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Apoptotic bodies in phytoplankton suggest evolutionary conservation of cell death mechanisms
Umeå University, Faculty of Science and Technology, Department of Chemistry. Department of Food, Environmental and Nutritional Sciences, University of Milan, Milan, Italy.
Umeå University, Faculty of Science and Technology, Department of Chemistry.
Umeå Plant Science Centre (UPSC), Department of Forest Genetics and Plant Physiology, Swedish University of Agricultural Sciences, Umeå, Sweden.
Umeå Plant Science Centre (UPSC), Department of Forest Genetics and Plant Physiology, Swedish University of Agricultural Sciences, Umeå, Sweden.
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2025 (English)In: Nature Communications, E-ISSN 2041-1723, Vol. 16, no 1, article id 8427Article in journal (Refereed) Published
Abstract [en]

Programmed Cell Death (PCD) in eukaryotes is a regulated process occurring during development, cell differentiation and aging. Apoptosis is a particularly well studied morphotype of PCD, only observed in animal cells (metazoan). Its most definitive hallmark is the formation and release of membrane-enclosed extracellular vesicles called Apoptotic Bodies (ABs). Although apoptotic-like features have been described in plants, yeast, protozoa and phytoplankton, the production of ABs has been thought to be limited to multicellular animals. Here we report the production and release of extracellular ABs in a non-metazoan unicellular eukaryote, the cryptophyte alga Guillardia theta. Morphologies of G. theta cells during aging and pharmacologically-induced cell death confirm the presence of ABs and apoptosis in phytoplankton. G. theta ABs have similar composition to metazoan ABs, carrying DNA, proteins, lipids, carbohydrates, fragments of organelles and cytosol portions. Our results demonstrate that G. theta, a microalga that arose from secondary endosymbiosis, experiences apoptotic cell death in physiological conditions, similar to animal cells. Since secondary endosymbiosis occurred prior to the origin of multicellularity, our discovery questions the evolutionary origin of PCD.

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Springer Nature, 2025. Vol. 16, no 1, article id 8427
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Cell Biology
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URN: urn:nbn:se:umu:diva-245353DOI: 10.1038/s41467-025-63956-4ISI: 001581141900004PubMedID: 40998840Scopus ID: 2-s2.0-105017184893OAI: oai:DiVA.org:umu-245353DiVA, id: diva2:2005529
Available from: 2025-10-10 Created: 2025-10-10 Last updated: 2025-10-10Bibliographically approved

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Corredor, LuisaVergou, Georgia AntoniaWheaton, Benjamin J.Gorzsás, AndrásFunk, Christiane

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Corredor, LuisaVergou, Georgia AntoniaWheaton, Benjamin J.Gorzsás, AndrásFunk, Christiane
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Department of ChemistryDepartment of Medical and Translational Biology
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