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A designer hyper interleukin 11 (H11) is a biologically active cytokine

BACKGROUND: Interleukin 11 (IL-11) is a pleiotropic cytokine with anti-apoptotic, anti-inflammatory and hematopoietic potential. The IL-11 activity is determined by the expression of the IL-11R receptor alpha (IL-11Rα) and the signal transducing subunit β (gp130) on the cell membrane. A recombinant...

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Autores principales: Dams-Kozlowska, Hanna, Gryska, Katarzyna, Kwiatkowska-Borowczyk, Eliza, Izycki, Dariusz, Rose-John, Stefan, Mackiewicz, Andrzej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382428/
https://www.ncbi.nlm.nih.gov/pubmed/22433466
http://dx.doi.org/10.1186/1472-6750-12-8
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author Dams-Kozlowska, Hanna
Gryska, Katarzyna
Kwiatkowska-Borowczyk, Eliza
Izycki, Dariusz
Rose-John, Stefan
Mackiewicz, Andrzej
author_facet Dams-Kozlowska, Hanna
Gryska, Katarzyna
Kwiatkowska-Borowczyk, Eliza
Izycki, Dariusz
Rose-John, Stefan
Mackiewicz, Andrzej
author_sort Dams-Kozlowska, Hanna
collection PubMed
description BACKGROUND: Interleukin 11 (IL-11) is a pleiotropic cytokine with anti-apoptotic, anti-inflammatory and hematopoietic potential. The IL-11 activity is determined by the expression of the IL-11R receptor alpha (IL-11Rα) and the signal transducing subunit β (gp130) on the cell membrane. A recombinant soluble form of the IL-11Rα (sIL-11Rα) in combination with IL-11 acts as an agonist on cells expressing the gp130 molecule. We constructed a designer cytokine Hyper IL-11 (H11), which is exclusively composed of naturally existing components. It contains the full length sIL-11Rα connected with the mature IL-11 protein using their natural sequences only. Such a construct has two major advantages: (i) its components are as close as possible to the natural forms of both proteins and (ii) it lacks an artificial linker what should avoid induction of antibody production. RESULTS: The H11 construct was generated, the protein was produced in a baculovirus expression system and was then purified by using ion exchange chromatography. The H11 protein displayed activity in three independent bioassays, (i) it induced acute phase proteins production in HepG2 cells expressing IL-11, IL-11Rα and gp130, (ii) it stimulated the proliferation of B9 cells (cells expressing IL-11Rα and gp130) and (iii) proliferation of Baf/3-gp130 cells (cells not expressing IL-11 and IL-11Rα but gp130). Moreover, the preliminary data indicated that H11 was functionally distinct from Hyper-IL-6, a molecule which utilizes the same homodimer of signal transducing receptor (gp130). CONCLUSIONS: The biologically active H11 may be potentially useful for treatment of thrombocytopenia, infertility, multiple sclerosis, cardiovascular diseases or inflammatory disorders.
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spelling pubmed-33824282012-06-26 A designer hyper interleukin 11 (H11) is a biologically active cytokine Dams-Kozlowska, Hanna Gryska, Katarzyna Kwiatkowska-Borowczyk, Eliza Izycki, Dariusz Rose-John, Stefan Mackiewicz, Andrzej BMC Biotechnol Research Article BACKGROUND: Interleukin 11 (IL-11) is a pleiotropic cytokine with anti-apoptotic, anti-inflammatory and hematopoietic potential. The IL-11 activity is determined by the expression of the IL-11R receptor alpha (IL-11Rα) and the signal transducing subunit β (gp130) on the cell membrane. A recombinant soluble form of the IL-11Rα (sIL-11Rα) in combination with IL-11 acts as an agonist on cells expressing the gp130 molecule. We constructed a designer cytokine Hyper IL-11 (H11), which is exclusively composed of naturally existing components. It contains the full length sIL-11Rα connected with the mature IL-11 protein using their natural sequences only. Such a construct has two major advantages: (i) its components are as close as possible to the natural forms of both proteins and (ii) it lacks an artificial linker what should avoid induction of antibody production. RESULTS: The H11 construct was generated, the protein was produced in a baculovirus expression system and was then purified by using ion exchange chromatography. The H11 protein displayed activity in three independent bioassays, (i) it induced acute phase proteins production in HepG2 cells expressing IL-11, IL-11Rα and gp130, (ii) it stimulated the proliferation of B9 cells (cells expressing IL-11Rα and gp130) and (iii) proliferation of Baf/3-gp130 cells (cells not expressing IL-11 and IL-11Rα but gp130). Moreover, the preliminary data indicated that H11 was functionally distinct from Hyper-IL-6, a molecule which utilizes the same homodimer of signal transducing receptor (gp130). CONCLUSIONS: The biologically active H11 may be potentially useful for treatment of thrombocytopenia, infertility, multiple sclerosis, cardiovascular diseases or inflammatory disorders. BioMed Central 2012-03-21 /pmc/articles/PMC3382428/ /pubmed/22433466 http://dx.doi.org/10.1186/1472-6750-12-8 Text en Copyright ©2012 Dams-Kozlowska et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Dams-Kozlowska, Hanna
Gryska, Katarzyna
Kwiatkowska-Borowczyk, Eliza
Izycki, Dariusz
Rose-John, Stefan
Mackiewicz, Andrzej
A designer hyper interleukin 11 (H11) is a biologically active cytokine
title A designer hyper interleukin 11 (H11) is a biologically active cytokine
title_full A designer hyper interleukin 11 (H11) is a biologically active cytokine
title_fullStr A designer hyper interleukin 11 (H11) is a biologically active cytokine
title_full_unstemmed A designer hyper interleukin 11 (H11) is a biologically active cytokine
title_short A designer hyper interleukin 11 (H11) is a biologically active cytokine
title_sort designer hyper interleukin 11 (h11) is a biologically active cytokine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382428/
https://www.ncbi.nlm.nih.gov/pubmed/22433466
http://dx.doi.org/10.1186/1472-6750-12-8
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