Cellular expression or binding of desLys58-beta2 microglobulin is not dependent on the presence of the tri-molecular MHC class I complex.

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Cellular expression or binding of desLys58-beta2 microglobulin is not dependent on the presence of the tri-molecular MHC class I complex. / Wang, M; Corlin, D B; Heegaard, N H H; Claesson, M H; Nissen, Mogens Holst.

In: Scandinavian Journal of Immunology, Vol. 67, No. 2, 2008, p. 105-12.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Wang, M, Corlin, DB, Heegaard, NHH, Claesson, MH & Nissen, MH 2008, 'Cellular expression or binding of desLys58-beta2 microglobulin is not dependent on the presence of the tri-molecular MHC class I complex.', Scandinavian Journal of Immunology, vol. 67, no. 2, pp. 105-12. https://doi.org/10.1111/j.1365-3083.2007.02044.x

APA

Wang, M., Corlin, D. B., Heegaard, N. H. H., Claesson, M. H., & Nissen, M. H. (2008). Cellular expression or binding of desLys58-beta2 microglobulin is not dependent on the presence of the tri-molecular MHC class I complex. Scandinavian Journal of Immunology, 67(2), 105-12. https://doi.org/10.1111/j.1365-3083.2007.02044.x

Vancouver

Wang M, Corlin DB, Heegaard NHH, Claesson MH, Nissen MH. Cellular expression or binding of desLys58-beta2 microglobulin is not dependent on the presence of the tri-molecular MHC class I complex. Scandinavian Journal of Immunology. 2008;67(2):105-12. https://doi.org/10.1111/j.1365-3083.2007.02044.x

Author

Wang, M ; Corlin, D B ; Heegaard, N H H ; Claesson, M H ; Nissen, Mogens Holst. / Cellular expression or binding of desLys58-beta2 microglobulin is not dependent on the presence of the tri-molecular MHC class I complex. In: Scandinavian Journal of Immunology. 2008 ; Vol. 67, No. 2. pp. 105-12.

Bibtex

@article{5b564ce0ba2d11ddae57000ea68e967b,
title = "Cellular expression or binding of desLys58-beta2 microglobulin is not dependent on the presence of the tri-molecular MHC class I complex.",
abstract = "The monoclonal antibody 332-01 is a newly developed antibody which specifically recognizes human desLys58-beta2 microglobulin (dbeta2m). In the present study, we characterized the binding of 332-01 to peripheral blood mononuclear cells (PBMC), a number of human leukaemic and monocytic cell lines, and beta2m gene-deleted murine lymphocytes. dbeta2m was found to be expressed on non-activated and activated monocytes. When cells were pre-exposed to dbeta2m, 332-01 also bound to non-activated T lymphocytes. dbeta2m was expressed on the monocytic cell lines U937 and TIB-202, and binding was significantly increased when cells were pre-incubated with dbeta2m and when TIB-202 cells were exposed to lipopolysaccharide. dbeta2m was also expressed on T leukaemic Jurkat cells as well as on low HLA-expressing erythroleukaemic K562 cells. beta2m gene-deleted murine splenocytes only bound 332-01 after pre-exposure to dbeta2m. Binding of 332-01 antibody could not be displaced by addition of high concentrations of native beta2m. In conclusion, our data indicate that dbeta2m - in contrast to native beta2m - binds to a hitherto unknown cell surface receptor independent of classical MHC class I molecules. As beta2m has previously been shown to display biological activities such as the induction of both growth promotion and apoptosis, C1 complement activity, shown to mediate cleavage of beta2m, could be involved in these processes.",
author = "M Wang and Corlin, {D B} and Heegaard, {N H H} and Claesson, {M H} and Nissen, {Mogens Holst}",
note = "Keywords: Animals; Antibodies, Monoclonal; Antibody Specificity; Female; Flow Cytometry; Histocompatibility Antigens Class I; Humans; Immunity, Cellular; Jurkat Cells; K562 Cells; Leukemia, T-Cell; Mice; Mice, Inbred C57BL; Mice, Knockout; Monocytes; Specific Pathogen-Free Organisms; T-Lymphocytes; U937 Cells; beta 2-Microglobulin",
year = "2008",
doi = "10.1111/j.1365-3083.2007.02044.x",
language = "English",
volume = "67",
pages = "105--12",
journal = "Scandinavian Journal of Immunology, Supplement",
issn = "0301-6323",
publisher = "Wiley-Blackwell",
number = "2",

}

RIS

TY - JOUR

T1 - Cellular expression or binding of desLys58-beta2 microglobulin is not dependent on the presence of the tri-molecular MHC class I complex.

