Extracellular Vesicles Derived From Regenerating Tissue Promote Stem Cell Proliferation in the Planarian Schmidtea mediterranea

Priscilla N. Avalos Najera, Lily L. Wong, David J. Forsthoefel
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Abstract

Extracellular vesicles (EVs) are secreted nanoparticles composed of a lipid bilayer that carry lipid, protein, and nucleic acid cargo between cells as a mode of intercellular communication. Although EVs can promote tissue repair in mammals, their roles in animals with greater regenerative capacity are not well understood. Planarian flatworms are capable of whole-body regeneration due to pluripotent somatic stem cells called neoblasts that proliferate in response to injury. Here, using transmission electron microscopy, nanoparticle tracking analysis, and protein content examination, we showed that EVs enriched from the tissues of the planarian Schmidtea mediterranea had similar morphology and size as other eukaryotic EVs, and that these EVs carried orthologs of the conserved EV biogenesis regulators ALIX and TSG101. PKH67-labeled EVs were taken up efficiently by planarian cells, including S/G2 neoblasts, G1 neoblasts/early progeny, and differentiated cells. When injected into living planarians, EVs from regenerating tissue fragments enhanced the upregulation of neoblast-enriched and proliferation-related transcripts. In addition, EV injection increased the number of F-ara-EdU-labelled cells by 49% as compared to buffer injection only. Our findings demonstrate that regenerating planarians produce EVs that promote stem cell proliferation, and suggest the planarian as an amenable in vivo model for the study of EV function during regeneration.

Abstract Image

再生组织产生的细胞外囊泡促进地中海施米德涡虫干细胞增殖
细胞外囊泡(EVs)是由脂质双层组成的分泌纳米颗粒,作为细胞间通讯的一种模式,在细胞间携带脂质、蛋白质和核酸货物。虽然ev可以促进哺乳动物的组织修复,但它们在具有更大再生能力的动物中的作用尚不清楚。涡虫扁虫能够全身再生,这是由于多能体细胞干细胞(称为新细胞)对损伤的反应增殖。通过透射电镜、纳米颗粒跟踪分析和蛋白质含量检测,研究人员发现从地中海施米德原虫组织中富集的EV与其他真核EV具有相似的形态和大小,并且这些EV携带保守的EV生物发生调节因子ALIX和TSG101的同源物。pkh67标记的ev被涡虫细胞(包括S/G2新生细胞、G1新生细胞/早期后代细胞和分化细胞)高效吸收。当注入活体涡虫体内时,来自再生组织片段的ev增强了新母细胞富集和增殖相关转录本的上调。此外,与仅注射缓冲液相比,EV注射使f -ara- edu标记的细胞数量增加了49%。我们的研究结果表明,再生涡虫产生的EV促进干细胞增殖,并表明涡虫是研究再生过程中EV功能的合适体内模型。
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