Abstract
Ceramide synthase 2 (CerS2) catalyzes the synthesis of dihydroceramides from dihydrosphingosine and very long fatty acyl (C22–C24)-CoAs. CerS2-deficient (gene trap) mice were reported to exhibit myelin and behavioral abnormalities, associated with the expression of CerS2 in oligodendrocytes and neurons based on expression of lacZ reporter cDNA instead of the cers2 gene in these mice. In order to clarify the cell-type-specific expression of CerS2 protein, we have raised antibodies that specifically recognize the glycosylated and non-glycosylated CerS2 protein in wild-type but not in CerS2-deficient mouse tissues. In early postnatal, juvenile and adult mouse brain, the new antibodies detect CerS2 protein only in oligodendrocytes but not in neurons, suggesting that the gene trap vector in CerS2-deficient mice led to ectopic expression of the lacZ reporter gene in neurons. In liver, the CerS2 protein is expressed in hepatocytes but not in Ito cells or Kupffer cells. We conclude that the behavioral abnormalities observed in CerS2-deficient mice originate primarily in oligodendrocytes and not in neurons. The identification of specific cell types in which CerS2 protein is expressed is prerequisite to further mechanistic characterization of phenotypic abnormalities exhibited by CerS2-deficient mice. The amount of CerS2 protein detected in different tissues by immunoblot analyses does not strictly correspond to the activity of the CerS2 enzyme. Disproportional results are likely due to post-translational regulation of the CerS2 protein.
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Acknowledgments
We thank D. May for providing Cx47EGFP mice, Dr. S. Sonntag for his support during this project and C. Siegmund for excellent technical assistance. Furthermore we thank Prof. M. Egmond (Utrecht) for providing the immunogenic CerS2 peptide. This study was supported by a grant of the German Research Foundation (through SFB 645, B2) to K. W.
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Kremser, C., Klemm, AL., van Uelft, M. et al. Cell-type-specific expression pattern of ceramide synthase 2 protein in mouse tissues. Histochem Cell Biol 140, 533–547 (2013). https://doi.org/10.1007/s00418-013-1091-z
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DOI: https://doi.org/10.1007/s00418-013-1091-z