Extracellular Vesicles Derived From Regenerating Tissue Promote Stem Cell Proliferation in the Planarian <i>Schmidtea mediterranea</i>

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 <i>Schmidtea mediterranea</i> 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 <i>F-ara</i>-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.

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Publication Details

Journal
Journal of Extracellular Biology
Published
2025-03-01
DOI
https://doi.org/10.1002/jex2.70040
Citations
4
Primary Topic
Planarian Biology and Electrostimulation
Type
article
Field-Weighted Citation Impact
3.22

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article

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

Priscilla N. Avalos, David J. Forsthoefel, Lily Wong
4 citations
Journal of Extracellular Biology
Planarian Biology and Electrostimulation
3.22
article

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

Priscilla N. Avalos, David J. Forsthoefel, Lily Wong
article en
4 citations

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 <i>Schmidtea mediterranea</i> 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 <i>F-ara</i>-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.

Journal of Extracellular BiologyVol. 4(3)
Oklahoma Medical Research Foundation (US), University of Oklahoma Health Sciences Center (US)
National Institute of General Medical Sciences
Life in Land
Openalex Percentile: Top 9%
Planarian Biology and Electrostimulation
3.22
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