Lymphoid-Specific Tyrosine Phosphatase (Lyp): A Potential Drug Target For Treatment of Autoimmune Diseases

被引:12
作者
Du, Jintong [1 ,2 ]
Qiao, Yu [2 ]
Sun, Lele [2 ]
Wang, Xiuwen [1 ]
机构
[1] Shandong Univ, Qilu Hosp, Dept Chemotherapy, Jinan 250012, Shandong, Peoples R China
[2] Shandong Univ, Dept Pharmaceut Sci, Jinan 250012, Shandong, Peoples R China
关键词
Autoimmune diseases; lymphoid-tyrosine phosphatase; Lyp; PTPs; inhibitor; REGULATORY T-CELLS; SINGLE-NUCLEOTIDE POLYMORPHISM; JUVENILE IDIOPATHIC ARTHRITIS; PTPN22 SPLICE FORMS; RHEUMATOID-ARTHRITIS; R620W POLYMORPHISM; GENETIC ASSOCIATION; RISK-FACTOR; SIGNIFICANTLY DIFFERENT; FUNCTIONAL VARIANT;
D O I
10.2174/13894501113146660236
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Lymphoid-tyrosine phosphatase (Lyp), encoded by the PTPN22 gene, is a member of the protein tyrosine phosphatase family enzymes. Human genetics studies have shown that a single-nucleotide polymorphism in PTPN22 is often mutated in patients suffering from autoimmune diseases such as type 1 diabetes, rheumatoid arthritis, and systemic lupus erythematosis. Because of its critical role in the regulation of T-cell Receptor (TCR) signaling pathways, Lyp recently emerged as a candidate target for therapy of autoimmune diseases. Herein, we review the structure and splice isoforms of Lyp, the biochemistry of the disease-predisposing allele, discuss the function of the phosphatase in TCR signaling and the association with human autoimmune diseases. Especially, we summarized recent progress in the development of Lyp inhibitors, intending to provide a basis for the Lyp-based treatment of autoimmunity. Moreover, the emphasis and direction for future study of Lyp in autoimmune diseases were prospected.
引用
收藏
页码:335 / 346
页数:12
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