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      Cell Turnover and Detritus Production in Marine Sponges from Tropical and Temperate Benthic Ecosystems

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          Abstract

          This study describes in vivo cell turnover (the balance between cell proliferation and cell loss) in eight marine sponge species from tropical coral reef, mangrove and temperate Mediterranean reef ecosystems. Cell proliferation was determined through the incorporation of 5-bromo-2′-deoxyuridine (BrdU) and measuring the percentage of BrdU-positive cells after 6 h of continuous labeling (10 h for Chondrosia reniformis). Apoptosis was identified using an antibody against active caspase-3. Cell loss through shedding was studied quantitatively by collecting and weighing sponge-expelled detritus and qualitatively by light microscopy of sponge tissue and detritus. All species investigated displayed substantial cell proliferation, predominantly in the choanoderm, but also in the mesohyl. The majority of coral reef species (five) showed between 16.1±15.9% and 19.0±2.0% choanocyte proliferation (mean±SD) after 6 h and the Mediterranean species, C. reniformis, showed 16.6±3.2% after 10 h BrdU-labeling. Monanchora arbuscula showed lower choanocyte proliferation (8.1±3.7%), whereas the mangrove species Mycale microsigmatosa showed relatively higher levels of choanocyte proliferation (70.5±6.6%). Choanocyte proliferation in Haliclona vansoesti was variable (2.8–73.1%). Apoptosis was negligible and not the primary mechanism of cell loss involved in cell turnover. All species investigated produced significant amounts of detritus (2.5–18% detritus bodyweight −1·d −1) and cell shedding was observed in seven out of eight species. The amount of shed cells observed in histological sections may be related to differences in residence time of detritus within canals. Detritus production could not be directly linked to cell shedding due to the degraded nature of expelled cellular debris. We have demonstrated that under steady-state conditions, cell turnover through cell proliferation and cell shedding are common processes to maintain tissue homeostasis in a variety of sponge species from different ecosystems. Cell turnover is hypothesized to be the main underlying mechanism producing sponge-derived detritus, a major trophic resource transferred through sponges in benthic ecosystems, such as coral reefs.

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          Most cited references29

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          Surviving in a marine desert: the sponge loop retains resources within coral reefs.

          Ever since Darwin's early descriptions of coral reefs, scientists have debated how one of the world's most productive and diverse ecosystems can thrive in the marine equivalent of a desert. It is an enigma how the flux of dissolved organic matter (DOM), the largest resource produced on reefs, is transferred to higher trophic levels. Here we show that sponges make DOM available to fauna by rapidly expelling filter cells as detritus that is subsequently consumed by reef fauna. This "sponge loop" was confirmed in aquarium and in situ food web experiments, using (13)C- and (15)N-enriched DOM. The DOM-sponge-fauna pathway explains why biological hot spots such as coral reefs persist in oligotrophic seas--the reef's paradox--and has implications for reef ecosystem functioning and conservation strategies.
            • Record: found
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            Stem cells and their niches.

            A constellation of intrinsic and extrinsic cellular mechanisms regulates the balance of self-renewal and differentiation in all stem cells. Stem cells, their progeny, and elements of their microenvironment make up an anatomical structure that coordinates normal homeostatic production of functional mature cells. Here we discuss the stem cell niche concept, highlight recent progress, and identify important unanswered questions. We focus on three mammalian stem cell systems where large numbers of mature cells must be continuously produced throughout adult life: intestinal epithelium, epidermal structures, and bone marrow.
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              Genomic insights into the marine sponge microbiome.

              Marine sponges (phylum Porifera) often contain dense and diverse microbial communities, which can constitute up to 35% of the sponge biomass. The genome of one sponge, Amphimedon queenslandica, was recently sequenced, and this has provided new insights into the origins of animal evolution. Complementary efforts to sequence the genomes of uncultivated sponge symbionts have yielded the first glimpse of how these intimate partnerships are formed. The remarkable microbial and chemical diversity of the sponge-microorganism association, coupled with its postulated antiquity, makes sponges important model systems for the study of metazoan host-microorganism interactions, and their evolution, as well as for enabling access to biotechnologically important symbiont-derived natural products. In this Review, we discuss our current understanding of the interactions between marine sponges and their microbial symbiotic consortia, and highlight recent insights into these relationships from genomic studies.

