Apoptotic Cell Death of a Hybrid Motoneuron Cell Line Induced by Immunoglobulins from Patients with Amyotrophic Lateral Sclerosis

Abstract: Apoptotic cell death has recently been implicated in diseases involving nonproliferating, terminally differentiated cells such as neurons. Previous experiments have documented that immunoglobulins from patients with amyotrophic lateral sclerosis (ALS) can kill motoneuron‐neuroblastoma hybrid cells [ventral spinal cord 4.1 (VSC 4.1)] by a calcium‐dependent process. Here, we studied the mechanism of ALS IgG‐induced cell death. In the presence of ALS IgG the VSC 4.1 cells undergo cell shrinkage and membrane blebbing, which are morphological features of apoptotic cell death. The damaged cells can be identified by in situ end labeling of nicked DNA and biochemically show laddering on agarose gel electrophoresis. This ALS IgG‐triggered process is prevented by cycloheximide, aurintricarboxylic acid, and zinc sulfate. These data demonstrate that immunoglobulins from patients with ALS are able to induce apoptosis in motoneuron hybrid cells and provide a potential mechanism for motoneuron degeneration in human ALS.

[1]  K. Hsiao,et al.  Neurotoxicity of the prion protein , 1994, Neurobiology of Aging.

[2]  J. Rothstein,et al.  Chronic inhibition of superoxide dismutase produces apoptotic death of spinal neurons. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[3]  P. Barr,et al.  Apoptosis and Its Role in Human Disease , 1994, Bio/Technology.

[4]  E. Stefani,et al.  Cytotoxicity of immunoglobulins from amyotrophic lateral sclerosis patients on a hybrid motoneuron cell line. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[5]  T. Murphy,et al.  Rapid Communication: Oxidative Stress Induces Apoptosis in Embryonic Cortical Neurons , 1994, Journal of neurochemistry.

[6]  B. Barres,et al.  Programmed cell death and the control of cell survival: lessons from the nervous system. , 1993, Science.

[7]  D. Schoepp,et al.  Aurintricarboxylic Acid Prevents NMDA‐Mediated Excitotoxicity: Evidence for Its Action as an NMDA Receptor Antagonist , 1993, Journal of neurochemistry.

[8]  M. E. Lewis,et al.  Aurintricarboxylic Acid Protects Hippocampal Neurons from NMDA‐and Ischemia‐Induced Toxicity In Vivo , 1993, Journal of neurochemistry.

[9]  J. Dubinsky,et al.  Aurintricarboxylic Acid Protects Hippocampal Neurons from Glutamate Excitotoxicity In Vitro , 1993, Journal of neurochemistry.

[10]  D. Carson,et al.  Apoptosis and disease , 1993, The Lancet.

[11]  A. Pizzey,et al.  Cell Cycle Arrest of Proliferating Neuronal Cells by Serum Deprivation Can Result in Either Apoptosis or Differentiation , 1993, Journal of neurochemistry.

[12]  P. Hall,et al.  In situ end‐labelling detects DNA strand breaks in apoptosis and other physiological and pathological states , 1993, The Journal of pathology.

[13]  G. Forloni,et al.  Neurotoxicity of a prion protein fragment , 1993, Nature.

[14]  E. Stefani,et al.  Serum antibodies to L-type calcium channels in patients with amyotrophic lateral sclerosis. , 1992, The New England journal of medicine.

[15]  S. Ben‐Sasson,et al.  Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation , 1992, The Journal of cell biology.

[16]  M. Mattson,et al.  beta-Amyloid peptides destabilize calcium homeostasis and render human cortical neurons vulnerable to excitotoxicity , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[17]  L. Greene,et al.  Aurintricarboxylic acid rescues PC12 cells and sympathetic neurons from cell death caused by nerve growth factor deprivation: correlation with suppression of endonuclease activity , 1991, The Journal of cell biology.

[18]  T. Yoshimoto,et al.  Glutamate triggers internucleosomal DNA cleavage in neuronal cells. , 1991, Biochemical and biophysical research communications.

[19]  J. Kerr Definition and incidence of apoptosis : A historical perspective , 1991 .