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Cytoplasmic poly (A)-binding protein critically regulates epidermal maintenance and turnover in the planarian Schmidtea mediterranea
Identifying key cellular events that facilitate stem cell function and tissue organization is crucial for understanding the process of regeneration. Planarians are powerful model system to study regeneration and stem cell (neoblast) function. Here, using planaria, we show that the initial events of...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5611960/ https://www.ncbi.nlm.nih.gov/pubmed/28807897 http://dx.doi.org/10.1242/dev.152942 |
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author | Bansal, Dhiru Kulkarni, Jahnavi Nadahalli, Kavana Lakshmanan, Vairavan Krishna, Srikar Sasidharan, Vidyanand Geo, Jini Dilipkumar, Shilpa Pasricha, Renu Gulyani, Akash Raghavan, Srikala Palakodeti, Dasaradhi |
author_facet | Bansal, Dhiru Kulkarni, Jahnavi Nadahalli, Kavana Lakshmanan, Vairavan Krishna, Srikar Sasidharan, Vidyanand Geo, Jini Dilipkumar, Shilpa Pasricha, Renu Gulyani, Akash Raghavan, Srikala Palakodeti, Dasaradhi |
author_sort | Bansal, Dhiru |
collection | PubMed |
description | Identifying key cellular events that facilitate stem cell function and tissue organization is crucial for understanding the process of regeneration. Planarians are powerful model system to study regeneration and stem cell (neoblast) function. Here, using planaria, we show that the initial events of regeneration, such as epithelialization and epidermal organization are critically regulated by a novel cytoplasmic poly A-binding protein, SMED-PABPC2. Knockdown of smed-pabpc2 leads to defects in epidermal lineage specification, disorganization of epidermis and ECM, and deregulated wound healing, resulting in the selective failure of neoblast proliferation near the wound region. Polysome profiling suggests that epidermal lineage transcripts, including zfp-1, are translationally regulated by SMED-PABPC2. Together, our results uncover a novel role for SMED-PABPC2 in the maintenance of epidermal and ECM integrity, critical for wound healing and subsequent processes for regeneration. |
format | Online Article Text |
id | pubmed-5611960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56119602017-10-06 Cytoplasmic poly (A)-binding protein critically regulates epidermal maintenance and turnover in the planarian Schmidtea mediterranea Bansal, Dhiru Kulkarni, Jahnavi Nadahalli, Kavana Lakshmanan, Vairavan Krishna, Srikar Sasidharan, Vidyanand Geo, Jini Dilipkumar, Shilpa Pasricha, Renu Gulyani, Akash Raghavan, Srikala Palakodeti, Dasaradhi Development Stem Cells and Regeneration Identifying key cellular events that facilitate stem cell function and tissue organization is crucial for understanding the process of regeneration. Planarians are powerful model system to study regeneration and stem cell (neoblast) function. Here, using planaria, we show that the initial events of regeneration, such as epithelialization and epidermal organization are critically regulated by a novel cytoplasmic poly A-binding protein, SMED-PABPC2. Knockdown of smed-pabpc2 leads to defects in epidermal lineage specification, disorganization of epidermis and ECM, and deregulated wound healing, resulting in the selective failure of neoblast proliferation near the wound region. Polysome profiling suggests that epidermal lineage transcripts, including zfp-1, are translationally regulated by SMED-PABPC2. Together, our results uncover a novel role for SMED-PABPC2 in the maintenance of epidermal and ECM integrity, critical for wound healing and subsequent processes for regeneration. The Company of Biologists Ltd 2017-09-01 /pmc/articles/PMC5611960/ /pubmed/28807897 http://dx.doi.org/10.1242/dev.152942 Text en © 2017. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Stem Cells and Regeneration Bansal, Dhiru Kulkarni, Jahnavi Nadahalli, Kavana Lakshmanan, Vairavan Krishna, Srikar Sasidharan, Vidyanand Geo, Jini Dilipkumar, Shilpa Pasricha, Renu Gulyani, Akash Raghavan, Srikala Palakodeti, Dasaradhi Cytoplasmic poly (A)-binding protein critically regulates epidermal maintenance and turnover in the planarian Schmidtea mediterranea |
title | Cytoplasmic poly (A)-binding protein critically regulates epidermal maintenance and turnover in the planarian Schmidtea mediterranea |
title_full | Cytoplasmic poly (A)-binding protein critically regulates epidermal maintenance and turnover in the planarian Schmidtea mediterranea |
title_fullStr | Cytoplasmic poly (A)-binding protein critically regulates epidermal maintenance and turnover in the planarian Schmidtea mediterranea |
title_full_unstemmed | Cytoplasmic poly (A)-binding protein critically regulates epidermal maintenance and turnover in the planarian Schmidtea mediterranea |
title_short | Cytoplasmic poly (A)-binding protein critically regulates epidermal maintenance and turnover in the planarian Schmidtea mediterranea |
title_sort | cytoplasmic poly (a)-binding protein critically regulates epidermal maintenance and turnover in the planarian schmidtea mediterranea |
topic | Stem Cells and Regeneration |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5611960/ https://www.ncbi.nlm.nih.gov/pubmed/28807897 http://dx.doi.org/10.1242/dev.152942 |
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