AU - Wang, M

AU - Corlin, D B

AU - Heegaard, N H H

AU - Claesson, M H

AU - Nissen, Mogens Holst

N1 - Keywords: Animals; Antibodies, Monoclonal; Antibody Specificity; Female; Flow Cytometry; Histocompatibility Antigens Class I; Humans; Immunity, Cellular; Jurkat Cells; K562 Cells; Leukemia, T-Cell; Mice; Mice, Inbred C57BL; Mice, Knockout; Monocytes; Specific Pathogen-Free Organisms; T-Lymphocytes; U937 Cells; beta 2-Microglobulin

PY - 2008

Y1 - 2008

N2 - The monoclonal antibody 332-01 is a newly developed antibody which specifically recognizes human desLys58-beta2 microglobulin (dbeta2m). In the present study, we characterized the binding of 332-01 to peripheral blood mononuclear cells (PBMC), a number of human leukaemic and monocytic cell lines, and beta2m gene-deleted murine lymphocytes. dbeta2m was found to be expressed on non-activated and activated monocytes. When cells were pre-exposed to dbeta2m, 332-01 also bound to non-activated T lymphocytes. dbeta2m was expressed on the monocytic cell lines U937 and TIB-202, and binding was significantly increased when cells were pre-incubated with dbeta2m and when TIB-202 cells were exposed to lipopolysaccharide. dbeta2m was also expressed on T leukaemic Jurkat cells as well as on low HLA-expressing erythroleukaemic K562 cells. beta2m gene-deleted murine splenocytes only bound 332-01 after pre-exposure to dbeta2m. Binding of 332-01 antibody could not be displaced by addition of high concentrations of native beta2m. In conclusion, our data indicate that dbeta2m - in contrast to native beta2m - binds to a hitherto unknown cell surface receptor independent of classical MHC class I molecules. As beta2m has previously been shown to display biological activities such as the induction of both growth promotion and apoptosis, C1 complement activity, shown to mediate cleavage of beta2m, could be involved in these processes.

AB - The monoclonal antibody 332-01 is a newly developed antibody which specifically recognizes human desLys58-beta2 microglobulin (dbeta2m). In the present study, we characterized the binding of 332-01 to peripheral blood mononuclear cells (PBMC), a number of human leukaemic and monocytic cell lines, and beta2m gene-deleted murine lymphocytes. dbeta2m was found to be expressed on non-activated and activated monocytes. When cells were pre-exposed to dbeta2m, 332-01 also bound to non-activated T lymphocytes. dbeta2m was expressed on the monocytic cell lines U937 and TIB-202, and binding was significantly increased when cells were pre-incubated with dbeta2m and when TIB-202 cells were exposed to lipopolysaccharide. dbeta2m was also expressed on T leukaemic Jurkat cells as well as on low HLA-expressing erythroleukaemic K562 cells. beta2m gene-deleted murine splenocytes only bound 332-01 after pre-exposure to dbeta2m. Binding of 332-01 antibody could not be displaced by addition of high concentrations of native beta2m. In conclusion, our data indicate that dbeta2m - in contrast to native beta2m - binds to a hitherto unknown cell surface receptor independent of classical MHC class I molecules. As beta2m has previously been shown to display biological activities such as the induction of both growth promotion and apoptosis, C1 complement activity, shown to mediate cleavage of beta2m, could be involved in these processes.

U2 - 10.1111/j.1365-3083.2007.02044.x

DO - 10.1111/j.1365-3083.2007.02044.x

M3 - Journal article

C2 - 18069937

VL - 67

SP - 105

EP - 112

JO - Scandinavian Journal of Immunology, Supplement

JF - Scandinavian Journal of Immunology, Supplement

SN - 0301-6323

IS - 2

ER -

ID: 8746021