Neu5Gc-mediated high-affinity interaction is dispensable for CD22 cis-ligands to regulate B cell signaling-Reference-Cited by-同舟云学术

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Neu5Gc-mediated high-affinity interaction is dispensable for CD22 cis-ligands to regulate B cell signaling

Published:2024-09 Issue:9 Volume:300 Page:107630
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Akatsu Chizuru,Naito-Matsui Yuko,Abdu-Allah Hajjaj H.M.^ORCID,Imamura Akihiro^ORCID,Long Wang,Ishida Hideharu^ORCID,Takematsu Hiromu^ORCID,Tsubata Takeshi^ORCID

Funder

University of Toyama

University of California, Santa Barbara

Japan Society for the Promotion of Science

Publisher

Elsevier BV

Reference41 articles.

1. CD22 and Siglec-G regulate inhibition of B-cell signaling by sialic acid ligand binding and control B-cell tolerance;Nitschke;Glycobiology,2014

2. Siglec cis-ligands and their roles in the immune system;Tsubata;Glycobiology,2023

3. Novel binding site for Src homology 2-containing protein-tyrosine phosphatase-1 in CD22 activated by B lymphocyte stimulation with antigen;Zhu;J. Biol. Chem.,2008

4. The oligosaccharide binding specificities of CD22 beta, a sialic acid-specific lectin of B cells;Powell;J. Biol. Chem.,1994

5. Sialoadhesin, myelin-associated glycoprotein and CD22 define a new family of sialic acid-dependent adhesion molecules of the immunoglobulin superfamily;Kelm;Curr. Biol.,1994

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