id paper:paper_01615890_v26_n7_p601_Cremaschi
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spelling paper:paper_01615890_v26_n7_p601_Cremaschi2023-06-08T15:13:29Z Colchicine blocks β adrenoceptor and class I antigen-specific interactions alloantibody alloantigens colchicine cytoskeletal proteins β adrenoceptor alloantibody beta adrenergic receptor colchicine cyclic amp cytoskeleton protein hormone receptor immunoglobulin g major histocompatibility antigen class 1 animal cell animal experiment biological model cell culture cytochemistry heart immunization lymphocyte mouse nonhuman priority journal spleen cell Animal Binding, Competitive Colchicine Cyclic AMP Cytochalasin B H-2 Antigens Immunoglobulin G Isoantibodies Mice Mice, Inbred BALB C Mice, Inbred C3H Receptors, Adrenergic, beta Spleen Support, Non-U.S. Gov't Previously we have demonstrated a molecular relationship between H-2 class I antigens and β adrenoceptors from cardiac tissue. Here we show this type of interaction taking place with β adrenoceptors from splenic cells and their purified membranes and the participation of cytoskeletal proteins in the phenomenon. Alloimmune, as well as anti-class I but not anti-class II, antibodies were able to inhibit in a competitive manner the binding of (-)-[3 H]dihydroalprenolol to splenic lymphocytes and their purified membranes, and to increase cyclic AMP levels in intact cells as a consequence of β adrenoceptor activation. Furthermore, colchicine (a microtubule disrupting drug), but not cytochalasine B (a microfilament disrupting drug), was able to abrogate alloimmune antibody inhibition over the β radioligand binding to its receptor on both intact splenocytes and their membranes. Alloantibody actions were significantly diminished by peripheral protein solubilization in purified spleen cell membranes. These data pointed indirectly to the participation of a colchicine binding protein in class I antigen and hormone-receptor associations. © 1989. 1989 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01615890_v26_n7_p601_Cremaschi http://hdl.handle.net/20.500.12110/paper_01615890_v26_n7_p601_Cremaschi
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic alloantibody
alloantigens
colchicine
cytoskeletal proteins
β adrenoceptor
alloantibody
beta adrenergic receptor
colchicine
cyclic amp
cytoskeleton protein
hormone receptor
immunoglobulin g
major histocompatibility antigen class 1
animal cell
animal experiment
biological model
cell culture
cytochemistry
heart
immunization
lymphocyte
mouse
nonhuman
priority journal
spleen cell
Animal
Binding, Competitive
Colchicine
Cyclic AMP
Cytochalasin B
H-2 Antigens
Immunoglobulin G
Isoantibodies
Mice
Mice, Inbred BALB C
Mice, Inbred C3H
Receptors, Adrenergic, beta
Spleen
Support, Non-U.S. Gov't
spellingShingle alloantibody
alloantigens
colchicine
cytoskeletal proteins
β adrenoceptor
alloantibody
beta adrenergic receptor
colchicine
cyclic amp
cytoskeleton protein
hormone receptor
immunoglobulin g
major histocompatibility antigen class 1
animal cell
animal experiment
biological model
cell culture
cytochemistry
heart
immunization
lymphocyte
mouse
nonhuman
priority journal
spleen cell
Animal
Binding, Competitive
Colchicine
Cyclic AMP
Cytochalasin B
H-2 Antigens
Immunoglobulin G
Isoantibodies
Mice
Mice, Inbred BALB C
Mice, Inbred C3H
Receptors, Adrenergic, beta
Spleen
Support, Non-U.S. Gov't
Colchicine blocks β adrenoceptor and class I antigen-specific interactions
topic_facet alloantibody
alloantigens
colchicine
cytoskeletal proteins
β adrenoceptor
alloantibody
beta adrenergic receptor
colchicine
cyclic amp
cytoskeleton protein
hormone receptor
immunoglobulin g
major histocompatibility antigen class 1
animal cell
animal experiment
biological model
cell culture
cytochemistry
heart
immunization
lymphocyte
mouse
nonhuman
priority journal
spleen cell
Animal
Binding, Competitive
Colchicine
Cyclic AMP
Cytochalasin B
H-2 Antigens
Immunoglobulin G
Isoantibodies
Mice
Mice, Inbred BALB C
Mice, Inbred C3H
Receptors, Adrenergic, beta
Spleen
Support, Non-U.S. Gov't
description Previously we have demonstrated a molecular relationship between H-2 class I antigens and β adrenoceptors from cardiac tissue. Here we show this type of interaction taking place with β adrenoceptors from splenic cells and their purified membranes and the participation of cytoskeletal proteins in the phenomenon. Alloimmune, as well as anti-class I but not anti-class II, antibodies were able to inhibit in a competitive manner the binding of (-)-[3 H]dihydroalprenolol to splenic lymphocytes and their purified membranes, and to increase cyclic AMP levels in intact cells as a consequence of β adrenoceptor activation. Furthermore, colchicine (a microtubule disrupting drug), but not cytochalasine B (a microfilament disrupting drug), was able to abrogate alloimmune antibody inhibition over the β radioligand binding to its receptor on both intact splenocytes and their membranes. Alloantibody actions were significantly diminished by peripheral protein solubilization in purified spleen cell membranes. These data pointed indirectly to the participation of a colchicine binding protein in class I antigen and hormone-receptor associations. © 1989.
title Colchicine blocks β adrenoceptor and class I antigen-specific interactions
title_short Colchicine blocks β adrenoceptor and class I antigen-specific interactions
title_full Colchicine blocks β adrenoceptor and class I antigen-specific interactions
title_fullStr Colchicine blocks β adrenoceptor and class I antigen-specific interactions
title_full_unstemmed Colchicine blocks β adrenoceptor and class I antigen-specific interactions
title_sort colchicine blocks β adrenoceptor and class i antigen-specific interactions
publishDate 1989
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01615890_v26_n7_p601_Cremaschi
http://hdl.handle.net/20.500.12110/paper_01615890_v26_n7_p601_Cremaschi
_version_ 1768545323471339520