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Altered ceramide acyl chain length and ceramide synthase gene expression in Parkinson’s disease

Journal Article


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Abstract


  • Genetic studies have provided increasing evidence that ceramide homeostasis plays a role in neurodegenerative diseases including Parkinson's disease (PD). It is known that the relative amounts of different ceramide molecular species, as defined by their fatty acyl chain length, regulate ceramide function in lipid membranes and in signaling pathways. In the present study we used a comprehensive sphingolipidomic case-control approach to determine the effects of PD on ceramide composition in postmortem brain tissue from the anterior cingulate cortex (a region with significant PD pathology) and the occipital cortex (spared in PD), also assessing mRNA expression of the major ceramide synthase genes that regulate ceramide acyl chain composition in the same tissue using quantitative PCR. In PD anterior cingulate cortex but not occipital cortex, total ceramide and sphingomyelin levels were reduced from control levels by 53% (P < 0.001) and 42% (P < 0.001), respectively. Of the 13 ceramide and 15 sphingomyelin molecular lipid species identified and quantified, there was a significant shift in the ceramide acyl chain composition toward shorter acyl chain length in the PD anterior cingulate cortex. This PD-associated change in ceramide acyl chain composition was accompanied by an upregulation of ceramide synthase-1 gene expression, which we consider may represent a response to reduced ceramide levels. These data suggest a significant shift in ceramide function in lipid membranes and signaling pathways occurs in regions with PD pathology. Identifying the regulatory mechanisms precipitating this change may provide novel targets for future therapeutics.

Publication Date


  • 2014

Citation


  • Abbott, S. K., Li, H., Sanz Munoz, S., Knoch, B., Batterham, M., Murphy, K. E., Halliday, G. M. & Garner, B. (2014). Altered ceramide acyl chain length and ceramide synthase gene expression in Parkinson’s disease. Movement Disorders, 29 (4), 518-526.

Scopus Eid


  • 2-s2.0-84898057274

Ro Full-text Url


  • http://ro.uow.edu.au/cgi/viewcontent.cgi?article=1450&context=ihmri

Ro Metadata Url


  • http://ro.uow.edu.au/ihmri/433

Has Global Citation Frequency


Number Of Pages


  • 8

Start Page


  • 518

End Page


  • 526

Volume


  • 29

Issue


  • 4

Place Of Publication


  • United States

Abstract


  • Genetic studies have provided increasing evidence that ceramide homeostasis plays a role in neurodegenerative diseases including Parkinson's disease (PD). It is known that the relative amounts of different ceramide molecular species, as defined by their fatty acyl chain length, regulate ceramide function in lipid membranes and in signaling pathways. In the present study we used a comprehensive sphingolipidomic case-control approach to determine the effects of PD on ceramide composition in postmortem brain tissue from the anterior cingulate cortex (a region with significant PD pathology) and the occipital cortex (spared in PD), also assessing mRNA expression of the major ceramide synthase genes that regulate ceramide acyl chain composition in the same tissue using quantitative PCR. In PD anterior cingulate cortex but not occipital cortex, total ceramide and sphingomyelin levels were reduced from control levels by 53% (P < 0.001) and 42% (P < 0.001), respectively. Of the 13 ceramide and 15 sphingomyelin molecular lipid species identified and quantified, there was a significant shift in the ceramide acyl chain composition toward shorter acyl chain length in the PD anterior cingulate cortex. This PD-associated change in ceramide acyl chain composition was accompanied by an upregulation of ceramide synthase-1 gene expression, which we consider may represent a response to reduced ceramide levels. These data suggest a significant shift in ceramide function in lipid membranes and signaling pathways occurs in regions with PD pathology. Identifying the regulatory mechanisms precipitating this change may provide novel targets for future therapeutics.

Publication Date


  • 2014

Citation


  • Abbott, S. K., Li, H., Sanz Munoz, S., Knoch, B., Batterham, M., Murphy, K. E., Halliday, G. M. & Garner, B. (2014). Altered ceramide acyl chain length and ceramide synthase gene expression in Parkinson’s disease. Movement Disorders, 29 (4), 518-526.

Scopus Eid


  • 2-s2.0-84898057274

Ro Full-text Url


  • http://ro.uow.edu.au/cgi/viewcontent.cgi?article=1450&context=ihmri

Ro Metadata Url


  • http://ro.uow.edu.au/ihmri/433

Has Global Citation Frequency


Number Of Pages


  • 8

Start Page


  • 518

End Page


  • 526

Volume


  • 29

Issue


  • 4

Place Of Publication


  • United States