Article ; Online: Current understanding on TREM-2 molecular biology and physiopathological functions.
International immunopharmacology
2024 Volume 134, Page(s) 112042
Abstract: Triggering receptor expressed on myeloid cells 2 (TREM-2), a glycosylated receptor belonging to the immunoglobin superfamily and especially expressed in the myeloid cell lineage, is frequently explained as a reminiscent receptor for both adaptive and ... ...
Abstract | Triggering receptor expressed on myeloid cells 2 (TREM-2), a glycosylated receptor belonging to the immunoglobin superfamily and especially expressed in the myeloid cell lineage, is frequently explained as a reminiscent receptor for both adaptive and innate immunity regulation. TREM-2 is also acknowledged to influence NK cell differentiation via the PI3K and PLCγ signaling pathways, as well as the partial activation or direct inhibition of T cells. Additionally, TREM-2 overexpression is substantially linked to cell-specific functions, such as enhanced phagocytosis, reduced toll-like receptor (TLR)-mediated inflammatory cytokine production, increased transcription of anti-inflammatory cytokines, and reshaped T cell function. Whereas TREM-2-deficient cells exhibit diminished phagocytic function and enhanced proinflammatory cytokines production, proceeding to inflammatory injuries and an immunosuppressive environment for disease progression. Despite the growing literature supporting TREM-2 |
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Language | English |
Publishing date | 2024-05-03 |
Publishing country | Netherlands |
Document type | Journal Article ; Review |
ZDB-ID | 2043785-7 |
ISSN | 1878-1705 ; 1567-5769 |
ISSN (online) | 1878-1705 |
ISSN | 1567-5769 |
DOI | 10.1016/j.intimp.2024.112042 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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