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Molecular cloning and characterization of cDNA encoding CD11b of cattle |
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| Authors: | Gopinath Raju S Ambagala Aruna P N Ambagala Thanuja C Liu Weiguo Srikumaran Subramaniam |
| Institution: | aDepartment of Veterinary and Biomedical Sciences, University of Nebraska–Lincoln, Lincoln, NE 68583-0905, USA bDepartment of Veterinary Microbiology and Pathology, College of Veterinary Medicine, Washington State University, 402 Bustad Hall, P.O. Box 647040, Pullman, WA 99164-7040, USA |
| Abstract: | CD18, the common β subunit of β2-integrins, associates with four distinct  chains to give rise to four different β2-integrins: CD11a/CD18 (LFA-1), CD11b/CD18 (Mac-1), CD11c/CD18 (CR4), and CD11d/CD18. Previously, we and others showed that CD18 of LFA-1 serves as a receptor for Mannheimia haemolytica leukotoxin (Lkt). Level of expression of Mac-1 is higher than that of LFA-1 and other β2-integrins on polymorphonuclear leukocytes (PMNs), which constitute the leukocyte subset most susceptible to Lkt. Hence, it is likely that CD18 of Mac-1 also mediates Lkt-induced cytolysis. Co-expression of CD11b and CD18 of cattle on Lkt-resistant cells is necessary to irrefutably demonstrate the role of Mac-1 in Lkt-induced cytolysis. This approach is hindered by lack of availability of complete sequence of cattle CD11b. Therefore, in this study, we cloned and sequenced the full length cDNA encoding cattle CD11b. The 3459 bp cDNA of cattle CD11b encodes a polypeptide of 1152 amino acids. The deduced amino acid sequence of CD11b of cattle exhibits 75% identity to that of humans and chimpanzees, 74% identity to that of dogs, and 70% identity to that of mice and rats. Availability of cattle CD11b cDNA should facilitate the elucidation of Lkt-receptor interactions in cattle and other species. |
| Keywords: | Cattle CD11b cDNA Cloning Sequencing |
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