Alloimmune B-lymphocytes modify the myocardium contractility-inducing release of SRS-A

It has been previously demonstrated that murine alloimmune lymphoid cells were able to exert positive or negative inotropic effects on isolated mouse atria depending on the cellular type used. Here we show that BALB/c anti-C3H B-cells induced positive inotropic action on C3H mouse atria. Supernatant...

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Autores principales: Genaro, A.M., Borda, E.
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_01920561_v10_n5_p563_Genaro
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spelling todo:paper_01920561_v10_n5_p563_Genaro2023-10-03T15:09:05Z Alloimmune B-lymphocytes modify the myocardium contractility-inducing release of SRS-A Genaro, A.M. Borda, E. alloantigen slow reacting substance animal article B lymphocyte heart atrium heart contraction heart muscle immunology in vitro study mouse mouse strain Animal B-Lymphocytes Heart Atrium In Vitro Isoantigens Mice Mice, Inbred BALB C Mice, Inbred C3H Myocardial Contraction Myocardium SRS-A Support, Non-U.S. Gov't It has been previously demonstrated that murine alloimmune lymphoid cells were able to exert positive or negative inotropic effects on isolated mouse atria depending on the cellular type used. Here we show that BALB/c anti-C3H B-cells induced positive inotropic action on C3H mouse atria. Supernatants of alloimmunized B-cells co-cultivated with C3H myocardium exerted the same biological effect as alloimmune B-cells, indicating that a soluble factor is involved. Inhibitors of lipoxygenase(s) of arachidonic acid metabolism and a SRS-A blocker inhibited the positive effect of immune cells or its supernatants. The effect was prevented when we inhibited the atria lipoxygenase activity. On the other hand, when the inhibitors were applied to effector cells the response was not modified. In addition, supernatants of B-cells cultured with alloextracts were inactive. Supernatants from alloimmune B-cells plus myocardium release higher amounts of LTC4 than those from normal B-cells. It is proposed that SRS-A synthesis is induced in the atria by direct contact with alloimmune B-cells upon recognition of alloantigens expressed by atria cells; which in turn, triggers the positive inotropic effect. © 1988. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_01920561_v10_n5_p563_Genaro
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic alloantigen
slow reacting substance
animal
article
B lymphocyte
heart atrium
heart contraction
heart muscle
immunology
in vitro study
mouse
mouse strain
Animal
B-Lymphocytes
Heart Atrium
In Vitro
Isoantigens
Mice
Mice, Inbred BALB C
Mice, Inbred C3H
Myocardial Contraction
Myocardium
SRS-A
Support, Non-U.S. Gov't
spellingShingle alloantigen
slow reacting substance
animal
article
B lymphocyte
heart atrium
heart contraction
heart muscle
immunology
in vitro study
mouse
mouse strain
Animal
B-Lymphocytes
Heart Atrium
In Vitro
Isoantigens
Mice
Mice, Inbred BALB C
Mice, Inbred C3H
Myocardial Contraction
Myocardium
SRS-A
Support, Non-U.S. Gov't
Genaro, A.M.
Borda, E.
Alloimmune B-lymphocytes modify the myocardium contractility-inducing release of SRS-A
topic_facet alloantigen
slow reacting substance
animal
article
B lymphocyte
heart atrium
heart contraction
heart muscle
immunology
in vitro study
mouse
mouse strain
Animal
B-Lymphocytes
Heart Atrium
In Vitro
Isoantigens
Mice
Mice, Inbred BALB C
Mice, Inbred C3H
Myocardial Contraction
Myocardium
SRS-A
Support, Non-U.S. Gov't
description It has been previously demonstrated that murine alloimmune lymphoid cells were able to exert positive or negative inotropic effects on isolated mouse atria depending on the cellular type used. Here we show that BALB/c anti-C3H B-cells induced positive inotropic action on C3H mouse atria. Supernatants of alloimmunized B-cells co-cultivated with C3H myocardium exerted the same biological effect as alloimmune B-cells, indicating that a soluble factor is involved. Inhibitors of lipoxygenase(s) of arachidonic acid metabolism and a SRS-A blocker inhibited the positive effect of immune cells or its supernatants. The effect was prevented when we inhibited the atria lipoxygenase activity. On the other hand, when the inhibitors were applied to effector cells the response was not modified. In addition, supernatants of B-cells cultured with alloextracts were inactive. Supernatants from alloimmune B-cells plus myocardium release higher amounts of LTC4 than those from normal B-cells. It is proposed that SRS-A synthesis is induced in the atria by direct contact with alloimmune B-cells upon recognition of alloantigens expressed by atria cells; which in turn, triggers the positive inotropic effect. © 1988.
format JOUR
author Genaro, A.M.
Borda, E.
author_facet Genaro, A.M.
Borda, E.
author_sort Genaro, A.M.
title Alloimmune B-lymphocytes modify the myocardium contractility-inducing release of SRS-A
title_short Alloimmune B-lymphocytes modify the myocardium contractility-inducing release of SRS-A
title_full Alloimmune B-lymphocytes modify the myocardium contractility-inducing release of SRS-A
title_fullStr Alloimmune B-lymphocytes modify the myocardium contractility-inducing release of SRS-A
title_full_unstemmed Alloimmune B-lymphocytes modify the myocardium contractility-inducing release of SRS-A
title_sort alloimmune b-lymphocytes modify the myocardium contractility-inducing release of srs-a
url http://hdl.handle.net/20.500.12110/paper_01920561_v10_n5_p563_Genaro
work_keys_str_mv AT genaroam alloimmuneblymphocytesmodifythemyocardiumcontractilityinducingreleaseofsrsa
AT bordae alloimmuneblymphocytesmodifythemyocardiumcontractilityinducingreleaseofsrsa
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