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Mouse macrophage beta subunit (CD11b) cDNA for the CR3 complement receptor/Mac-1 antigen
D L Zeger1, N Osman, M Hennings
1Department of Biological Sciences, University of California, Santa Barbara 93106.
Immunogenetics
|January 1, 1990
Summary
Researchers cloned and sequenced the mouse Mac-1 subunit (CD11b), a key leukocyte cell adhesion receptor. This finding provides insights into conserved functions in immune cell interactions and phagocytosis.
Area of Science:
- Immunology
- Molecular Biology
- Cell Biology
Background:
- Leukocyte cell adhesion receptors, including the LFA-1/Mac-1/p150,95 group (integrin beta 2), play critical roles in immune responses.
- The Mac-1 subunit (CD11b) is a component of macrophage activation antigen 1 (Mac-1), also known as complement receptor type 3 (CR3).
Purpose of the Study:
- To clone and sequence the complementary DNA (cDNA) for the common beta Mac-1 subunit (CD11b) in mice.
- To analyze the structural characteristics and evolutionary conservation of the mouse Mac-1 subunit.
Main Methods:
- Isolation of clones from cDNA libraries derived from J774 macrophage and WEHI-3B myelomonocytic tumor cells.
- Sequencing of the 2422 base pair (bp) cDNA to determine the protein structure and identify conserved domains.
Main Results:
- The mouse beta Mac-1 subunit cDNA sequence was obtained, coding for a 771 amino acid protein with distinct functional domains.
- High sequence identity (81%) was observed between the mouse and human beta Mac-1 subunits, particularly in the transmembrane and cytoplasmic domains.
- Conserved N-linked glycosylation sites and cysteine residues indicate conserved structural motifs characteristic of integrin beta subunits.
Conclusions:
- The cloning and sequencing of the mouse beta Mac-1 subunit provide a molecular basis for understanding its role in cell adhesion and immune functions.
- Highly conserved transmembrane and cytoplasmic domains suggest conserved mechanisms in Mac-1-mediated processes, such as iC3b-triggered phagocytosis.
- The findings highlight the evolutionary conservation of integrin beta subunit structure and function.