The DOI matches its Crossref record; 106 of the 106 references it cites were found in a registry or an index.
DAP10‐ and DAP12‐associated receptors in innate immunity
Open accessAbstract
Summary: The DAP10 and DAP12 signaling subunits are highly conserved in evolution and associate with a large family of receptors in hematopoietic cells, including dendritic cells, plasmacytoid dendritic cells, neutrophils, basophils, eosinophils, mast cells, monocytes, macrophages, natural killer cells, and some B and T cells. Some receptors are able to associate with either DAP10 or DAP12, which contribute unique intracellular signaling functions. Studies of humans and mice deficient in these signaling subunits have provided surprising insights into the physiological functions of DAP10 and DAP12, demonstrating that they can either activate or inhibit immune responses. DAP10‐ and DAP12‐associated receptors have been shown to recognize both host‐encoded ligands and ligands encoded by microbial pathogens, indicating that they play an important role in innate immune responses.
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Cites
Activation of NK Cells and T Cells by NKG2D, a Receptor for Stress-Inducible MICA
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Self-citationHLA-E binds to natural killer cell receptors CD94/NKG2A, B and C
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Self-citationUp on the tightrope: natural killer cell activation and inhibition
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Self-citationBouchon, A., Dietrich, J., & Colonna, M. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.10.4991 · Cited by 1,284
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Immunoreceptor DAP12 bearing a tyrosine-based activation motif is involved in activating NK cells
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Self-citationCostimulatory signals mediated by the ITAM motif cooperate with RANKL for bone homeostasis
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Natural Killer Cells: Development, Maturation, and Clinical Utilization
Abel, A. M., Yang, C., Thakar, M. S., & Malarkannan, S. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01869 · Cited by 1,150
Osteoimmunology: The conceptual framework unifying the immune and skeletal systems
Okamoto, K., Nakashima, T., Shinohara, M., Negishi-Koga, T., Komatsu, N., Terashima, A., Sawa, S., Nitta, T., & Takayanagi, H. (2017) · Physiological Reviews · doi:10.1152/physrev.00036.2016 · Cited by 534
TREM2 sustains microglial expansion during aging and response to demyelination
Poliani, P. L., Wang, Y., Fontana, E., Robinette, M. L., Yamanishi, Y., Gilfillan, S., & Colonna, M. (2015) · Journal of Clinical Investigation · doi:10.1172/jci77983 · Cited by 525
TREM2 drives microglia response to amyloid-β via SYK-dependent and -independent pathways
Wang, S., Sudan, R., Peng, V., Zhou, Y., Du, S., Yuede, C. M., Lei, T., Hou, J., Cai, Z., Cella, M., et al. (2022) · Cell · doi:10.1016/j.cell.2022.09.033 · Cited by 471
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Metadata
- Authors
- Lanier, L. L.
- Venue
- Immunological Reviews
- Publisher
- Wiley
- Published
- 2008-12-19
- Volume
- 227
- Issue
- 1
- Pages
- 150-160
- ISSN
- 0105-2896 (ISSN-L)
- 1600-065X
- OpenAlex
- W2090316299
- Cited by
- 323
- References
- 106
- FWCI
- 0.65
- Type
- journal article
- Language
- en
- Open access
- green
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