Comprehensive Expression Profiles of Genes for Protein Tyrosine Phosphatases in Immune Cells

被引:49
作者
Arimura, Yutaka [1 ]
Yagi, Junji [1 ]
机构
[1] Tokyo Womens Med Univ, Sch Med, Shinjuku Ku, Tokyo 1628666, Japan
关键词
DUAL-SPECIFICITY PHOSPHATASE; KINASE; CD45; MOUSE; ASSOCIATION; ACTIVATION; PTPN22; TRANSCRIPTOME; POLYMORPHISM; MUTATIONS;
D O I
10.1126/scisignal.2000966
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The phosphorylation and dephosphorylation of signaling molecules play a crucial role in various cellular processes, including immune responses. To date, the global expression profile of protein tyrosine phosphatases (PTPs) in various immune cells has not been described. With the RefDIC (Reference Genomics Database of Immune Cells) database compiled by RIKEN (Rikagaku Kenkyusho), we examined the expression patterns of PTP-encoding genes in mice and identified between 57 and 64 PTP-encoding genes (depending on cutoff values) that were commonly expressed in immune cells. Cells of different lineages contained additional, unique PTP-encoding genes, which resulted in a total of 58 to 76 genes. Compared with cells from nonimmune tissues, immune cells exhibited enhanced expression of the genes encoding 8 PTP-encoding genes, including Ptprc, Ptpn6, and Ptpn22, but had barely detectable expression of 11 PTP-encoding genes, including Ptprd and Tns1. Each immune cell lineage had between 2 and 18 PTP-encoding genes expressed at relatively high or low extents relative to the average expression among immune cells; for example, Ptprj in B cells, Dusp3 in macrophages, Ptpro in dendritic cells, and Ptprg in mast cells. These PTPs potentially play important roles in each cell lineage, and our analysis provides insight for future functional studies.
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页数:10
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