Cargando…

Modulation of Pro-Inflammatory IL-6 Trans-Signaling Axis by Splice Switching Oligonucleotides as a Therapeutic Modality in Inflammation

Interleukin-6 (IL-6) is a pleiotropic cytokine that plays a crucial role in maintaining normal homeostatic processes under the pathogenesis of various inflammatory and autoimmune diseases. This context-dependent effect from a cytokine is due to two distinctive forms of signaling: cis-signaling and t...

Descripción completa

Detalles Bibliográficos
Autores principales: Gupta, Dhanu, Orehek, Sara, Turunen, Janne, O’Donovan, Liz, Gait, Michael J., El-Andaloussi, Samir, Wood, Matthew J. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10526877/
https://www.ncbi.nlm.nih.gov/pubmed/37759507
http://dx.doi.org/10.3390/cells12182285
_version_ 1785111088673587200
author Gupta, Dhanu
Orehek, Sara
Turunen, Janne
O’Donovan, Liz
Gait, Michael J.
El-Andaloussi, Samir
Wood, Matthew J. A.
author_facet Gupta, Dhanu
Orehek, Sara
Turunen, Janne
O’Donovan, Liz
Gait, Michael J.
El-Andaloussi, Samir
Wood, Matthew J. A.
author_sort Gupta, Dhanu
collection PubMed
description Interleukin-6 (IL-6) is a pleiotropic cytokine that plays a crucial role in maintaining normal homeostatic processes under the pathogenesis of various inflammatory and autoimmune diseases. This context-dependent effect from a cytokine is due to two distinctive forms of signaling: cis-signaling and trans-signaling. IL-6 cis-signaling involves binding IL-6 to the membrane-bound IL-6 receptor and Glycoprotein 130 (GP130) signal-transducing subunit. By contrast, in IL-6 trans-signaling, complexes of IL-6 and the soluble form of the IL-6 receptor (sIL-6R) signal via membrane-bound GP130. Various strategies have been employed in the past decade to target the pro-inflammatory effect of IL-6 in numerous inflammatory disorders. However, their development has been hindered since these approaches generally target global IL-6 signaling, also affecting the anti-inflammatory effects of IL-6 signaling too. Therefore, novel strategies explicitly targeting the pro-inflammatory IL-6 trans-signaling without affecting the IL-6 cis-signaling are required and carry immense therapeutic potential. Here, we have developed a novel approach to specifically decoy IL-6-mediated trans-signaling by modulating alternative splicing in GP130, an IL-6 signal transducer, by employing splice switching oligonucleotides (SSO), to induce the expression of truncated soluble isoforms of the protein GP130. This isoform is devoid of signaling domains but allows for specifically sequestering the IL-6/sIL-6R receptor complex with high affinity in serum and thereby suppressing inflammation. Using the state-of-the-art Pip6a cell-penetrating peptide conjugated to PMO-based SSO targeting GP130 for efficient in vivo delivery, reduced disease phenotypes in two different inflammatory mouse models of systemic and intestinal inflammation were observed. Overall, this novel gene therapy platform holds great potential as a refined therapeutic intervention for chronic inflammatory diseases.
format Online
Article
Text
id pubmed-10526877
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-105268772023-09-28 Modulation of Pro-Inflammatory IL-6 Trans-Signaling Axis by Splice Switching Oligonucleotides as a Therapeutic Modality in Inflammation Gupta, Dhanu Orehek, Sara Turunen, Janne O’Donovan, Liz Gait, Michael J. El-Andaloussi, Samir Wood, Matthew J. A. Cells Article Interleukin-6 (IL-6) is a pleiotropic cytokine that plays a crucial role in maintaining normal homeostatic processes under the pathogenesis of various inflammatory and autoimmune diseases. This context-dependent effect from a cytokine is due to two distinctive forms of signaling: cis-signaling and trans-signaling. IL-6 cis-signaling involves binding IL-6 to the membrane-bound IL-6 receptor and Glycoprotein 130 (GP130) signal-transducing subunit. By