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PMID: 3130455 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Differential induction of H-2K versus H-2D class I major histocompatibility antigens by recombinant gamma interferon. Lack of Kk augmentation in a leukemia virus-induced tumor is due to a cis-dominant effect.

The Journal of experimental medicine ·Vol. 167 ·No. 5 ·1988-05-01 ·Pages 1616-24

Green WR, Rich RF, Beadling C

Abstract

T-T tumor hybrids were constructed between the AKR SL3 thymoma and an H-2-distinguishable thymoma cell line. Hybrids were stimulated with IFN-gamma to determine whether the differential augmentation of H-2D vs. H-2K class I antigen expression by AKR SL3 in response to IFN-gamma was due to effects cis or trans to the noninducible Kk gene. For each of a large number of hybrids tested, the expression of H-2Db, Kb, and Dk, but not Kk, was substantially enhanced by murine rIFN-gamma. These results suggested that the lack of induction of the Kk gene was due to an alteration cis to Kk rather than to the presence or absence of K region-specific, trans-acting negative or positive factors, respectively.

MeSH Terms
AKR murine leukemia virus Animals Antigens, Neoplasm/biosynthesis,genetics Gene Expression Regulation/drug effects H-2 Antigens/biosynthesis,genetics Histocompatibility Antigen H-2D Interferon-gamma/pharmacology Leukemia, Experimental/genetics,immunology Mice Mice, Inbred C57BL Recombinant Proteins/pharmacology Tumor Cells, Cultured/immunology
Chemicals
Antigens, Neoplasm H-2 Antigens H-2K(K) antigen Histocompatibility Antigen H-2D Recombinant Proteins Interferon-gamma
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Green W R
Department of Microbiology, Dartmouth Medical School, Hanover, New Hampshire 03756.
Rich R F
Beadling C
References (15)
15 references, click to expand
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1988-05-01
Pages
1616-24
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2188948
Subset
IM
Grants
NCI NIH HHS · CA-23108 · United States
NCI NIH HHS · CA-36860 · United States
NCI NIH HHS · CA-43475 · United States
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