The KIR and CD94/NKG2 families of molecules in the rhesus monkey - PubMed (original) (raw)
Review
The KIR and CD94/NKG2 families of molecules in the rhesus monkey
M L LaBonte et al. Immunol Rev. 2001 Oct.
Abstract
Natural killer (NK) cells and a subset of T cells express families of receptors that are capable of detecting major histocompatibility complex (MHC) class I expression on the surface of cells. Molecules of the killer cell immunoglobulin-like receptor (KIR) family bind directly to MHC class I, while those of the CD94/NKG2 family recognize MHC class I signal sequences bound to HLA-E. Both the KIR and CD94/NKG2 families are composed of activating and inhibitory molecules that serve to regulate the function of NK cells as a result of their MHC class I recognition. Here we review the recently described KIR and CD94/NKG2 family members in the rhesus monkey.
Similar articles
- Structure and function of major histocompatibility complex (MHC) class I specific receptors expressed on human natural killer (NK) cells.
Borrego F, Kabat J, Kim DK, Lieto L, Maasho K, Peña J, Solana R, Coligan JE. Borrego F, et al. Mol Immunol. 2002 Feb;38(9):637-60. doi: 10.1016/s0161-5890(01)00107-9. Mol Immunol. 2002. PMID: 11858820 Review. - The activating form of CD94 receptor complex: CD94 covalently associates with the Kp39 protein that represents the product of the NKG2-C gene.
Cantoni C, Biassoni R, Pende D, Sivori S, Accame L, Pareti L, Semenzato G, Moretta L, Moretta A, Bottino C. Cantoni C, et al. Eur J Immunol. 1998 Jan;28(1):327-38. doi: 10.1002/(SICI)1521-4141(199801)28:01<327::AID-IMMU327>3.0.CO;2-O. Eur J Immunol. 1998. PMID: 9485212 - Natural killer cell recognition of HLA class I molecules.
Brooks AG, Boyington JC, Sun PD. Brooks AG, et al. Rev Immunogenet. 2000;2(3):433-48. Rev Immunogenet. 2000. PMID: 11256749 Review. - Expression of Ly49E and CD94/NKG2 on fetal and adult NK cells.
Van Beneden K, Stevenaert F, De Creus A, Debacker V, De Boever J, Plum J, Leclercq G. Van Beneden K, et al. J Immunol. 2001 Apr 1;166(7):4302-11. doi: 10.4049/jimmunol.166.7.4302. J Immunol. 2001. PMID: 11254682 - Kinetics and peptide dependency of the binding of the inhibitory NK receptor CD94/NKG2-A and the activating receptor CD94/NKG2-C to HLA-E.
Valés-Gómez M, Reyburn HT, Erskine RA, López-Botet M, Strominger JL. Valés-Gómez M, et al. EMBO J. 1999 Aug 2;18(15):4250-60. doi: 10.1093/emboj/18.15.4250. EMBO J. 1999. PMID: 10428963 Free PMC article.
Cited by
- Genetic engineering of pigs for xenotransplantation to overcome immune rejection and physiological incompatibilities: The first clinical steps.
Lei T, Chen L, Wang K, Du S, Gonelle-Gispert C, Wang Y, Buhler LH. Lei T, et al. Front Immunol. 2022 Dec 6;13:1031185. doi: 10.3389/fimmu.2022.1031185. eCollection 2022. Front Immunol. 2022. PMID: 36561750 Free PMC article. Review. - Monkeying Around: Using Non-human Primate Models to Study NK Cell Biology in HIV Infections.
Manickam C, Shah SV, Nohara J, Ferrari G, Reeves RK. Manickam C, et al. Front Immunol. 2019 May 22;10:1124. doi: 10.3389/fimmu.2019.01124. eCollection 2019. Front Immunol. 2019. PMID: 31191520 Free PMC article. Review. - The Role of NK Cells in Pig-to-Human Xenotransplantation.
Puga Yung G, Schneider MKJ, Seebach JD. Puga Yung G, et al. J Immunol Res. 2017;2017:4627384. doi: 10.1155/2017/4627384. Epub 2017 Dec 19. J Immunol Res. 2017. PMID: 29410970 Free PMC article. Review. - Diversification of both KIR and NKG2 natural killer cell receptor genes in macaques - implications for highly complex MHC-dependent regulation of natural killer cells.
Walter L, Petersen B. Walter L, et al. Immunology. 2017 Feb;150(2):139-145. doi: 10.1111/imm.12666. Epub 2016 Oct 5. Immunology. 2017. PMID: 27565739 Free PMC article. Review. - The evolution of natural killer cell receptors.
Carrillo-Bustamante P, Keşmir C, de Boer RJ. Carrillo-Bustamante P, et al. Immunogenetics. 2016 Jan;68(1):3-18. doi: 10.1007/s00251-015-0869-7. Epub 2015 Sep 21. Immunogenetics. 2016. PMID: 26392015 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials