Human Interaction Network Ontology

Last uploaded: June 27, 2014
Preferred Name

Interaction of DAP12 and TREM1
Synonyms
Definitions

TREM proteins (triggering receptors expressed on myeloid cells) are a family of cell surface receptors involved in innate immune responses. They are expressed in myeloid cells and have both positive and negative functions in regulating myeloid cell activation and differentiation. Humans have two members, TREM1 and TREM2. TREM1 is considered an amplifier of the immune response, while TREM2 is believed to be a negative regulator of inflammatory responses (Sharif & Knaap 2008). TREM proteins consist of a single extracellular V-type Ig-like domain, a transmembrane region and a short cytoplasmic tail lacking any signalling motifs (Kelker et al. 2004). Both receptors associate with DAP12 for signalling. <br>The ligand for TREM1 is unknown. TREM1 associates with DAP12 dimer. This interaction is mediated by aspartic acid and adjacent threonine residues in the DAP12 dimer that interface with lysine residues in the TREM1 transmembrane region. TREM1 engagement triggers the production of inflammatory chemokines and cytokines such as IL-8 and myeloperoxidase (MPO) in neutrophils and IL-8, MCP-1, and TNF in monocytes (Tessarz & Cerwenka 2008, Bouchon et al. 2000). Edited: Garapati, P V, 2012-05-25 Reviewed: Lanier, Lewis L, 2012-08-09 Authored: Garapati, P V, 2012-05-25

ID

http://purl.obolibrary.org/obo/HINO_0007782

comment

TREM proteins (triggering receptors expressed on myeloid cells) are a family of cell surface receptors involved in innate immune responses. They are expressed in myeloid cells and have both positive and negative functions in regulating myeloid cell activation and differentiation. Humans have two members, TREM1 and TREM2. TREM1 is considered an amplifier of the immune response, while TREM2 is believed to be a negative regulator of inflammatory responses (Sharif & Knaap 2008). TREM proteins consist of a single extracellular V-type Ig-like domain, a transmembrane region and a short cytoplasmic tail lacking any signalling motifs (Kelker et al. 2004). Both receptors associate with DAP12 for signalling.
The ligand for TREM1 is unknown. TREM1 associates with DAP12 dimer. This interaction is mediated by aspartic acid and adjacent threonine residues in the DAP12 dimer that interface with lysine residues in the TREM1 transmembrane region. TREM1 engagement triggers the production of inflammatory chemokines and cytokines such as IL-8 and myeloperoxidase (MPO) in neutrophils and IL-8, MCP-1, and TNF in monocytes (Tessarz & Cerwenka 2008, Bouchon et al. 2000).

Edited: Garapati, P V, 2012-05-25

Reviewed: Lanier, Lewis L, 2012-08-09

Authored: Garapati, P V, 2012-05-25

definition source

Pubmed10799849

Pubmed18926286

Reactome, http://www.reactome.org

Pubmed17110943

Pubmed15351648

Pubmed18192027

Pubmed12776204

Pubmed15884055

has input

http://purl.obolibrary.org/obo/UniProt_Q9NP99

http://purl.obolibrary.org/obo/HINO_0018207

has output

http://purl.obolibrary.org/obo/HINO_0002849

label

Interaction of DAP12 and TREM1

prefixIRI

HINO:0007782

prefLabel

Interaction of DAP12 and TREM1

seeAlso

Reactome Database ID Release 43210292

ReactomeREACT_147897

subClassOf

http://purl.obolibrary.org/obo/INO_0000040

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