Studies on Biosynthesis, Assembly and Expression of Human Major Transplantation Antigens

Biosynthesis and regulation of expression of transplantation antigens as detected by a monoclonal antibody to HLA‐A,B,C antigens (human leucocytic antigen) and a polyclonal antiserum to β2‐micro‐globulin have been investigated using radioactive amino acids and sugars to label human lymphoid cells. W...

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Publicado: 1980
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00142956_v103_n1_p197_ALGRANATI
http://hdl.handle.net/20.500.12110/paper_00142956_v103_n1_p197_ALGRANATI
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spelling paper:paper_00142956_v103_n1_p197_ALGRANATI2023-06-08T14:36:35Z Studies on Biosynthesis, Assembly and Expression of Human Major Transplantation Antigens histocompatibility antigen HLA antigen monoclonal antibody heredity human cell lymphatic system normal human beta 2-Microglobulin Beta-Globulins Cell Line Electrophoresis, Polyacrylamide Gel Epitopes Histocompatibility Antigens Human Lymphoid Tissue Macromolecular Systems Translation, Genetic Tunicamycin Biosynthesis and regulation of expression of transplantation antigens as detected by a monoclonal antibody to HLA‐A,B,C antigens (human leucocytic antigen) and a polyclonal antiserum to β2‐micro‐globulin have been investigated using radioactive amino acids and sugars to label human lymphoid cells. We found unbalanced synthesis of HLA heavy chains and β2‐microglobulin, the latter being in excess and secreted to the extracellular medium. In DAUDI cells, which are defective in β2‐microglobulin, no HLA‐A,B,C could be detected intracellularly even in the presence of added β2‐microglobulin. Treatment of BRI‐8 cells with tunicamycin, an antibiotic which inhibits glycosylation of polypeptides, almost had no effect on the levels of β2‐microglobulin, while it markedly decreased that of HLA heavy chains, both on the cell surface and intracellularly. Glycosylation of the HLA heavy chains appeared to be an essential requirement for the normal expression of HLA‐A,B,C antigens. The translation in vitro in a messenger‐dependent reticulocyte system with total polysomes obtained from BRI‐8 cells showed that β2‐microglobulin was synthesized as a precursor. This larger polypeptide was converted into mature β2‐microglobulin when protein synthesis was performed with microsomes instead of polysomes. Copyright © 1980, Wiley Blackwell. All rights reserved 1980 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00142956_v103_n1_p197_ALGRANATI http://hdl.handle.net/20.500.12110/paper_00142956_v103_n1_p197_ALGRANATI
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic histocompatibility antigen
HLA antigen
monoclonal antibody
heredity
human cell
lymphatic system
normal human
beta 2-Microglobulin
Beta-Globulins
Cell Line
Electrophoresis, Polyacrylamide Gel
Epitopes
Histocompatibility Antigens
Human
Lymphoid Tissue
Macromolecular Systems
Translation, Genetic
Tunicamycin
spellingShingle histocompatibility antigen
HLA antigen
monoclonal antibody
heredity
human cell
lymphatic system
normal human
beta 2-Microglobulin
Beta-Globulins
Cell Line
Electrophoresis, Polyacrylamide Gel
Epitopes
Histocompatibility Antigens
Human
Lymphoid Tissue
Macromolecular Systems
Translation, Genetic
Tunicamycin
Studies on Biosynthesis, Assembly and Expression of Human Major Transplantation Antigens
topic_facet histocompatibility antigen
HLA antigen
monoclonal antibody
heredity
human cell
lymphatic system
normal human
beta 2-Microglobulin
Beta-Globulins
Cell Line
Electrophoresis, Polyacrylamide Gel
Epitopes
Histocompatibility Antigens
Human
Lymphoid Tissue
Macromolecular Systems
Translation, Genetic
Tunicamycin
description Biosynthesis and regulation of expression of transplantation antigens as detected by a monoclonal antibody to HLA‐A,B,C antigens (human leucocytic antigen) and a polyclonal antiserum to β2‐micro‐globulin have been investigated using radioactive amino acids and sugars to label human lymphoid cells. We found unbalanced synthesis of HLA heavy chains and β2‐microglobulin, the latter being in excess and secreted to the extracellular medium. In DAUDI cells, which are defective in β2‐microglobulin, no HLA‐A,B,C could be detected intracellularly even in the presence of added β2‐microglobulin. Treatment of BRI‐8 cells with tunicamycin, an antibiotic which inhibits glycosylation of polypeptides, almost had no effect on the levels of β2‐microglobulin, while it markedly decreased that of HLA heavy chains, both on the cell surface and intracellularly. Glycosylation of the HLA heavy chains appeared to be an essential requirement for the normal expression of HLA‐A,B,C antigens. The translation in vitro in a messenger‐dependent reticulocyte system with total polysomes obtained from BRI‐8 cells showed that β2‐microglobulin was synthesized as a precursor. This larger polypeptide was converted into mature β2‐microglobulin when protein synthesis was performed with microsomes instead of polysomes. Copyright © 1980, Wiley Blackwell. All rights reserved
title Studies on Biosynthesis, Assembly and Expression of Human Major Transplantation Antigens
title_short Studies on Biosynthesis, Assembly and Expression of Human Major Transplantation Antigens
title_full Studies on Biosynthesis, Assembly and Expression of Human Major Transplantation Antigens
title_fullStr Studies on Biosynthesis, Assembly and Expression of Human Major Transplantation Antigens
title_full_unstemmed Studies on Biosynthesis, Assembly and Expression of Human Major Transplantation Antigens
title_sort studies on biosynthesis, assembly and expression of human major transplantation antigens
publishDate 1980
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00142956_v103_n1_p197_ALGRANATI
http://hdl.handle.net/20.500.12110/paper_00142956_v103_n1_p197_ALGRANATI
_version_ 1768543543817666560