Ablation of lipocalin-2 reduces neuroinflammation in a mouse model of Krabbe disease

Sci Rep. 2024 Dec 30;14(1):31822. doi: 10.1038/s41598-024-82927-1.

Abstract

Lipocalin-2 (LCN2) is an acute-phase secretory molecule significantly upregulated in various neuroinflammatory and demyelinating conditions. Krabbe disease (KD) is a neurodegenerative lysosomal disorder caused by a galactosylceramidase (GALC) deficiency, accumulating cytotoxic psychosine in nervous systems, and subsequent neuroinflammation. Here, we show that LCN2 is highly overexpressed in GALC-deficient astrocytes. To further understand if the elevated LCN2 is critical for KD progression, we globally deleted Lcn2 in the Galc-knockout (KO) mouse model. Interestingly, the Galc and Lcn2 double KO mice showed dramatically reduced neuroinflammation including gliosis. Pro-inflammatory cytokines such as TNF-α, MMP3, and MCP-1 were significantly downregulated in the brain of the double KO mice compared to Galc-KO. In addition, the ablation of Lcn2 marginally increased the survival and attenuated disease progression in Galc-KO mice. However, the accumulation of psychosine was not altered in the brain by LCN2 deficiency. Our findings suggest that the upregulation of LCN2 is crucial for the aggravation of neuroinflammation in a mouse model of Krabbe disease.

Keywords: Galactosylceramidase; Gliosis; Globoid cell leukodystrophy; Krabbe disease; Lipocalin-2; Lysosomal storage disorder; Neuroinflammation; Psychosine.

MeSH terms

  • Animals
  • Astrocytes* / metabolism
  • Astrocytes* / pathology
  • Brain / metabolism
  • Brain / pathology
  • Chemokine CCL2 / genetics
  • Chemokine CCL2 / metabolism
  • Disease Models, Animal*
  • Galactosylceramidase / genetics
  • Galactosylceramidase / metabolism
  • Gliosis / metabolism
  • Gliosis / pathology
  • Leukodystrophy, Globoid Cell* / genetics
  • Leukodystrophy, Globoid Cell* / metabolism
  • Leukodystrophy, Globoid Cell* / pathology
  • Lipocalin-2* / genetics
  • Lipocalin-2* / metabolism
  • Matrix Metalloproteinase 3
  • Mice
  • Mice, Knockout*
  • Neuroinflammatory Diseases* / metabolism
  • Neuroinflammatory Diseases* / pathology
  • Psychosine / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Lipocalin-2
  • Lcn2 protein, mouse
  • Galactosylceramidase
  • Tumor Necrosis Factor-alpha
  • Chemokine CCL2
  • Mmp3 protein, mouse
  • Psychosine
  • Ccl2 protein, mouse
  • Matrix Metalloproteinase 3