Neuraminidases 3 and 4 regulate neuronal function by catabolizing brain gangliosides

Xuefang Pan, Camila De Britto Pará De Aragão, Juan P. Velasco-Martín, David A. Priestman, Harry Y. Wu, Kohta Takahashi, Kazunori Yamaguchi, Luisella Sturiale, Domenico Garozzo, Frances M. Platt,

The FASEB Journal · 2017 · 61 citations · 26 references

Concepts

Abstract

ABSTRACT Gangliosides (sialylated glycolipids) play an essential role in the CNS by regulating recognition and signaling in neurons. Metabolic blocks in processing and catabolism of gangliosides result in the development of severe neurologic disorders, including gangliosidoses manifesting with neurodegeneration and neuroinflammation. We demonstrate that 2 mammalian enzymes, neuraminidases 3 and 4, play important roles in catabolic processing of brain gangliosides by cleaving terminal sialic acid residues in their glycan chains. In neuraminidase 3 and 4 double‐knockout mice, G M3 ganglioside is stored in microglia, vascular pericytes, and neurons, causing micro‐ and astrogliosis, neuroinflammation, accumulation of lipofuscin bodies, and memory loss, whereas their cortical and hippocampal neurons have lower rate of neuritogenesis in vitro. Double‐knockout mice also have reduced levels of G M1 ganglioside and myelin in neuronal axons. Furthermore, neuraminidase 3 deficiency drastically increased storage of G M2 in the brain tissues of an asymptomatic mouse model of Tay‐Sachs disease, a severe human gangliosidosis, indicating that this enzyme is responsible for the metabolic bypass of β‐hexosaminidase A deficiency. Together, our results provide the first in vivo evidence that neuraminidases 3 and 4 have important roles in CNS function by catabolizing gangliosides and preventing their storage in lipofuscin bodies.—Pan, X., De Britto Pará De Aragão, C., Velasco‐Martin, J. P., Priestman, D. A., Wu, H. Y., Takahashi, K., Yamaguchi, K., Sturiale, L., Garozzo, D., Platt, F. M., Lamarche‐Vane, N., Morales, C. R., Miyagi, T., Pshezhetsky, A. V. Neuraminidases 3 and 4 regulate neuronal function by catabolizing brain gangliosides. FASEB J . 31, 3467–3483 (2017). www.fasebj.org

References

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