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      Posterior regeneration in Isodiametra pulchra (Acoela, Acoelomorpha)

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          Abstract

          Introduction

          Regeneration is a widespread phenomenon in the animal kingdom, but the capacity to restore damaged or missing tissue varies greatly between different phyla and even within the same phylum. However, the distantly related Acoelomorpha and Platyhelminthes share a strikingly similar stem-cell system and regenerative capacity. Therefore, comparing the underlying mechanisms in these two phyla paves the way for an increased understanding of the evolution of this developmental process.

          To date, Isodiametra pulchra is the most promising candidate as a model for the Acoelomorpha, as it reproduces steadily under laboratory conditions and is amenable to various techniques, including the silencing of gene expression by RNAi. In order to provide an essential framework for future studies, we report the succession of regeneration events via the use of cytochemical, histological and microscopy techniques, and specify the total number of cells in adult individuals.

          Results

          Isodiametra pulchra is not capable of regenerating a new head, but completely restores all posterior structures within 10 days. Following amputation, the wound closes via the contraction of local muscle fibres and an extension of the dorsal epidermis. Subsequently, stem cells and differentiating cells invade the wound area and form a loosely delimited blastema. After two days, the posterior end is re-patterned with the male (and occasionally the female) genital primordium being apparent. Successively, these primordia differentiate into complete copulatory organs. The size of the body and also of the male and female copulatory organs, as well as the distance between the copulatory organs, progressively increase and by nine days copulation is possible. Adult individuals with an average length of 670 μm consist of approximately 8100 cells.

          Conclusion

          Isodiametra pulchra regenerates through a combination of morphallactic and epimorphic processes. Existing structures are “re-modelled” and provide a framework onto which newly differentiating cells are added. Growth proceeds through the intercalary addition of structures, mirroring the embryonic and post-embryonic development of various organ systems. The suitability of Isodiametra pulchra for laboratory techniques, the fact that its transcriptome and genome data will soon be available, as well as its small size and low number of cells, make it a prime candidate subject for research into the cellular mechanisms that underlie regeneration in acoelomorphs.

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          Most cited references41

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          A low-viscosity epoxy resin embedding medium for electron microscopy.

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            Embedding in epoxy resins for ultrathin sectioning in electron microscopy.

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              Evolution of animal regeneration: re-emergence of a field.

              Regeneration, the replacement of lost body parts, is widespread yet highly variable among animals. Explaining this variation remains a major challenge in biology. Great strides have been made in understanding the phylogenetic distribution, ecological context and developmental basis of regeneration, and these new data are yielding novel insights into why and how regeneration evolves. Here, we review the phylogenetic distribution of regeneration and discuss how the origin, maintenance and loss of regeneration can each be driven by distinct factors. As the complexity of factors affecting regeneration evolution is increasingly appreciated, and as explicitly evolutionary studies of regeneration become more common, the coming years promise exciting progress in revealing the underlying mechanisms that have shaped animal regeneration.
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                Author and article information

                Journal
                Front Zool
                Front. Zool
                Frontiers in Zoology
                BioMed Central
                1742-9994
                2013
                28 October 2013
                : 10
                : 64
                Affiliations
                [1 ]Department of Genetics, University of Barcelona, Av. Diagonal 643, edifici annex, planta 2a, 08028 Barcelona, Spain
                [2 ]Department of Evolutionary Developmental Biology, University of Innsbruck, Technikerstrasse 25, 6020 Innsbruck, Austria
                [3 ]Department of Genetics, Evolution and Environment, University College London, Darwin Building, Gower Street, London WC1E 6BT, UK
                [4 ]Department of Integrative Zoology, University of Vienna, Althanstrasse 14, UZA 1, 1090 Vienna, Austria
                [5 ]Institució Catalana de Recerca i Estudis Avançats (ICREA), Passeig Lluís Companys 23, 08010 Barcelona, Spain
                Article
                1742-9994-10-64
                10.1186/1742-9994-10-64
                3816570
                24160844
                7650c99c-22e6-4567-b876-297469a7f865
                Copyright ©2013 Perea-Atienza et al.; licensee BioMed Central Ltd.

                This is an open access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 15 April 2013
                : 17 October 2013
                Categories
                Research

                Animal science & Zoology
                stem cell,neoblast,copulatory organ,epimorphosis,morphallaxis
                Animal science & Zoology
                stem cell, neoblast, copulatory organ, epimorphosis, morphallaxis

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