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Transforming growth factor-β signalling regulates protoscolex formation in the Echinococcus multilocularis metacestode
The lethal zoonosis alveolar echinococcosis (AE) is caused by tumor-like, infiltrative growth of the metacestode larval stage of the tapeworm Echinococcus multilocularis. We previously showed that the metacestode is composed of posteriorized tissue and that the production of the subsequent larval st...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073696/ https://www.ncbi.nlm.nih.gov/pubmed/37033489 http://dx.doi.org/10.3389/fcimb.2023.1153117 |
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author | Kaethner, Marc Epping, Kerstin Bernthaler, Peter Rudolf, Kilian Thomann, Irena Leitschuh, Nadine Bergmann, Monika Spiliotis, Markus Koziol, Uriel Brehm, Klaus |
author_facet | Kaethner, Marc Epping, Kerstin Bernthaler, Peter Rudolf, Kilian Thomann, Irena Leitschuh, Nadine Bergmann, Monika Spiliotis, Markus Koziol, Uriel Brehm, Klaus |
author_sort | Kaethner, Marc |
collection | PubMed |
description | The lethal zoonosis alveolar echinococcosis (AE) is caused by tumor-like, infiltrative growth of the metacestode larval stage of the tapeworm Echinococcus multilocularis. We previously showed that the metacestode is composed of posteriorized tissue and that the production of the subsequent larval stage, the protoscolex, depends on re-establishment of anterior identities within the metacestode germinative layer. It is, however, unclear so far how protoscolex differentiation in Echinococcus is regulated. We herein characterized the full complement of E. multilocularis TGFβ/BMP receptors, which is composed of one type II and three type I receptor serine/threonine kinases. Functional analyzes showed that all Echinococcus TGFβ/BMP receptors are enzymatically active and respond to host derived TGFβ/BMP ligands for activating downstream Smad transcription factors. In situ hybridization experiments demonstrated that the Echinococcus TGFβ/BMP receptors are mainly expressed by nerve and muscle cells within the germinative layer and in developing brood capsules. Interestingly, the production of brood capsules, which later give rise to protoscoleces, was strongly suppressed in the presence of inhibitors directed against TGFβ/BMP receptors, whereas protoscolex differentiation was accelerated in response to host BMP2 and TGFβ. Apart from being responsive to host TGFβ/BMP ligands, protoscolex production also correlated with the expression of a parasite-derived TGFβ-like ligand, EmACT, which is expressed in early brood capsules and which is strongly expressed in anterior domains during protoscolex development. Taken together, these data indicate an important role of TGFβ/BMP signalling in Echinococcus anterior pole formation and protoscolex development. Since TGFβ is accumulating around metacestode lesions at later stages of the infection, the host immune response could thus serve as a signal by which the parasite senses the time point at which protoscoleces must be produced. Overall, our data shed new light on molecular mechanisms of host-parasite interaction during AE and are relevant for the development of novel treatment strategies. |
format | Online Article Text |
id | pubmed-10073696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100736962023-04-06 Transforming growth factor-β signalling regulates protoscolex formation in the Echinococcus multilocularis metacestode Kaethner, Marc Epping, Kerstin Bernthaler, Peter Rudolf, Kilian Thomann, Irena Leitschuh, Nadine Bergmann, Monika Spiliotis, Markus Koziol, Uriel Brehm, Klaus Front Cell Infect Microbiol Cellular and Infection Microbiology The lethal zoonosis alveolar echinococcosis (AE) is caused by tumor-like, infiltrative growth of the metacestode larval stage of the tapeworm Echinococcus multilocularis. We previously showed that the metacestode is composed of posteriorized tissue and that the production of the subsequent larval stage, the protoscolex, depends on re-establishment of anterior identities within the metacestode germinative layer. It is, however, unclear so far how protoscolex differentiation in Echinococcus is regulated. We herein characterized the full complement of E. multilocularis TGFβ/BMP receptors, which is composed of one type II and three type I receptor serine/threonine kinases. Functional analyzes showed that all Echinococcus TGFβ/BMP receptors are enzymatically active and respond to host derived TGFβ/BMP ligands for activating downstream Smad transcription factors. In situ hybridization experiments demonstrated that the Echinococcus TGFβ/BMP receptors are mainly expressed by nerve and muscle cells within the germinative layer and in developing brood capsules. Interestingly, the production of brood capsules, which later give rise to protoscoleces, was strongly suppressed in the presence of inhibitors directed against TGFβ/BMP receptors, whereas protoscolex differentiation was accelerated in response to host BMP2 and TGFβ. Apart from being responsive to host TGFβ/BMP ligands, protoscolex production also correlated with the expression of a parasite-derived TGFβ-like ligand, EmACT, which is expressed in early brood capsules and which is strongly expressed in anterior domains during protoscolex development. Taken together, these data indicate an important role of TGFβ/BMP signalling in Echinococcus anterior pole formation and protoscolex development. Since TGFβ is accumulating around metacestode lesions at later stages of the infection, the host immune response could thus serve as a signal by which the parasite senses the time point at which protoscoleces must be produced. Overall, our data shed new light on molecular mechanisms of host-parasite interaction during AE and are relevant for the development of novel treatment strategies. Frontiers Media S.A. 2023-03-22 /pmc/articles/PMC10073696/ /pubmed/37033489 http://dx.doi.org/10.3389/fcimb.2023.1153117 Text en Copyright © 2023 Kaethner, Epping, Bernthaler, Rudolf, Thomann, Leitschuh, Bergmann, Spiliotis, Koziol and Brehm https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Kaethner, Marc Epping, Kerstin Bernthaler, Peter Rudolf, Kilian Thomann, Irena Leitschuh, Nadine Bergmann, Monika Spiliotis, Markus Koziol, Uriel Brehm, Klaus Transforming growth factor-β signalling regulates protoscolex formation in the Echinococcus multilocularis metacestode |
title | Transforming growth factor-β signalling regulates protoscolex formation in the Echinococcus multilocularis metacestode |
title_full | Transforming growth factor-β signalling regulates protoscolex formation in the Echinococcus multilocularis metacestode |
title_fullStr | Transforming growth factor-β signalling regulates protoscolex formation in the Echinococcus multilocularis metacestode |
title_full_unstemmed | Transforming growth factor-β signalling regulates protoscolex formation in the Echinococcus multilocularis metacestode |
title_short | Transforming growth factor-β signalling regulates protoscolex formation in the Echinococcus multilocularis metacestode |
title_sort | transforming growth factor-β signalling regulates protoscolex formation in the echinococcus multilocularis metacestode |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073696/ https://www.ncbi.nlm.nih.gov/pubmed/37033489 http://dx.doi.org/10.3389/fcimb.2023.1153117 |
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