多房棘球绦虫δ /notch信号成分在有丝分裂后细胞中表达。

IF 1.8 3区 医学 Q2 PARASITOLOGY Parasitology Research Pub Date : 2024-12-23 DOI:10.1007/s00436-024-08442-4
Chris Speicher, Monika Bergmann, Klaus Brehm
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引用次数: 0

摘要

多能体细胞干细胞是多房棘球蚴在中间宿主器官内无限生长的驱动因子。因此,为了了解寄生虫在宿主内增殖的动力学,阐明棘球蚴干细胞维持和分化的基本机制是很重要的。我们在此进行了第一步,以表征一个进化上古老的后生动物细胞-细胞通信系统,δ /notch信号,在棘球蚴细胞命运决定中的作用。生物信息学分析表明,该途径的所有核心成分都由棘球蚴基因组编码,并在寄生虫幼虫阶段表达。通过原位杂交,我们分析了明确鉴定的delta样配体delta1和delta2以及两个缺口受体notch1和notch2在跖骨组织中的表达模式。除了delta1不在后生细胞中表达外,所有其他成分都在寄生虫生发层的不同细胞中表达。结合原位杂交和EdU掺入实验以及脉冲追踪实验进一步表明,delta2、notch1和notch2只在有丝分裂后的细胞中表达。棘球蚴不对称干细胞分裂,导致后代命运不同,因此很可能不涉及δ /notch信号成分。我们的分析有助于理解棘球蚴细胞分化过程中决定命运的信号通路的相互作用,并为进一步研究δ /notch信号通路在寄生虫发育中的作用奠定基础。
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Echinococcus multilocularis delta/notch signalling components are expressed in post-mitotic cells.

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.

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来源期刊
Parasitology Research
Parasitology Research 医学-寄生虫学
CiteScore
4.10
自引率
5.00%
发文量
346
审稿时长
6 months
期刊介绍: The journal Parasitology Research covers the latest developments in parasitology across a variety of disciplines, including biology, medicine and veterinary medicine. Among many topics discussed are chemotherapy and control of parasitic disease, and the relationship of host and parasite. Other coverage includes: Protozoology, Helminthology, Entomology; Morphology (incl. Pathomorphology, Ultrastructure); Biochemistry, Physiology including Pathophysiology; Parasite-Host-Relationships including Immunology and Host Specificity; life history, ecology and epidemiology; and Diagnosis, Chemotherapy and Control of Parasitic Diseases.
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