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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2013
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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. |
format | Online Article Text |
id | pubmed-3714392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
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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