and neuronal survival , 1989, Neuron.

[14]  David L. Vaux,et al.  Bcl-2 gene promotes haemopoietic cell survival and cooperates with c-myc to immortalize pre-B cells , 1988, Nature.

[15]  P. Distefano,et al.  Inhibitors of protein synthesis and RNA synthesis prevent neuronal death caused by nerve growth factor deprivation , 1988, The Journal of cell biology.

[16]  L. Greene,et al.  cAMP analogs promote survival and neurite outgrowth in cultures of rat sympathetic and sensory neurons independently of nerve growth factor. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[17]  H. Horvitz,et al.  Genetic control of programmed cell death in the nematode C. elegans , 1986, Cell.

[18]  A. Ruusala,et al.  Retinoic acid-induced differentiation of cultured human neuroblastoma cells: a comparison with phorbolester-induced differentiation. , 1984, Cell differentiation.

[19]  J. Sulston,et al.  The embryonic cell lineage of the nematode Caenorhabditis elegans. , 1983, Developmental biology.

[20]  M. Sporn,et al.  Role of retinoids in differentiation and carcinogenesis. , 1983, Cancer research.

[21]  J Steinkamp,et al.  Cell heterogeneity during the cell cycle , 1982, Journal of cellular physiology.

[22]  S. Simpson,et al.  Rapid appearance of labeled degenerating cells in the dorsal root ganglia after exposure of chick embryos to tritiated thymidine. , 1981, Brain research.

[23]  V. Hamburger,et al.  Neuronal death in the spinal ganglia of the chick embryo and its reduction by nerve growth factor , 1981, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[24]  A. Wyllie Glucocorticoid-induced thymocyte apoptosis is associated with endogenous endonuclease activation , 1980, Nature.

[25]  L. Greene,et al.  Quantitative in vitro studies on the nerve growth factor (NGF) requirement of neurons. I. Sympathetic neurons. , 1977, Developmental biology.

[26]  K. Prasad DIFFERENTIATION OF NEUROBLASTOMA CELLS IN CULTURE , 1975, Biological reviews of the Cambridge Philosophical Society.

[27]  R. Oppenheim Cell death during development of the nervous system. , 1991, Annual review of neuroscience.

[28]  C. Weill,et al.  Prevention of natural motoneurone cell death by dibutyryl cyclic GMP , 1984, Nature.

[29]  A. Wyllie,et al.  Cell death: the significance of apoptosis. , 1980, International review of cytology.

[30]  B. Kaellen DEGENERATION AND REGENERATION IN THE VERTEBRATE CENTRAL NERVOUS SYSTEM DURING EMBRYOGENESIS. , 1965, Progress in brain research.