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Porcine alveolar macrophage Mac‐1 (CD11b/CD18) adhesion molecule expression
Author(s) -
Lee JongKeuk,
Schook Lawrence B.,
Rutherford Mark S.
Publication year - 1996
Publication title -
xenotransplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.052
H-Index - 61
eISSN - 1399-3089
pISSN - 0908-665X
DOI - 10.1111/j.1399-3089.1996.tb00152.x
Subject(s) - microbiology and biotechnology , integrin alpha m , biology , monoclonal antibody , complementary dna , antibody , spleen , western blot , epitope , cd18 , flow cytometry , immunology , biochemistry , gene
The adhesion molecule Mac‐1 plays an important role during leukocyte recruitment into inflammatory sites and also serves as a complement receptor type 3 (CR3). Mac‐1 is a noncovalent heterodimer consisting of an α‐chain (CD11b) and a β‐chain (CD 18). We report the cloning and sequencing (GenBank accession number U40072) of the porcine CD 11b cDNA using the reverse transcriptase‐polymerase chain reaction (RT‐PCR). Porcine CD 11b cDNA and deduced amino acid sequences demonstrated 84% and 80% sequence identity, respectively, with human CD11b. The 4.7 kb porcine CD11b transcript was also similar to the size of the human CD11b transcript. Northern blot analyses detected CD11b transcripts in spleen cells and peripheral blood leukocytes, but not in lung lavage cells. In contrast to Northern blot results, 72% of freshly isolated alveolar macrophages stained positive using a cross‐reactive anti‐human CD11b antibody (TMG6–5). Compared to spleen and peripheral blood cells, alveolar macrophages expressed the highest levels of CD 18 mRNA. Using anti‐CD 18 monoclonal antibodies which cross‐react with porcine CD 18, two different porcine CD 18 epitopes were identified by flow cytometric antibody competition assays. However, the majority of the anti‐CD 18 antibodies tested competed for the same CD 18 epitope. Mac‐1 expression in porcine alveolar macrophages was not altered at either the mRNA or surface expression level by inflammatory stimuli, including fMLP, PMA, LPS, hIL‐1α, hIL‐6, hTNF‐α, and hIFN‐γ.