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 : 000589 ( Ncbi/Curation ); précédent : 000588; suivant : 000590Oligonucleotides 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
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pubmed:1833422Le document en format XML
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<placeName><region type="state">Maryland</region>
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<series><title level="j">The Journal of clinical investigation</title>
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<term>Base Sequence</term>
<term>Cells, Cultured</term>
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<term>Dose-Response Relationship, Drug</term>
<term>Fibroblasts (drug effects)</term>
<term>Humans</term>
<term>Interleukin-1 (antagonists & inhibitors)</term>
<term>Interleukin-1 (metabolism)</term>
<term>Liposomes (administration & dosage)</term>
<term>Mice</term>
<term>Molecular Sequence Data</term>
<term>Oligonucleotides, Antisense (pharmacology)</term>
<term>RNA, Messenger (genetics)</term>
<term>Receptors, Immunologic (analysis)</term>
<term>Receptors, Immunologic (genetics)</term>
<term>Receptors, Immunologic (physiology)</term>
<term>Receptors, Interleukin-1</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>ARN messager (génétique)</term>
<term>Animaux</term>
<term>Cellules cultivées</term>
<term>Dinoprostone (biosynthèse)</term>
<term>Données de séquences moléculaires</term>
<term>Fibroblastes ()</term>
<term>Humains</term>
<term>Interleukine-1 (antagonistes et inhibiteurs)</term>
<term>Interleukine-1 (métabolisme)</term>
<term>Liposomes (administration et posologie)</term>
<term>Oligonucléotides antisens (pharmacologie)</term>
<term>Relation dose-effet des médicaments</term>
<term>Récepteurs immunologiques (analyse)</term>
<term>Récepteurs immunologiques (génétique)</term>
<term>Récepteurs immunologiques (physiologie)</term>
<term>Récepteurs à l'interleukine-1</term>
<term>Souris</term>
<term>Séquence nucléotidique</term>
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<keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>Dinoprostone</term>
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<term>Récepteurs immunologiques</term>
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<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Oligonucléotides antisens</term>
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<term>Base Sequence</term>
<term>Cells, Cultured</term>
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<term>Mice</term>
<term>Molecular Sequence Data</term>
<term>Receptors, Interleukin-1</term>
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<term>Cellules cultivées</term>
<term>Données de séquences moléculaires</term>
<term>Fibroblastes</term>
<term>Humains</term>
<term>Relation dose-effet des médicaments</term>
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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>
</front>
</TEI>
</record>
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