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14. THEMIS increases TCR signaling in CD4+CD8+ thymocytes by inhibiting the activity of the tyrosine phosphatase SHP1.

Author

Choi, Seeyoung, Lee, Jan, Hatzihristidis, Teri, Gaud, Guillaume, Dutta, Avik, Arya, Awadhesh, Clubb, Lauren M., Stamos, Daniel B., Markovics, Adrienn, Mikecz, Katalin, and Love, Paul E.

Subjects
THYMOCYTES, T cells, KNOCKOUT mice, T cell receptors
Abstract

The T cell lineage–restricted protein THEMIS plays a critical role in T cell development at the positive selection stage. In the SHP1 activation model, THEMIS is proposed to enhance the activity of the tyrosine phosphatase SHP1 (encoded by Ptpn6), thereby dampening T cell antigen receptor (TCR) signaling and preventing the inappropriate negative selection of CD4+CD8+ thymocytes by positively selecting ligands. In contrast, in the SHP1 inhibition model, THEMIS is proposed to suppress SHP1 activity, rendering CD4+CD8+ thymocytes more sensitive to TCR signaling initiated by low-affinity ligands to promote positive selection. We sought to resolve the controversy regarding the molecular function of THEMIS. We found that the defect in positive selection in Themis−/− thymocytes was ameliorated by pharmacologic inhibition of SHP1 or by deletion of Ptpn6 and was exacerbated by SHP1 overexpression. Moreover, overexpression of SHP1 phenocopied the Themis−/− developmental defect, whereas deletion of Ptpn6, Ptpn11 (encoding SHP2), or both did not result in a phenotype resembling that of Themis deficiency. Last, we found that thymocyte negative selection was not enhanced but was instead impaired in the absence of THEMIS. Together, these results provide evidence favoring the SHP1 inhibition model, supporting a mechanism whereby THEMIS functions to enhance the sensitivity of CD4+CD8+ thymocytes to TCR signaling, enabling positive selection by low-affinity, self-ligand–TCR interactions. THEMIS shuts down SHP1 in thymocytes: In the thymus, the exposure of CD4 and CD8 double-positive (DP) thymocytes to self-peptide ligands that stimulate the T cell receptor (TCR) determines their fate. Insufficient TCR signaling results in death by neglect; excessive signaling leads to death by apoptosis to remove self-reactive cells; and sufficient signaling enables the positive selection of the thymocytes into CD4 or CD8 single-positive T cells. Mice deficient in the protein THEMIS exhibit failed thymocyte positive selection. Choi et al. showed that knockout of the inhibitory tyrosine phosphatase SHP1 reversed this defect in Themis knockout mice. Consistent with a model in which THEMIS inhibits SHP1 activity, overexpression of SHP1 phenocopied the effect of loss of THEMIS. In addition, DP thymocyte negative selection was impaired in the absence of THEMIS. Together, these findings suggest that THEMIS inhibits SHP1 in DP thymocytes to enhance their sensitivity to TCR stimulation by self-peptides. —JFF [ABSTRACT FROM AUTHOR]

Published
2023
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24. Additional file 4 of Regulation of autoimmune arthritis by the SHP-1 tyrosine phosphatase

Author

Markovics, Adrienn, Toth, Daniel M., Glant, Tibor T., and Mikecz, Katalin

Abstract

Additional file 4. Serum anti-human PG antibody levels in PG-immunized and SHP-1 activator-treated or untreated mice. Anti-human PG antibody content was measured in the sera of PG-immunized mice. WT mice underwent vehicle or regorafenib treatment, while Shp1-Tg+/- mice did not receive treatment. Serum antibody titers are expressed as optical density (mean±SEM, n=5/group, one-way ANOVA).

Published
2020
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25. Additional file 3 of Regulation of autoimmune arthritis by the SHP-1 tyrosine phosphatase

Author

Markovics, Adrienn, Toth, Daniel M., Glant, Tibor T., and Mikecz, Katalin

Abstract

Additional file 3 Anti-human PG antibody levels in the sera of naïve and PG-immunized mice. Anti-human PG IgG antibody contents were measured in the sera of naïve and PG-immunized WT and the 2 genotypes of Shp1-Tg mice and expressed as optical density at 450 nm (mean±SEM, n=5-10/group, one-way ANOVA).

Published
2020
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41. TSG-6: a new regulator of bone remodeling

Author

Day, Anthony J., Mahoney, David J., Mikecz, Katalin, Mabilleau, Guillaume, Athanasou, Nick A., Ali, Tariq, Milner, Caroline M., and Sabokbar, Afsie

Published
2008

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