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A pan‐metazoan concept for adult stem cells: the wobbling Penrose landscape

Adult stem cells (ASCs) in vertebrates and model invertebrates (e.g. Drosophila melanogaster) are typically long‐lived, lineage‐restricted, clonogenic and quiescent cells with somatic descendants and tissue/organ‐restricted activities. Such ASCs are mostly rare, morphologically undifferentiated, and...

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Autores principales: Rinkevich, Baruch, Ballarin, Loriano, Martinez, Pedro, Somorjai, Ildiko, Ben‐Hamo, Oshrat, Borisenko, Ilya, Berezikov, Eugene, Ereskovsky, Alexander, Gazave, Eve, Khnykin, Denis, Manni, Lucia, Petukhova, Olga, Rosner, Amalia, Röttinger, Eric, Spagnuolo, Antonietta, Sugni, Michela, Tiozzo, Stefano, Hobmayer, Bert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292022/
https://www.ncbi.nlm.nih.gov/pubmed/34617397
http://dx.doi.org/10.1111/brv.12801
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author Rinkevich, Baruch
Ballarin, Loriano
Martinez, Pedro
Somorjai, Ildiko
Ben‐Hamo, Oshrat
Borisenko, Ilya
Berezikov, Eugene
Ereskovsky, Alexander
Gazave, Eve
Khnykin, Denis
Manni, Lucia
Petukhova, Olga
Rosner, Amalia
Röttinger, Eric
Spagnuolo, Antonietta
Sugni, Michela
Tiozzo, Stefano
Hobmayer, Bert
author_facet Rinkevich, Baruch
Ballarin, Loriano
Martinez, Pedro
Somorjai, Ildiko
Ben‐Hamo, Oshrat
Borisenko, Ilya
Berezikov, Eugene
Ereskovsky, Alexander
Gazave, Eve
Khnykin, Denis
Manni, Lucia
Petukhova, Olga
Rosner, Amalia
Röttinger, Eric
Spagnuolo, Antonietta
Sugni, Michela
Tiozzo, Stefano
Hobmayer, Bert
author_sort Rinkevich, Baruch
collection PubMed
description Adult stem cells (ASCs) in vertebrates and model invertebrates (e.g. Drosophila melanogaster) are typically long‐lived, lineage‐restricted, clonogenic and quiescent cells with somatic descendants and tissue/organ‐restricted activities. Such ASCs are mostly rare, morphologically undifferentiated, and undergo asymmetric cell division. Characterized by ‘stemness’ gene expression, they can regulate tissue/organ homeostasis, repair and regeneration. By contrast, analysis of other animal phyla shows that ASCs emerge at different life stages, present both differentiated and undifferentiated phenotypes, and may possess amoeboid movement. Usually pluri/totipotent, they may express germ‐cell markers, but often lack germ‐line sequestering, and typically do not reside in discrete niches. ASCs may constitute up to 40% of animal cells, and participate in a range of biological phenomena, from whole‐body regeneration, dormancy, and agametic asexual reproduction, to indeterminate growth. They are considered legitimate units of selection. Conceptualizing this divergence, we present an alternative stemness metaphor to the Waddington landscape: the ‘wobbling Penrose’ landscape. Here, totipotent ASCs adopt ascending/descending courses of an ‘Escherian stairwell’, in a lifelong totipotency pathway. ASCs may also travel along lower stemness echelons to reach fully differentiated states. However, from any starting state, cells can change their stemness status, underscoring their dynamic cellular potencies. Thus, vertebrate ASCs may reflect just one metazoan ASC archetype.
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spelling pubmed-92920222022-07-20 A pan‐metazoan concept for adult stem cells: the wobbling Penrose landscape Rinkevich, Baruch Ballarin, Loriano Martinez, Pedro Somorjai, Ildiko Ben‐Hamo, Oshrat Borisenko, Ilya Berezikov, Eugene Ereskovsky, Alexander Gazave, Eve Khnykin, Denis Manni, Lucia Petukhova, Olga Rosner, Amalia Röttinger, Eric Spagnuolo, Antonietta Sugni, Michela Tiozzo, Stefano Hobmayer, Bert Biol Rev Camb Philos Soc Original Articles Adult stem cells (ASCs) in vertebrates and model invertebrates (e.g. Drosophila melanogaster) are typically long‐lived, lineage‐restricted, clonogenic and quiescent cells with somatic descendants and tissue/organ‐restricted activities. Such ASCs are mostly rare, morphologically undifferentiated, and undergo asymmetric cell division. Characterized by ‘stemness’ gene expression, they can regulate tissue/organ homeostasis, repair and regeneration. By contrast, analysis of other animal phyla shows that ASCs emerge at different life stages, present both differentiated and undifferentiated phenotypes, and may possess amoeboid movement. Usually pluri/totipotent, they may express germ‐cell markers, but often lack germ‐line sequestering, and typically do not reside in discrete niches. ASCs may constitute up to 40% of animal cells, and participate in a range of biological phenomena, from whole‐body regeneration, dormancy, and agametic asexual reproduction, to indeterminate growth. They are considered legitimate units of selection. Conceptualizing this divergence, we present an alternative stemness metaphor to the Waddington landscape: the ‘wobbling Penrose’ landscape. Here, totipotent ASCs adopt ascending/descending courses of an ‘Escherian stairwell’, in a lifelong totipotency pathway. ASCs may also travel along lower stemness echelons to reach fully differentiated states. However, from any starting state, cells can change their stemness status, underscoring their dynamic cellular potencies. Thus, vertebrate ASCs may reflect just one metazoan ASC archetype. Blackwell Publishing Ltd 2021-10-06 2022-02 /pmc/articles/PMC9292022/ /pubmed/34617397 http://dx.doi.org/10.1111/brv.12801 Text en © 2021 The Authors. Biological Reviews published by John Wiley & Sons Ltd on behalf of Cambridge Philosophical Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Rinkevich, Baruch
Ballarin, Loriano
Martinez, Pedro
Somorjai, Ildiko
Ben‐Hamo, Oshrat
Borisenko, Ilya
Berezikov, Eugene
Ereskovsky, Alexander
Gazave, Eve
Khnykin, Denis
Manni, Lucia
Petukhova, Olga
Rosner, Amalia
Röttinger, Eric
Spagnuolo, Antonietta
Sugni, Michela
Tiozzo, Stefano
Hobmayer, Bert
A pan‐metazoan concept for adult stem cells: the wobbling Penrose landscape
title A pan‐metazoan concept for adult stem cells: the wobbling Penrose landscape
title_full A pan‐metazoan concept for adult stem cells: the wobbling Penrose landscape
title_fullStr A pan‐metazoan concept for adult stem cells: the wobbling Penrose landscape
title_full_unstemmed A pan‐metazoan concept for adult stem cells: the wobbling Penrose landscape
title_short A pan‐metazoan concept for adult stem cells: the wobbling Penrose landscape
title_sort pan‐metazoan concept for adult stem cells: the wobbling penrose landscape
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292022/
https://www.ncbi.nlm.nih.gov/pubmed/34617397
http://dx.doi.org/10.1111/brv.12801
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