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In vitro evaluation of the effect of galectins on Schistosoma mansoni motility

OBJECTIVE: Galectins are sugar-binding proteins that participate in many biological processes, such as immunity, by regulating host immune cells and their direct interaction with pathogens. They are involved in mediating infection by Schistosoma mansoni, a parasitic trematode that causes schistosomi...

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Autores principales: Takeuchi, Tomoharu, Nakamura, Risa, Hamasaki, Megumi, Oyama, Midori, Hamano, Shinjiro, Hatanaka, Tomomi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10566010/
https://www.ncbi.nlm.nih.gov/pubmed/37817269
http://dx.doi.org/10.1186/s13104-023-06530-9
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author Takeuchi, Tomoharu
Nakamura, Risa
Hamasaki, Megumi
Oyama, Midori
Hamano, Shinjiro
Hatanaka, Tomomi
author_facet Takeuchi, Tomoharu
Nakamura, Risa
Hamasaki, Megumi
Oyama, Midori
Hamano, Shinjiro
Hatanaka, Tomomi
author_sort Takeuchi, Tomoharu
collection PubMed
description OBJECTIVE: Galectins are sugar-binding proteins that participate in many biological processes, such as immunity, by regulating host immune cells and their direct interaction with pathogens. They are involved in mediating infection by Schistosoma mansoni, a parasitic trematode that causes schistosomiasis. However, their direct effects on schistosomes have not been investigated. RESULTS: We found that galectin-2 recognizes S. mansoni glycoconjugates and investigated whether galectin-1, 2, and 3 can directly affect S. mansoni in vitro. Adult S. mansoni were treated with recombinant galectin-1, 2, and 3 proteins or praziquantel, a positive control. Treatment with galectin-1, 2, and 3 had no significant effect on S. mansoni motility, and no other differences were observed under a stereoscopic microscope. Hence, galectin-1, 2, and 3 may have a little direct effect on S. mansoni. However, they might play a role in the infection in vivo via the modulation of the host immune response or secretory molecules from S. mansoni. To the best of our knowledge, this is the first study to investigate the direct effect of galectins on S. mansoni and helps in understanding the roles of galectins in S. mansoni infection in vivo. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-023-06530-9.
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spelling pubmed-105660102023-10-12 In vitro evaluation of the effect of galectins on Schistosoma mansoni motility Takeuchi, Tomoharu Nakamura, Risa Hamasaki, Megumi Oyama, Midori Hamano, Shinjiro Hatanaka, Tomomi BMC Res Notes Research Note OBJECTIVE: Galectins are sugar-binding proteins that participate in many biological processes, such as immunity, by regulating host immune cells and their direct interaction with pathogens. They are involved in mediating infection by Schistosoma mansoni, a parasitic trematode that causes schistosomiasis. However, their direct effects on schistosomes have not been investigated. RESULTS: We found that galectin-2 recognizes S. mansoni glycoconjugates and investigated whether galectin-1, 2, and 3 can directly affect S. mansoni in vitro. Adult S. mansoni were treated with recombinant galectin-1, 2, and 3 proteins or praziquantel, a positive control. Treatment with galectin-1, 2, and 3 had no significant effect on S. mansoni motility, and no other differences were observed under a stereoscopic microscope. Hence, galectin-1, 2, and 3 may have a little direct effect on S. mansoni. However, they might play a role in the infection in vivo via the modulation of the host immune response or secretory molecules from S. mansoni. To the best of our knowledge, this is the first study to investigate the direct effect of galectins on S. mansoni and helps in understanding the roles of galectins in S. mansoni infection in vivo. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-023-06530-9. BioMed Central 2023-10-10 /pmc/articles/PMC10566010/ /pubmed/37817269 http://dx.doi.org/10.1186/s13104-023-06530-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Note
Takeuchi, Tomoharu
Nakamura, Risa
Hamasaki, Megumi
Oyama, Midori
Hamano, Shinjiro
Hatanaka, Tomomi
In vitro evaluation of the effect of galectins on Schistosoma mansoni motility
title In vitro evaluation of the effect of galectins on Schistosoma mansoni motility
title_full In vitro evaluation of the effect of galectins on Schistosoma mansoni motility
title_fullStr In vitro evaluation of the effect of galectins on Schistosoma mansoni motility
title_full_unstemmed In vitro evaluation of the effect of galectins on Schistosoma mansoni motility
title_short In vitro evaluation of the effect of galectins on Schistosoma mansoni motility
title_sort in vitro evaluation of the effect of galectins on schistosoma mansoni motility
topic Research Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10566010/
https://www.ncbi.nlm.nih.gov/pubmed/37817269
http://dx.doi.org/10.1186/s13104-023-06530-9
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