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Designer Cytokine Hyper Interleukin 11 (H11) is a Megakaryopoietic Factor

Interleukin-11 (IL-11) displays megakaryopoietic activity. We constructed super-cytokine Hyper- IL11 (H11) by linking soluble IL-11 receptor α (sIL-11Rα) with IL-11, which directly targets β-receptor (gp130) signal transducing subunit. The effects of H11 on hematopoiesis with a focus on megakaryopoi...

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Autores principales: Dams-Kozlowska, Hanna, Kwiatkowska-Borowczyk, Eliza, Gryska, Katarzyna, Mackiewicz, Andrzej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3714392/
https://www.ncbi.nlm.nih.gov/pubmed/23869192
http://dx.doi.org/10.7150/ijms.5638
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author Dams-Kozlowska, Hanna
Kwiatkowska-Borowczyk, Eliza
Gryska, Katarzyna
Mackiewicz, Andrzej
author_facet Dams-Kozlowska, Hanna
Kwiatkowska-Borowczyk, Eliza
Gryska, Katarzyna
Mackiewicz, Andrzej
author_sort Dams-Kozlowska, Hanna
collection PubMed
description Interleukin-11 (IL-11) displays megakaryopoietic activity. We constructed super-cytokine Hyper- IL11 (H11) by linking soluble IL-11 receptor α (sIL-11Rα) with IL-11, which directly targets β-receptor (gp130) signal transducing subunit. The effects of H11 on hematopoiesis with a focus on megakaryopoiesis were studied. The expansion, differentiation and type of colony formation of cord blood progenitor Lin-CD34+ cells were analyzed. H11 was more effective than recombinant human IL-11 (rhIL-11) in enhancement of the Lin-CD34+ cells expansion and differentiation into megakaryocytes (Mk). It induced higher expression of CD41a and CD61 antigens, resulting in a substantially larger population of CD34-CD41a(high)CD61(high) cells. H11 treatment led to increased number of small and mainly medium megakaryocyte colony formation (Mk-CFU). Moreover, it induced the formation of a small number of large colonies, which were not observed following rhIL-11 treatment. Significantly higher number of H11 derived Mk colonies released platelets-like particles (PLP). Furthermore, H11 was considerably more potent than rhIL-11 in promoting differentiation of Lin-CD43+ cells toward erythrocytes. Our results indicate that H11 is more effective than rhIL-11 in enhancing expansion of early progenitors and directing them to megakaryocyte and erythroid cells and in inducing maturation of Mk. Thus, H11 may prove beneficial for thrombocytopenia treatment and/or an ex vivo expansion of megakaryocytes.
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spelling pubmed-37143922013-07-18 Designer Cytokine Hyper Interleukin 11 (H11) is a Megakaryopoietic Factor Dams-Kozlowska, Hanna Kwiatkowska-Borowczyk, Eliza Gryska, Katarzyna Mackiewicz, Andrzej Int J Med Sci Research Paper Interleukin-11 (IL-11) displays megakaryopoietic activity. We constructed super-cytokine Hyper- IL11 (H11) by linking soluble IL-11 receptor α (sIL-11Rα) with IL-11, which directly targets β-receptor (gp130) signal transducing subunit. The effects of H11 on hematopoiesis with a focus on megakaryopoiesis were studied. The expansion, differentiation and type of colony formation of cord blood progenitor Lin-CD34+ cells were analyzed. H11 was more effective than recombinant human IL-11 (rhIL-11) in enhancement of the Lin-CD34+ cells expansion and differentiation into megakaryocytes (Mk). It induced higher expression of CD41a and CD61 antigens, resulting in a substantially larger population of CD34-CD41a(high)CD61(high) cells. H11 treatment led to increased number of small and mainly medium megakaryocyte colony formation (Mk-CFU). Moreover, it induced the formation of a small number of large colonies, which were not observed following rhIL-11 treatment. Significantly higher number of H11 derived Mk colonies released platelets-like particles (PLP). Furthermore, H11 was considerably more potent than rhIL-11 in promoting differentiation of Lin-CD43+ cells toward erythrocytes. Our results indicate that H11 is more effective than rhIL-11 in enhancing expansion of early progenitors and directing them to megakaryocyte and erythroid cells and in inducing maturation of Mk. Thus, H11 may prove beneficial for thrombocytopenia treatment and/or an ex vivo expansion of megakaryocytes. Ivyspring International Publisher 2013-07-09 /pmc/articles/PMC3714392/ /pubmed/23869192 http://dx.doi.org/10.7150/ijms.5638 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Research Paper
Dams-Kozlowska, Hanna
Kwiatkowska-Borowczyk, Eliza
Gryska, Katarzyna
Mackiewicz, Andrzej
Designer Cytokine Hyper Interleukin 11 (H11) is a Megakaryopoietic Factor
title Designer Cytokine Hyper Interleukin 11 (H11) is a Megakaryopoietic Factor
title_full Designer Cytokine Hyper Interleukin 11 (H11) is a Megakaryopoietic Factor
title_fullStr Designer Cytokine Hyper Interleukin 11 (H11) is a Megakaryopoietic Factor
title_full_unstemmed Designer Cytokine Hyper Interleukin 11 (H11) is a Megakaryopoietic Factor
title_short Designer Cytokine Hyper Interleukin 11 (H11) is a Megakaryopoietic Factor
title_sort designer cytokine hyper interleukin 11 (h11) is a megakaryopoietic factor
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3714392/
https://www.ncbi.nlm.nih.gov/pubmed/23869192
http://dx.doi.org/10.7150/ijms.5638
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