Echinococcus multilocularis delta/notch signalling components are expressed in post-mitotic cells.
Autor: | Speicher C; Institute of Hygiene and Microbiology, University of Würzburg, Josef-Schneider-Strasse 2, 97080, Würzburg, Germany., Bergmann M; Institute of Hygiene and Microbiology, University of Würzburg, Josef-Schneider-Strasse 2, 97080, Würzburg, Germany., Brehm K; Institute of Hygiene and Microbiology, University of Würzburg, Josef-Schneider-Strasse 2, 97080, Würzburg, Germany. klaus.brehm@uni-wuerzburg.de. |
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Jazyk: | angličtina |
Zdroj: | Parasitology research [Parasitol Res] 2024 Dec 23; Vol. 123 (12), pp. 418. Date of Electronic Publication: 2024 Dec 23. |
DOI: | 10.1007/s00436-024-08442-4 |
Abstrakt: | Pluripotent somatic stem cells are the drivers of unlimited growth of Echinococcus multilocularis metacestode tissue within the organs of the intermediate host. To understand the dynamics of parasite proliferation within the host, it is therefore important to delineate basic mechanisms of Echinococcus stem cell maintenance and differentiation. We herein undertake the first step towards characterizing the role of an evolutionarily old metazoan cell-cell communication system, delta/notch signalling, in Echinococcus cell fate decisions. Bioinformatic analyses revealed that all central components of this pathway are encoded by the Echinococcus genome and are expressed in parasite larval stages. By in situ hybridisation, we analyzed the expression patterns of clearly identified delta-like ligands, delta1 and delta2, as well as two notch receptors, notch1 and notch2, in metacestode tissue. Except for delta1, which is not expressed in the metacestode, all other components are expressed in distinct cells throughout the parasite's germinal layer. Combined in situ hybridisation and EdU incorporation experiments together with pulse-chase assays further indicate that delta2, notch1, and notch2 are exclusively expressed in post-mitotic cells. Echinococcus asymmetric stem cell division, leading to the progeny of different fates, therefore most probably not involves delta/notch signalling components. Our analyses are relevant for understanding the interplay of fate-determining signalling pathways in Echinococcus cell differentiation and form a basis for further experiments into the role of delta/notch signalling in parasite development. Competing Interests: Declarations. Ethical approval: All animal experiments were carried out in accordance with European and German regulations on the protection of animals (Tierschutzgesetz, Sect. 6). Ethical approval of the study was obtained by the local ethics committee of the government of Lower Franconia (permit no. 55.2–2531.2–1824). Consent to participate: Not applicable. Consent for publication: Not applicable. Competing interests: The authors declare no competing interests. (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.) |
Databáze: | MEDLINE |
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