Novel Binding Site for Src Homology 2-containing Protein-tyrosine Phosphatase-1 in CD22 Activated by B Lymphocyte Stimulation with Antigen
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference33 articles.
1. The role of CD22 and other inhibitory co-receptors in B-cell activation
2. Molecular interactions regulate BCR signal inhibition by CD22 and CD72
3. Definition of the Sites of Interaction between the Protein Tyrosine Phosphatase SHP-1 and CD22
4. CD22 associates with protein tyrosine phosphatase 1C, Syk, and phospholipase C-gamma(1) upon B cell activation.
5. CD22 Forms a Quaternary Complex with SHIP, Grb2, and Shc
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1. Neu5Gc-mediated high-affinity interaction is dispensable for CD22 cis-ligands to regulate B cell signaling;Journal of Biological Chemistry;2024-09
2. The ligand interactions of B cell Siglecs are involved in the prevention of autoimmunity to sialylated self-antigens and in the quality control of signaling-competent B cells;International Immunology;2023-07-28
3. The inhibitory coreceptor CD22 restores B cell signaling by developmentally regulatingCd45−/−immunodeficient B cells;Science Signaling;2022-03
4. The Protein Tyrosine Phosphatase SHP-1 (PTPN6) but Not CD45 (PTPRC) Is Essential for the Ligand-Mediated Regulation of CD22 in BCR-Ligated B Cells;The Journal of Immunology;2021-05-14
5. Besides an ITIM/SHP-1-dependent pathway, CD22 collaborates with Grb2 and plasma membrane calcium-ATPase in an ITIM/SHP-1-independent pathway of attenuation of Ca2+i signal in B cells;Oncotarget;2016-06-02
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