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PMID: 3317416 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Defective HLA class II expression in a regulatory mutant is partially complemented by activated ras oncogenes.

Hume CR, Accolla RS, Lee JS

Abstract

The human B-cell line RJ2.2.5, derived by mutagenesis from a Burkitt lymphoma cell line and selected for loss of HLA class II antigen expression, was infected with recombinant retroviruses containing either the Harvey murine sarcoma virus oncogene v-Ha-ras or the human neuroblastoma homolog NRAS. Both activated ras genes partially complemented the regulatory defect in RJ2.2.5 and specifically increased the expression of the DR and DQ subsets of HLA class II genes. Blot-hybridization analysis and RNase mapping indicated that HLA-DQ alpha-chain mRNA in the infected cell lines was increased to a level at least 50% that of the parent B-cell line, Raji. The levels of HLA-DR and -DQ beta-chain RNA also were increased but to a lesser extent. In contrast, we detected no effect of ras on the quantities of other class II, class I, or invariant-chain mRNAs. Fluorescence-activated cell sorter analysis with antibodies recognizing HLA-DR, -DQ, and class I antigens supported these observations. Enhancement of HLA class II gene expression by ras genes may have important implications for regulation of the immune system in response to transformation.

MeSH Terms
Antigens, Surface/genetics Cell Line Flow Cytometry Gene Expression Regulation Genes, ras HLA-D Antigens/genetics Humans Oncogene Proteins, Viral/physiology RNA, Messenger/genetics Transcription, Genetic
Chemicals
Antigens, Surface HLA-D Antigens Oncogene Proteins, Viral RNA, Messenger
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Hume C R
Immunology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10021.
Accolla R S
Lee J S
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1987-12-00
Pages
8603-7
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC299593
Subset
IM
Grants
NCI NIH HHS · 2P01 CA20194-10 · United States
NCI NIH HHS · CA-08748 · United States
NCRR NIH HHS · RR-05534 · United States
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