GLI1 facilitates rheumatoid arthritis by collaborative regulation of DNA methyltransferases

Ge, G.; Guo, Q.; Zhou, Y.; Li, W.; Zhang, W.; Bai, J.; Wang, Q.; Tao, H.; Wang, W.; Wang, Z.; Gan, M.; Xu, Y.; Yang, H.; Li, B.; Geng, D.

doi:10.1101/2023.02.07.527456

bioRxiv · 10.1101/2023.02.07.527456

GLI1 facilitates rheumatoid arthritis by collaborative regulation of DNA methyltransferases

Ge, G.·Guo, Q.·Zhou, Y.·Li, W.·Zhang, W.·Bai, J.·Wang, Q.·Tao, H.·Wang, W.·Wang, Z.·Gan, M.·Xu, Y.·Yang, H.·Li, B.·Geng, D.

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Abstract

Rheumatoid arthritis (RA) is characterized by joint synovitis and bone destruction, the etiology of which remains to be explored. Overactivation of M1 macrophages and osteoclasts has been thought a direct cause of joint inflammation and bone destruction. Glioma-associated oncogene homolog 1 (GLI1) has been revealed to be closely linked to bone metabolism. In this study, GLI1-expression in synovial tissue of RA patients showed to be positively correlated with RA-related scores and was highly expressed in collagen-induced arthritis (CIA) mouse articular macrophage-like cells. The decreased expression and inhibition of nuclear transfer of GLI1 downregulated macrophage M1 polarization and osteoclast activation, the effect of which was achieved by modulation of DNA methyltransferases (DNMTs) via transcriptional regulation and protein interaction ways. By pharmacological inhibition of GLI1, the proportion of proinflammatory macrophages and the number of osteoclasts were significantly reduced, and the joint inflammatory response and bone destruction in CIA mice were alleviated. This study clarified the mechanism of GLI1 in macrophage phenotypic changes and activation of osteoclasts, suggesting potential applications of GLI1 inhibitor in the clinical treatment of RA.

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Ge, G., Guo, Q., Zhou, Y., Li, W., Zhang, W., Bai, J., Wang, Q., Tao, H., Wang, W., Wang, Z., Gan, M., Xu, Y., Yang, H., Li, B., Geng, D.. 2023-02-07. GLI1 facilitates rheumatoid arthritis by collaborative regulation of DNA methyltransferases. https://doi.org/10.1101/2023.02.07.527456

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