Differential expression of CD22 (Lyb8) on murine B cells |
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Authors: | Erickson, Loren D. Tygrett, Lorraine T. Bhatia, Sudershan K. Grabstein, Kenneth H. Waldschmidt, Thomas J. |
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Affiliation: | 1 Departments of Pathology, University of Iowa College of Medicine Iowa City, IA 52242, USA 2 Department of immunology Graduate Program, University of Iowa College of Medicine Iowa City, IA 52242, USA 3 Corixa Corp. Seattle, WA 98101, USA |
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Abstract: | Previous studies have established the distribution, biochemistryand functional attributes of human CD22, a B cell-restrictedglycoprotein. Recently, molecular cloning of the murine CD22equivalent revealed this molecule to be the same as the previouslydescribed Lyb8 alloantigen. Using the anti-Lyb8 mAb Cy34.1.2,the present report documents the expression patterns of CD22within the murine B cell compartment. The results demonstratethat in the bone marrow, murine CD22 is absent on the surfaceof pro-B cells, pre-B cells and newly emerging lgM+ B cells.CD22 is present at a low density on immature IgMhi B cells andfully expressed on mature recirculating B cells. In the periphery,murine CD22 is expressed at mature levels on all B cell subsetsincluding follicular, marginal zone, B1 and switched B cells.Further studies showed CD22 to be retained on activated murineB cells for extended periods. Finally, in combination with CD23and heat stable antigen, CD22 can be used to delineate the immaturesplenic B cells, and distinguish them from follicular and marginalzone cells. Together, the results demonstrate murine CD22 tobe a useful pan marker for all mature B cell subsets. |
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Keywords: | B cell B lymphocytes heat stable antigen |
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