| First Author | Nagasu A | Year | 2019 |
| Journal | Cells | Volume | 8 |
| Issue | 5 | PubMed ID | 31052273 |
| Mgi Jnum | J:289728 | Mgi Id | MGI:6434633 |
| Doi | 10.3390/cells8050402 | Citation | Nagasu A, et al. (2019) Sh3bp2 Gain-Of-Function Mutation Ameliorates Lupus Phenotypes in B6.MRL-Fas(lpr) Mice. Cells 8(5):402 |
| abstractText | SH3 domain-binding protein 2 (SH3BP2) is an adaptor protein that is predominantly expressed in immune cells, and it regulates intracellular signaling. We had previously reported that a gain-of-function mutation in SH3BP2 exacerbates inflammation and bone loss in murine arthritis models. Here, we explored the involvement of SH3BP2 in a lupus model. Sh3bp2 gain-of-function (P416R knock-in; Sh3bp2(KI/+)) mice and lupus-prone B6.MRL-Fas(lpr) mice were crossed to yield double-mutant (Sh3bp2(KI/+)Fas(lpr/lpr)) mice. We monitored survival rates and proteinuria up to 48 weeks of age and assessed renal damage and serum anti-double-stranded DNA antibody levels. Additionally, we analyzed B and T cell subsets in lymphoid tissues by flow cytometry and determined the expression of apoptosis-related molecules in lymph nodes. Sh3bp2 gain-of-function mutation alleviated the poor survival rate, proteinuria, and glomerulosclerosis and significantly reduced serum anti-dsDNA antibody levels in Sh3bp2(KI/+)Fas(lpr/lpr) mice. Additionally, B220(+)CD4(-)CD8(-) T cell population in lymph nodes was decreased in Sh3bp2(KI/+)Fas(lpr/lpr) mice, which is possibly associated with the observed increase in cleaved caspase-3 and tumor necrosis factor levels. Sh3bp2 gain-of-function mutation ameliorated clinical and immunological phenotypes in lupus-prone mice. Our findings offer better insight into the unique immunopathological roles of SH3BP2 in autoimmune diseases. |