                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2014
                7 October 2014
                : 9
                : 10
                : e109486
                Affiliations
                [1 ]Department of Aquatic Ecology and Ecotoxicology, Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, The Netherlands
                [2 ]Porifarma B.V. Poelbos 3, Ede, The Netherlands
                [3 ]Department of Pathology, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands
                [4 ]Department of Molecular Cell Biology, Research Institute Growth and Development, Maastricht University, Maastricht, The Netherlands
                [5 ]Electron Microscopy Unit, CRISP, Maastricht, The Netherlands
                [6 ]Institut de Ciències del Mar-Consejo Superior de Investigaciones Científicas (ICM-CSIC), Barcelona, Spain
                [7 ]Department of Computational Geo-Ecology, Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, The Netherlands
                Australian Institute of Marine Science, Australia
                Author notes

                Competing Interests: BEA, RO, and JMdG are affiliated with Porifarma B.V. Porifarma B.V. received funding from the European Union Seventh Framework Programme (FP7/2007–2013) under grant agreement no KBBE-2010-266033 to undertake the research leading to these results. BEA is employed by Porifarma B.V. under grant agreement no KBBE-2010-266033 from the European Union Seventh Framework Programme (FP7/2007–2013). There are no patents, products in development or marketed products to declare. This does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials.

                Conceived and designed the experiments: BEA RO HGvdG WA JPMC BS JMdG. Performed the experiments: BEA KL MR JMdG. Analyzed the data: EvL BEA FV. Contributed reagents/materials/analysis tools: RO JPMC BS FV MR JMdG. Wrote the paper: BEA RO HGvdG WA JPMC BS MR FV EvL JMdG.

                Article
                PONE-D-14-24731
                10.1371/journal.pone.0109486
                4188633
                25289641
                7fd18017-3e81-4aa1-8ea8-e3e0fbb093e5
                Copyright @ 2014

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 3 June 2014
                : 1 September 2014
                Page count
                Pages: 11
                Funding
                Porifarma B.V. received funding from the European Union Seventh Framework Programme (FP7/2007–2013) under grant agreement no. KBBE-2010–266033 to undertake the research leading to these results. Funding was also received from The Innovational Research Incentives Scheme of the Netherlands Organization for Scientific Research (NWO-VENI; 863.10.009; personal grant to JMdG). Mediterranean sampling was partially funded by the grant CGL2010–18466 from the Spanish Government to MR. BEA, RO, and JMdG are affiliated with Porifarma B.V. Porifarma B.V. provided support in the form of salaries for authors BEA, RO, and JMdG, but no employees of Porifarma B.V. other than BEA, RO, and JMdG had any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the ‘author contributions’ section.
                Categories
                Research Article
                Biology and Life Sciences
                Anatomy
                Histology
                Cell Biology
                Cell Processes
                Cell Cycle and Cell Division
                Cellular Types
                Molecular Cell Biology
                Ecology
                Marine Ecology
                Marine Biology
                Coral Reefs
                Molecular Biology
                Molecular Biology Techniques
                Cell Labeling
                Organisms
                Animals
                Invertebrates
                Sponges
                Physiology
                Physiological Processes
                Homeostasis
                Earth Sciences
                Marine and Aquatic Sciences
                Aquatic Environments
                Marine Environments
                Coasts
                Mangrove Swamps
                Ecology and Environmental Sciences
                Research and analysis methods
                Histochemistry and cytochemistry techniques
                Immunohistochemistry techniques
                Avidin-Biotin immunohistochemistry
                Custom metadata
                The authors confirm that all data underlying the findings are fully available without restriction. All data is within the paper, its supporting information files, and raw data is available through Dryad, doi:10.5061/dryad.q4q52.

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