Sialidase neu4 deficiency is associated with neuroinflammation in mice

• Published in: Glycoconjugate journal Vol. 38; no. 6; pp. 649 - 667
• Main Authors: Timur, Zehra Kevser, Inci, Orhan Kerim, Demir, Secil Akyildiz, Seyrantepe, Volkan
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.12.2021; Springer Nature B.V
• Subjects: Acids; Animals; Apoptosis; Biochemistry; Biomedical and Life Sciences; Cerebellum; Chemokines; Cytokines; Disease; Ganglioside GM1; Gangliosides; Gangliosides - metabolism; Gliosis; Glycolipids; Glycoproteins; Inflammation; Life Sciences; Lysosomes - metabolism; Mice; Morphology; Mucolipidoses - metabolism; Musculoskeletal system; Nervous system; Neuraminidase - chemistry; Neuraminidase - metabolism; Neuroinflammatory Diseases; Oligosaccharides; Original Article; Pathology; Spleen; Substrate Specificity; Neuroinflammation; Neu4; Behavior; Ganglioside; Sialidase
• ISSN: 0282-0080; 1573-4986; 1573-4986
• DOI: 10.1007/s10719-021-10017-9

Sialidases catalyze the removal of sialic acid residues from glycoproteins, oligosaccharides, and sialylated glycolipids. Sialidase Neu4 is in the lysosome and has broad substrate specificity. Previously generated Neu4-/- mice were viable, fertile and lacked gross morphological abnormalities, but displayed a marked vacuolization and lysosomal storage in lung and spleen cells. In addition, we showed that there is an increased level of GD1a ganglioside and a markedly decreased level of GM1 ganglioside in the brain of Neu4-/- mice. In this study, we further explored whether sialidase Neu4 deficiency causes neuroinflammation. We demostrated that elevated level of GD1a and GT1b is associated with an increased level of LAMP1-positive lysosomal vesicles and Tunel-positive neurons correlated with alterations in the expression of cytokines and chemokines in adult Neu4-/- mice. Astrogliosis and microgliosis were also significantly enhanced in the hippocampus, and cerebellum. These changes in brain immunity were accompanied by motor impairment in these mice. Our results indicate that sialidase Neu4 is a novel mediator of an inflammatory response in the mouse brain due to the altered catabolism of gangliosides.