| Literature DB >> 11313408 |
G A Kingsbury1, L A Feeney, Y Nong, S A Calandra, C J Murphy, J M Corcoran, Y Wang, M R Prabhu Das, S J Busfield, C C Fraser, J L Villeval.
Abstract
The CD2 family is a growing family of Ig domain-containing cell surface proteins involved in lymphocyte activation. Here we describe the cloning and expression analysis of a novel member of this family, B lymphocyte activator macrophage expressed (BLAME). BLAME shares the structural features of the CD2 family containing an IgV and IgC2 domain and clusters with the other family members on chromosome 1q21. Quantitative PCR and Northern blot analysis show BLAME to be expressed in lymphoid tissue and, more specifically, in some populations of professional APCs, activated monocytes, and DCS: Retroviral forced expression of BLAME in hematopoietic cells of transplanted mice showed an increase in B1 cells in the peripheral blood, spleen, lymph nodes, and, most strikingly, in the peritoneal cavity. These cells do not express CD5 and are CD23(low)Mac1(low), characteristics of the B1b subset. BLAME may therefore play a role in B lineage commitment and/or modulation of signal through the B cell receptor.Entities:
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Year: 2001 PMID： 11313408 DOI： 10.4049/jimmunol.166.9.5675
Source DB: PubMed Journal: J Immunol ISSN： 0022-1767 Impact factor: 5.422