A natural human IgM that binds to gangliosides is therapeutic in murine models of amyotrophic lateral sclerosis

Xiaohua Xu, Aleksandar Denic, Luke R. Jordan, Nathan J. Wittenberg, Arthur E. Warrington, Bharath Wootla, Louisa M. Papke, Laurie J. Zoecklein, Daehan Yoo, Jonah Shaver, Sang Hyun Oh, Larry R. Pease, Moses Rodriguez

Research output: Contribution to journalArticle

21 Scopus citations

Abstract

Amyotrophic lateral sclerosis (ALS) is a devastating, fatal neurological disease that primarily affects spinal cord anterior horn cells and their axons for which there is no treatment. Here we report the use of a recombinant natural human IgM that binds to the surface of neurons and supports neurite extension, rHIgM12, as a therapeutic strategy in murine models of human ALS. A single 200 μg intraperitoneal dose of rHIgM12 increases survival in two independent genetic-based mutant SOD1 mouse strains (SOD1G86R andSOD1G93A) by 8 and 10 days, delays the onset of neurological deficits by 16 days, delays the onset of weight loss by 5 days, and preserves spinal cord axons and anterior horn neurons. Immuno-overlay of thin layer chromatography and surface plasmon resonance show that rHIgM12 binds with high affinity to the complex gangliosides GD1a and GT1b. Addition of rHIgM12 to neurons in culture increases a-tubulin tyrosination levels, suggesting an alteration of microtubule dynamics. We previously reported that a single peripheral dose of rHIgM12 preserved neurological function in a murine model of demyelination with axon loss. Because rHIgM12 improves three different models of neurological disease, we propose that the IgM might act late in the cascade of neuronal stress and/or death by a broad mechanism.

Original languageEnglish (US)
Pages (from-to)831-842
Number of pages12
JournalDMM Disease Models and Mechanisms
Volume8
Issue number8
DOIs
StatePublished - Aug 1 2015

Keywords

  • ALS
  • Amyotrophic lateral sclerosis
  • Axon growth
  • GD1a
  • GT1b
  • Gangliosides
  • Neurite extension
  • Neuroprotection
  • SOD1
  • SPR
  • Supported lipid bilayers
  • Surface plasmon resonance

ASJC Scopus subject areas

  • Neuroscience (miscellaneous)
  • Medicine (miscellaneous)
  • Immunology and Microbiology (miscellaneous)
  • Biochemistry, Genetics and Molecular Biology(all)

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