Characterization of the expression and gene promoter of CD22 in murine B cells

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Abstract
CD22 is a B cell‐restricted surface molecule which may play an important role in interactions between B cells and other cells and in regulating signals through the B cell receptor (BCR) complex. Here we have examined whether the mouse is a suitable in vivo model for studying CD22 functions. In primary and secondary lymphoid organs of adult mice CD22 is on all mature B cells, including resting IgM+IgD+ B cells, IgG+ HSAlo memory B cells, syndecan+ plasma cells and CD5+ B cells, but it is not on immature IgM+IgD− B cells. Biochemical analysis revealed that murine CD22 is associated with the IgM receptor in some, but not all, CD22+ B leukemic and lymphoma cell lines; as with human CD22, murine CD22 is rapidly phosphorylated on tyrosine after ligation of the BCR. In the CD22− murine pro‐B cell line, FEMCL, CD22 expression was inducible by treatment with phorbol 12‐myristate 13‐acetate. A genomic fragment of the cd22b allele containing 1.3 kb 5′ of exon 1 was sequenced in order to identify potential DNA regulatory elements in the CD22 promoter region. Consensus sequences for transcription factor binding sites including PU.1, AP‐1, AP‐2, C/EBP and SP‐1 were present, but no classical TATA elements or initiator motifs were evident at relevant positions. The 1.3‐kb promoter fragment 5′ of exon 1 was sufficient for directing basal promoter activity in B and T cells. There was no significant sequence similarity between the murine and human cd22 gene promoters, although both contain repetitive elements and Sp‐1 and AP1 binding sites. Thus, murine CD22 shares a number of features with human CD22 and the mouse provides a suitable model system for elucidating the function of CD22 in vivo.