Motor neuron degeneration correlates with respiratory dysfunction in SCA1

James P. Orengo, Meike E. van der Heijden, Shuang Hao, Jianrong Tang, Harry T. Orr, Huda Y. Zoghbi

Research output: Contribution to journalArticlepeer-review

14 Scopus citations


Spinocerebellar ataxia type 1 (SCA1) is characterized by adult-onset cerebellar degeneration with attendant loss of motor coordination. Bulbar function is eventually impaired and patients typically die from an inability to clear the airway. We investigated whether motor neuron degeneration is at the root of bulbar dysfunction by studying SCA1 knock-in (Atxn1154Q/+) mice. Spinal cord and brainstem motor neurons were assessed in Atxn1154Q/+ mice at 1, 3 and 6 months of age. Specifically, we assessed breathing physiology, diaphragm histology and electromyography, and motor neuron histology and immunohistochemistry. Atxn1154Q/+ mice show progressive neuromuscular respiratory abnormalities, neurogenic changes in the diaphragm, and motor neuron degeneration in the spinal cord and brainstem. Motor neuron degeneration is accompanied by reactive astrocytosis and accumulation of Atxn1 aggregates in the motor neuron nuclei. This observation correlates with previous findings in SCA1 patient tissue. Atxn1154Q/+ mice develop bulbar dysfunction because of motor neuron degeneration. These findings confirm the Atxn1154Q/+ line as a SCA1 model with face and construct validity for this understudied disease feature. Furthermore, this model is suitable for studying the pathogenic mechanism driving motor neuron degeneration in SCA1 and possibly other degenerative motor neuron diseases. From a clinical standpoint, the data indicate that pulmonary function testing and employment of non-invasive ventilator support could be beneficial in SCA1 patients. The physiological tests used in this study might serve as valuable biomarkers for future therapeutic interventions and clinical trials. This article has an associated First Person interview with the first author of the paper.

Original languageEnglish (US)
Article number032623
JournalDMM Disease Models and Mechanisms
Issue number2
StatePublished - Feb 2018

Bibliographical note

Funding Information:
Support for this work comes from an R25 fellowship (NS070680) through the National Institutes of Health/National Institute of Neurological Disorders and Stroke (NIH/NINDS), Mrs Clifford Elder White Graham Endowed Research Fund (Baylor College of Medicine) and the National Ataxia Foundation to J.P.O. Additional support is provided by the American Heart Association (17PRE33660616) to M.E.v.d.H.; the NIH/NINDS (R37 NS027699), the BCM Intellectual and Developmental Disabilities Research Center (IDDRC; NIH/NICHHD U54HD083092) and the Howard Hughes Medical Institute (HHMI) to H.Y.Z.

Publisher Copyright:
© 2018. Published by The Company of Biologists Ltd


  • Bulbar dysfunction
  • Motor neuron degeneration
  • SCA1
  • Spinocerebellar ataxia type 1


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