| First Author | Magnusen AF | Year | 2021 |
| Journal | Int J Mol Sci | Volume | 22 |
| Issue | 23 | PubMed ID | 34884512 |
| Mgi Jnum | J:328129 | Mgi Id | MGI:6833571 |
| Doi | 10.3390/ijms222312712 | Citation | Magnusen AF, et al. (2021) C-X-C Motif Chemokine Ligand 9 and Its CXCR3 Receptor Are the Salt and Pepper for T Cells Trafficking in a Mouse Model of Gaucher Disease. Int J Mol Sci 22(23) |
| abstractText | Gaucher disease is a lysosomal storage disease, which happens due to mutations in GBA1/Gba1 that encodes the enzyme termed as lysosomal acid beta-glucosidase. The major function of this enzyme is to catalyze glucosylceramide (GC) into glucose and ceramide. The deficiency of this enzyme and resultant abnormal accumulation of GC cause altered function of several of the innate and adaptive immune cells. For example, augmented infiltration of T cells contributes to the increased production of pro-inflammatory cytokines, (e.g., IFNgamma, TNFalpha, IL6, IL12p40, IL12p70, IL23, and IL17A/F). This leads to tissue damage in a genetic mouse model (Gba1(9V/-)) of Gaucher disease. The cellular mechanism(s) by which increased tissue infiltration of T cells occurs in this disease is not fully understood. Here, we delineate role of the CXCR3 receptor and its exogenous C-X-C motif chemokine ligand 9 (CXCL9) in induction of increased tissue recruitment of CD4(+) T and CD8(+) T cells in Gaucher disease. Intracellular FACS staining of macrophages (Mvarphis) and dendritic cells (DCs) from Gba1(9V/-) mice showed elevated production of CXCL9. Purified CD4(+) T cells and the CD8(+) T cells from Gba1(9V/-) mice showed increased expression of CXCR3. Ex vivo and in vivo chemotaxis experiments showed CXCL9 involvement in the recruitment of Gba1(9V/-) T cells. Furthermore, antibody blockade of the CXCL9 receptor (CXCR3) on T cells caused marked reduction in CXCL9- mediated chemotaxis of T cells in Gba1(9V/-) mice. These data implicate abnormalities of the CXCL9-CXCR3 axis leading to enhanced tissue recruitment of T cells in Gaucher disease. Such results provide a rationale for blockade of the CXCL9/CXCR3 axis as potential new therapeutic targets for the treatment of inflammation in Gaucher disease. |
