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Open Access Research article

Evolution of the CD163 family and its relationship to the bovine gamma delta T cell co-receptor WC1

Carolyn TA Herzig1, Ray W Waters2, Cynthia L Baldwin1 and Janice C Telfer1*

Author Affiliations

1 University of Massachusetts Amherst, Department of Veterinary and Animal Sciences, Paige Laboratory, Amherst, MA 01003, USA

2 National Animal Diseases Center, USDA-ARS, Ames, Iowa, 50010, USA

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BMC Evolutionary Biology 2010, 10:181  doi:10.1186/1471-2148-10-181

Published: 15 June 2010

Abstract

Background

The scavenger receptor cysteine rich (SRCR) domain is an ancient and conserved protein domain. CD163 and WC1 molecules are classed together as group B SRCR superfamily members, along with Spα, CD5 and CD6, all of which are expressed by immune system cells. There are three known types of CD163 molecules in mammals, CD163A (M130, coded for by CD163), CD163b (M160, coded for by CD163L1) and CD163c-α (CD163L1 or SCART), while their nearest relative, WC1, is encoded by a multigene family so far identified in the artiodactyl species of cattle, sheep, and pigs.

Results

We annotated the bovine genome and identified genes coding for bovine CD163A and CD163c-α but found no evidence for CD163b. Bovine CD163A is widely expressed in immune cells, whereas CD163c-α transcripts are enriched in the WC1+ γδ T cell population. Phylogenetic analyses of the CD163 family genes and WC1 showed that CD163c-α is most closely related to WC1 and that chicken and platypus have WC1 orthologous genes, previously classified as among their CD163 genes.

Conclusion

Since it has been shown that WC1 plays an important role in the regulation of γδ T cell responses in cattle, which, like chickens, have a high percentage of γδ T cells in their peripheral blood, CD163c-α may play a similar role, especially in species lacking WC1 genes. Our results suggest that gene duplications resulted in the expansion of CD163c-α-like and WC1-like molecules. This expanded repertoire was retained by species known as "γδ T cell high", but homologous SRCR molecules were maintained by all mammals.