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Mitochondrial Activity and Morphology are Affected by Sphinganine in Neurospora Crassa.

Published online by Cambridge University Press:  02 July 2020

J. A. Gerlach
Affiliation:
Department of Biology, Utica College of Syracuse University, Utica, NY13502
K. M. Bart
Affiliation:
Department of Biology, Hamilton College, Clinton, NY13323
L. R. Aaronson
Affiliation:
Department of Biology, Utica College of Syracuse University, Utica, NY13502
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Extract

It has been proposed that sphinganine may function as a natural antifungal barrier in mammals. This sphingoid base is found highly concentrated in epidermis, where it has been documented to inhibit the colonization of pathogenic fungi such as Epidermophyton and Candida. Since Neurospora crassa is sensitive to the effects of sphinganine within the same concentration range as infectious fungi, it is being employed as the model to study the mechanism of sphinganine toxicity in fungal pathogens. With the dramatic increase in fungal mycoses seen in immunocompromised individuals to date, this natural constituent of mammalian epidermis may be employed as a potent, novel antifungal drug.

During this project, radioactive labelling with [3H]sphinganine was employed to observe metabolism of exogenous sphinganine into complex sphingolipids. Transmission electron microscopy analysis was utilized to observe changes in cellular ultrastructure, while fluorescence microscopic techniques were used to assay certain cell functions.

Within 1 hr, exogenous sources of sphinganine are metabolized into dihydroceramides and cerebrosides by the enzymes of complex sphingolipid synthesis.

Type
Pathology
Copyright
Copyright © Microscopy Society of America 1997

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References

1.Bibel, D.J.et al., Acta Dermatology and Venereology, 73(1993)407.Google Scholar
2.Wertz, P.W.et al., Journal of Investigative Dermatology, 94(1990)159.10.1111/1523-1747.ep12874122CrossRefGoogle Scholar
3.Bibel., D.J.et al., Journal of Investigative Dermatology, 98(1992)269.10.1111/1523-1747.ep12497842CrossRefGoogle Scholar
4.Aaronson, L.R.et al., Molecular Biology of the Cell, 4(1993)233a.Google Scholar
5.Sternberg, S., Science, 266(1994)1632.10.1126/science.7702654CrossRefGoogle Scholar