Integrin alpha M
Integrin, alpha M (complement component 3 receptor 3 subunit) |
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PDB rendering based on 1bho. |
Available structures |
PDB |
Ortholog search: PDBe, RCSB |
List of PDB id codes |
1A8X, 1BHO, 1BHQ, 1IDN, 1IDO, 1JLM, 1M1U, 1MF7, 1N9Z, 1NA5, 2LKE, 2LKJ, 3Q3G, 3QA3, 4M76
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Identifiers |
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Symbols |
ITGAM ; CD11B; CR3A; MAC-1; MAC1A; MO1A; SLEB6 |
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External IDs |
OMIM: 120980 MGI: 96607 HomoloGene: 526 ChEMBL: 3826 GeneCards: ITGAM Gene |
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RNA expression pattern |
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More reference expression data |
Orthologs |
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Species |
Human |
Mouse |
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Entrez |
3684 |
16409 |
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Ensembl |
ENSG00000169896 |
ENSMUSG00000030786 |
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UniProt |
P11215 |
P05555 |
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RefSeq (mRNA) |
NM_000632 |
NM_001082960 |
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RefSeq (protein) |
NP_000623 |
NP_001076429 |
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Location (UCSC) |
Chr 16: 31.26 – 31.33 Mb |
Chr 7: 128.06 – 128.13 Mb |
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PubMed search |
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Integrin alpha M (ITGAM) is one protein subunit that forms the heterodimeric integrin alpha-M beta-2 (αMβ2) molecule, also known as macrophage-1 antigen (Mac-1) or complement receptor 3 (CR3).[1] ITGAM is also known as CR3A, and cluster of differentiation molecule 11B (CD11B). The second chain of αMβ2 is the common integrin β2 subunit known as CD18, and integrin αMβ2 thus belongs to the β2 subfamily (or leukocyte) integrins.[2]
αMβ2 is expressed on the surface of many leukocytes involved in the innate immune system, including monocytes, granulocytes, macrophages, and natural killer cells.[1] It mediates inflammation by regulating leukocyte adhesion and migration and has been implicated in several immune processes such as phagocytosis, cell-mediated cytotoxicity, chemotaxis and cellular activation.[1] It is involved in the complement system due to its capacity to bind inactivated complement component 3b (iC3b).[3] The ITGAM (alpha) subunit of integrin αMβ2 is directly involved in causing the adhesion and spreading of cells but cannot mediate cellular migration without the presence of the β2 (CD18) subunit.[1]
In genomewide association studies, single nucleotide polymorphisms in ITGAM had the strongest association with systemic lupus erythematosus, with an odds ratio of 1.65 for the T allele of rs9888739 and lupus.[4][5]
In histopathology, immunohistochemistry with antibodies against CD11B is frequently used to identify macrophages and microglia.
See also
References
- 1 2 3 4 Solovjov D, Pluskota E, Plow E (2005). "Distinct roles for the alpha and beta subunits in the functions of integrin alphaMbeta2". J Biol Chem 280 (2): 1336–45. doi:10.1074/jbc.M406968200. PMID 15485828.
- ↑ Larson R, Springer T (1990). "Structure and function of leukocyte integrins". Immunol Rev 114: 181–217. doi:10.1111/j.1600-065X.1990.tb00565.x. PMID 2196220.
- ↑ Arnaout M, Todd R, Dana N, Melamed J, Schlossman S, Colten H (1983). "Inhibition of phagocytosis of complement C3- or immunoglobulin G-coated particles and of C3bi binding by monoclonal antibodies to a monocyte-granulocyte membrane glycoprotein (Mol)". J Clin Invest 72 (1): 171–9. doi:10.1172/JCI110955. PMC 1129172. PMID 6874946.
- ↑ Mary K. Crow (February 28, 2008). "Collaboration, Genetic Associations, and Lupus Erythematosus". N Engl J Med 358 (9): 956–961. doi:10.1056/NEJMe0800096. PMID 18204099.
- ↑ Geoffrey Hom, Robert R. Graham, Barmak Modrek; et al. (February 28, 2008). "Association of Systemic Lupus Erythematosus with C8orf13–BLK and ITGAM–ITGAX". N Engl J Med 358 (9): 900–909. doi:10.1056/NEJMoa0707865. PMID 18204098.
Further reading
PDB gallery |
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| | 1bho: MAC-1 I DOMAIN MAGNESIUM COMPLEX |
| 1bhq: MAC-1 I DOMAIN CADMIUM COMPLEX |
| 1idn: MAC-1 I DOMAIN METAL FREE |
| 1ido: I-DOMAIN FROM INTEGRIN CR3, MG2+ BOUND |
| 1jlm: I-DOMAIN FROM INTEGRIN CR3, MN2+ BOUND |
| 1m1u: AN ISOLEUCINE-BASED ALLOSTERIC SWITCH CONTROLS AFFINITY AND SHAPE SHIFTING IN INTEGRIN CD11B A-DOMAIN |
| 1mf7: INTEGRIN ALPHA M I DOMAIN |
| 1n9z: INTEGRIN ALPHA M I DOMAIN MUTANT |
| 1na5: INTEGRIN ALPHA M I DOMAIN |
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External links
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| Alpha | |
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| Beta | |
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| Dimers | Cytoadhesin receptor: | |
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| Fibrinogen receptor: | |
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| Fibronectin receptor: | |
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| Leukocyte-adhesion receptor: | |
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| Very late antigen receptor: |
- Integrin alpha1beta1
- Integrin alpha2beta1
- Integrin alpha3beta1
- VLA-4
- Alpha-5 beta-1
- Integrin alpha6beta1
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| Vitronectin receptor: | |
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| see also cell surface receptor deficiencies |
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