Oligonucleotides antisense to the interleukin 1 receptor mRNA block the effects of interleukin 1 in cultured murine and human fibroblasts and in mice.
Identifieur interne : 002829 ( PubMed/Checkpoint ); précédent : 002828; suivant : 002830Oligonucleotides antisense to the interleukin 1 receptor mRNA block the effects of interleukin 1 in cultured murine and human fibroblasts and in mice.
Auteurs : R M Burch [États-Unis] ; L C MahanSource :
- The Journal of clinical investigation [ 0021-9738 ] ; 1991.
Descripteurs français
- KwdFr :
- ARN messager (génétique), Animaux, Cellules cultivées, Dinoprostone (biosynthèse), Données de séquences moléculaires, Fibroblastes (), Humains, Interleukine-1 (antagonistes et inhibiteurs), Interleukine-1 (métabolisme), Liposomes (administration et posologie), Oligonucléotides antisens (pharmacologie), Relation dose-effet des médicaments, Récepteurs immunologiques (analyse), Récepteurs immunologiques (génétique), Récepteurs immunologiques (physiologie), Récepteurs à l'interleukine-1, Souris, Séquence nucléotidique.
- MESH :
- administration et posologie : Liposomes.
- analyse : Récepteurs immunologiques.
- antagonistes et inhibiteurs : Interleukine-1.
- biosynthèse : Dinoprostone.
- génétique : ARN messager, Récepteurs immunologiques.
- métabolisme : Interleukine-1.
- pharmacologie : Oligonucléotides antisens.
- physiologie : Récepteurs immunologiques.
- Animaux, Cellules cultivées, Données de séquences moléculaires, Fibroblastes, Humains, Relation dose-effet des médicaments, Récepteurs à l'interleukine-1, Souris, Séquence nucléotidique.
English descriptors
- KwdEn :
- Animals, Base Sequence, Cells, Cultured, Dinoprostone (biosynthesis), Dose-Response Relationship, Drug, Fibroblasts (drug effects), Humans, Interleukin-1 (antagonists & inhibitors), Interleukin-1 (metabolism), Liposomes (administration & dosage), Mice, Molecular Sequence Data, Oligonucleotides, Antisense (pharmacology), RNA, Messenger (genetics), Receptors, Immunologic (analysis), Receptors, Immunologic (genetics), Receptors, Immunologic (physiology), Receptors, Interleukin-1.
- MESH :
- chemical , administration & dosage : Liposomes.
- chemical , analysis : Receptors, Immunologic.
- chemical , antagonists & inhibitors : Interleukin-1.
- chemical , biosynthesis : Dinoprostone.
- drug effects : Fibroblasts.
- chemical , genetics : RNA, Messenger, Receptors, Immunologic.
- chemical , metabolism : Interleukin-1.
- chemical , pharmacology : Oligonucleotides, Antisense.
- chemical , physiology : Receptors, Immunologic.
- Animals, Base Sequence, Cells, Cultured, Dose-Response Relationship, Drug, Humans, Mice, Molecular Sequence Data, Receptors, Interleukin-1.
Abstract
Phosphodiester and phosphorothioate oligodeoxynucleotides (18 mers) were constructed antisense to sequences of the recently cloned murine and human IL-1 receptors. Murine antisense oligonucleotides inhibited IL-1-stimulated PGE2 synthesis by murine fibroblasts in culture in a time (days) and concentration-dependent (3 microM-30 microM) fashion. Murine sense oligonucleotide and an oligonucleotide antisense to human IL-1 receptor were without effect. Moreover, murine antisense oligonucleotides did not affect tumor necrosis factor- or bradykinin-stimulated PGE2 synthesis by murine fibroblasts. Similarly, antisense oligonucleotides to the human, but not the murine, IL-1 receptor inhibited IL-1-stimulated PGE2 synthesis by cultured human fibroblasts. The attenuation of the cellular response to IL-1 caused by the antisense oligonucleotides correlated with a loss in cell surface receptors for IL-1, without any change in the number of bradykinin receptors on these cells. When antisense oligonucleotides were encapsulated in liposomes, they blocked completely the appearance of newly synthesized IL-1 receptors and IL-1-stimulated PGE2 synthesis. In mice, subcutaneous injection with an oligonucleotide antisense to the murine IL-1 receptor markedly inhibited the infiltration of neutrophils in response to subsequent injection of IL-1. These data suggest that antisense oligodeoxynucleotides may share a role in the design of antiinflammatory therapeutics.