contrast, in IL-6 trans-signaling, complexes of IL-6 and the soluble form of the IL-6 receptor (sIL-6R) signal via membrane-bound GP130. Various strategies have been employed in the past decade to target the pro-inflammatory effect of IL-6 in numerous inflammatory disorders. However, their development has been hindered since these approaches generally target global IL-6 signaling, also affecting the anti-inflammatory effects of IL-6 signaling too. Therefore, novel strategies explicitly targeting the pro-inflammatory IL-6 trans-signaling without affecting the IL-6 cis-signaling are required and carry immense therapeutic potential. Here, we have developed a novel approach to specifically decoy IL-6-mediated trans-signaling by modulating alternative splicing in GP130, an IL-6 signal transducer, by employing splice switching oligonucleotides (SSO), to induce the expression of truncated soluble isoforms of the protein GP130. This isoform is devoid of signaling domains but allows for specifically sequestering the IL-6/sIL-6R receptor complex with high affinity in serum and thereby suppressing inflammation. Using the state-of-the-art Pip6a cell-penetrating peptide conjugated to PMO-based SSO targeting GP130 for efficient in vivo delivery, reduced disease phenotypes in two different inflammatory mouse models of systemic and intestinal inflammation were observed. Overall, this novel gene therapy platform holds great potential as a refined therapeutic intervention for chronic inflammatory diseases. MDPI 2023-09-15 /pmc/articles/PMC10526877/ /pubmed/37759507 http://dx.doi.org/10.3390/cells12182285 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gupta, Dhanu
Orehek, Sara
Turunen, Janne
O’Donovan, Liz
Gait, Michael J.
El-Andaloussi, Samir
Wood, Matthew J. A.
Modulation of Pro-Inflammatory IL-6 Trans-Signaling Axis by Splice Switching Oligonucleotides as a Therapeutic Modality in Inflammation
title Modulation of Pro-Inflammatory IL-6 Trans-Signaling Axis by Splice Switching Oligonucleotides as a Therapeutic Modality in Inflammation
title_full Modulation of Pro-Inflammatory IL-6 Trans-Signaling Axis by Splice Switching Oligonucleotides as a Therapeutic Modality in Inflammation
title_fullStr Modulation of Pro-Inflammatory IL-6 Trans-Signaling Axis by Splice Switching Oligonucleotides as a Therapeutic Modality in Inflammation
title_full_unstemmed Modulation of Pro-Inflammatory IL-6 Trans-Signaling Axis by Splice Switching Oligonucleotides as a Therapeutic Modality in Inflammation
title_short Modulation of Pro-Inflammatory IL-6 Trans-Signaling Axis by Splice Switching Oligonucleotides as a Therapeutic Modality in Inflammation
title_sort modulation of pro-inflammatory il-6 trans-signaling axis by splice switching oligonucleotides as a therapeutic modality in inflammation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10526877/
https://www.ncbi.nlm.nih.gov/pubmed/37759507
http://dx.doi.org/10.3390/cells12182285
work_keys_str_mv AT guptadhanu modulationofproinflammatoryil6transsignalingaxisbyspliceswitchingoligonucleotidesasatherapeuticmodalityininflammation
AT oreheksara modulationofproinflammatoryil6transsignalingaxisbyspliceswitchingoligonucleotidesasatherapeuticmodalityininflammation
AT turunenjanne modulationofproinflammatoryil6transsignalingaxisbyspliceswitchingoligonucleotidesasatherapeuticmodalityininflammation
AT odonovanliz modulationofproinflammatoryil6transsignalingaxisbyspliceswitchingoligonucleotidesasatherapeuticmodalityininflammation
AT gaitmichaelj modulationofproinflammatoryil6transsignalingaxisbyspliceswitchingoligonucleotidesasatherapeuticmodalityininflammation
AT elandaloussisamir modulationofproinflammatoryil6transsignalingaxisbyspliceswitchingoligonucleotidesasatherapeuticmodalityininflammation
AT woodmatthewja modulationofproinflammatoryil6transsignalingaxisbyspliceswitchingoligonucleotidesasatherapeuticmodalityininflammation