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Department of Molecular Microbiology and Immunology, School of Medicine, and
Department of Veterinary Pathobiology, College of Veterinary Medicine, University of Missouri, Columbia, MO 65211
CD5, a type I glycoprotein expressed by T cells and a subset of B
cells, is thought to play a significant role in modulating Ag receptor
signaling. Previously, our laboratory has shown that bovine B cells are
induced to express this key regulatory molecule upon Ag receptor
cross-linking. To date, a ligand has not been described for bovine CD5.
Given the importance ligand binding presumably plays in the functioning
of CD5 on this B cell subset and on T cells, we sought to characterize
the ligand for this protein using a bovine CD5-human IgG1 (CD5Ig)
fusion protein produced by both mammalian and yeast cells. As
determined by CD5Ig binding, expression of this ligand is negative to
low on freshly isolated lymphocytes, with low-density expression being
limited to activated B cells. Activation with LPS, PMA, and calcium
ionophore, or ligation of CD40 alone or in combination with
anti-IgM, resulted in B cell-specific expression of this ligand.
Interestingly, activation through B cell Ag receptor cross-linking
alone, although able to induce CD5 expression, did not result in
expression of CD5 ligand (CD5L). In addition, we demonstrate a
functional role for CD5L as a costimulatory molecule that augments
CD40L-stimulated B cell proliferation. Finally, immunoprecipitation
with CD5Ig suggests that the ligand characterized in this study has a
molecular mass of
200 kDa. The data reported herein, as well as
future studies aimed at further characterizing this newly identified
bovine CD5L, will undoubtedly aid in understanding the role that the
CD5-CD5L interaction plays in immune responses.
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