| Literature DB >> 11114375 |
A Kumanogoh1, C Watanabe, I Lee, X Wang, W Shi, H Araki, H Hirata, K Iwahori, J Uchida, T Yasui, M Matsumoto, K Yoshida, H Yakura, C Pan, J R Parnes, H Kikutani.
Abstract
We have identified the lymphocyte semaphorin CD100/Sema4D as a CD40-inducible molecule by subtractive cDNA cloning. CD100 stimulation significantly enhanced the effects of CD40 on B cell responses. Administration of soluble CD100 markedly accelerated in vivo antigen-specific antibody responses. CD100 receptors with different binding affinities were detected on renal tubular cells (K(d) = approximately 1 x 10(-9)M) and lymphocytes (K(d) = approximately 3 x 10(-7)M). Expression cloning revealed that the CD100 receptor on lymphocytes is CD72, a negative regulator of B cell responsiveness. CD72 thus represents a novel class of semaphorin receptors. CD100 stimulation induced tyrosine dephosphorylation of CD72 and dissociation of SHP-1 from CD72. Our findings indicate that CD100 plays a critical role in immune responses by the novel mechanism of turning off negative signaling by CD72.Entities:
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Year: 2000 PMID: 11114375 DOI: 10.1016/s1074-7613(00)00062-5
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745