The T cell antigen receptor complex expressed on normal peripheral blood CD4-, CD8- T lymphocytes. A CD3-associated disulfide-linked gamma chain heterodimer
The T cell antigen receptor complex expressed on normal peripheral blood CD4-, CD8- T lymphocytes. A CD3-associated disulfide-linked gamma chain heterodimer
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T细胞抗原受体复合物表达于正常外周血CD4-、CD8-T淋巴细胞上。
DOI:
--
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发表时间:
1987
影响因子:
15.3
通讯作者:
A. Weiss
中科院分区:
文献类型:
--
作者:
L. Lanier;N. Federspiel;J. Ruitenberg;J. Phillips;J. Allison;D. Littman;A. Weiss
IL-2-dependent cell lines were established from normal peripheral blood T lymphocytes that express neither CD4 nor CD8 differentiation antigens. CD3+,4-,8- cell lines from 15 different donors failed to react with WT31, an mAb directed against the T cell antigen receptor alpha/beta heterodimer. Anti-Leu-4 mAb was used to isolate the CD3/T cell antigen receptor complex from 125I-labeled CD3+,4-,8- (WT31-) T cells. Using detergent conditions that preserved the CD3/T cell antigen receptor complex, an approximately 90 kD disulfide-linked heterodimer, composed of approximately 45- and approximately 40- (or approximately 37-) kD subunits, was coimmunoprecipitated with the invariant 20-29-kD CD3 complex. Analysis of these components by nonequilibrium pH gradient electrophoresis indicated that the approximately 40-kD and approximately 37-kD subunits were similar, and quite distinct from the more basic approximately 45-kD subunit. None of these three subunits reacted with an antibody directed against a beta chain framework epitope. Heteroantiserum against a T cell receptor gamma chain peptide specifically reacted with both the approximately 37- and approximately 40-kD CD3-associated proteins, but not with the approximately 45-kD subunit. CD3+,4-,8- cells failed to transcribe substantial amounts of functional 1.3-kb beta or 1.6-kb alpha mRNA, but produced abundant 1.6- kb gamma mRNA. Southern blot analysis revealed that these CD3+,4-,8- cell lines rearranged both gamma and beta genes, and indicated that the populations were polyclonal. The expression of a CD3-associated disulfide-linked heterodimer on CD3+,4-,8- T cell lines established from normal, adult peripheral blood contrasts with prior reports describing a CD3-associated non-disulfide-linked heterodimer on CD3+/WT31- cell lines established from thymus and peripheral blood obtained from patients with immunodeficiency diseases. We propose that this discrepancy may be explained by preferential usage of the two C gamma genes in T lymphocytes.
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DOI:
10.1073/pnas.82.10.3460
发表时间:
1985
影响因子:
11.1
作者:
Flug,F;Pelicci,PG;Bonetti,F;Knowles2nd,DM;Dalla-Favera,R
通讯作者:
Dalla-Favera,R
影响因子:
4.4
作者:
James P. Allison;Bradley W. McIntyre;D. Bloch
通讯作者:
James P. Allison;Bradley W. McIntyre;D. Bloch
DOI:
--
发表时间:
1985
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Spits,H;Borst,J;Tax,W;Capel,PJ;Terhorst,C;deVries,JE
通讯作者:
deVries,JE
DOI:
10.1126/science.3079918
发表时间:
1986
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Quertermous,T;Murre,C;Dialynas,D;Duby,AD;Strominger,JL;Waldman,TA;Seidman,JG
通讯作者:
Seidman,JG
DOI:
--
发表时间:
1984
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
Oettgen,HC;Kappler,J;Tax,WJ;Terhorst,C
通讯作者:
Terhorst,C