DOI: 10.1172/JCI115421
PubMed: 1833422
Affiliations:
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pubmed:1833422Le document en format XML
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<front><div type="abstract" xml:lang="en">Phosphodiester and phosphorothioate oligodeoxynucleotides (18 mers) were constructed antisense to sequences of the recently cloned murine and human IL-1 receptors. Murine antisense oligonucleotides inhibited IL-1-stimulated PGE2 synthesis by murine fibroblasts in culture in a time (days) and concentration-dependent (3 microM-30 microM) fashion. Murine sense oligonucleotide and an oligonucleotide antisense to human IL-1 receptor were without effect. Moreover, murine antisense oligonucleotides did not affect tumor necrosis factor- or bradykinin-stimulated PGE2 synthesis by murine fibroblasts. Similarly, antisense oligonucleotides to the human, but not the murine, IL-1 receptor inhibited IL-1-stimulated PGE2 synthesis by cultured human fibroblasts. The attenuation of the cellular response to IL-1 caused by the antisense oligonucleotides correlated with a loss in cell surface receptors for IL-1, without any change in the number of bradykinin receptors on these cells. When antisense oligonucleotides were encapsulated in liposomes, they blocked completely the appearance of newly synthesized IL-1 receptors and IL-1-stimulated PGE2 synthesis. In mice, subcutaneous injection with an oligonucleotide antisense to the murine IL-1 receptor markedly inhibited the infiltration of neutrophils in response to subsequent injection of IL-1. These data suggest that antisense oligodeoxynucleotides may share a role in the design of antiinflammatory therapeutics.</div>
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<Abstract><AbstractText>Phosphodiester and phosphorothioate oligodeoxynucleotides (18 mers) were constructed antisense to sequences of the recently cloned murine and human IL-1 receptors. Murine antisense oligonucleotides inhibited IL-1-stimulated PGE2 synthesis by murine fibroblasts in culture in a time (days) and concentration-dependent (3 microM-30 microM) fashion. Murine sense oligonucleotide and an oligonucleotide antisense to human IL-1 receptor were without effect. Moreover, murine antisense oligonucleotides did not affect tumor necrosis factor- or bradykinin-stimulated PGE2 synthesis by murine fibroblasts. Similarly, antisense oligonucleotides to the human, but not the murine, IL-1 receptor inhibited IL-1-stimulated PGE2 synthesis by cultured human fibroblasts. The attenuation of the cellular response to IL-1 caused by the antisense oligonucleotides correlated with a loss in cell surface receptors for IL-1, without any change in the number of bradykinin receptors on these cells. When antisense oligonucleotides were encapsulated in liposomes, they blocked completely the appearance of newly synthesized IL-1 receptors and IL-1-stimulated PGE2 synthesis. In mice, subcutaneous injection with an oligonucleotide antisense to the murine IL-1 receptor markedly inhibited the infiltration of neutrophils in response to subsequent injection of IL-1. These data suggest that antisense oligodeoxynucleotides may share a role in the design of antiinflammatory therapeutics.</AbstractText>
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<Reference><Citation>Proc Natl Acad Sci U S A. 1989 Nov;86(22):8946-50</Citation>
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<Reference><Citation>Proc Natl Acad Sci U S A. 1989 Oct;86(20):8034-8</Citation>
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<Reference><Citation>Proc Natl Acad Sci U S A. 1989 Oct;86(20):8029-33</Citation>
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