Cargando…

Neoblast Specialization in Regeneration of the Planarian Schmidtea mediterranea

Planarians can regenerate any missing body part in a process requiring dividing cells called neoblasts. Historically, neoblasts have largely been considered a homogeneous stem cell population. Most studies, however, analyzed neoblasts at the population rather than the single-cell level, leaving the...

Descripción completa

Detalles Bibliográficos
Autores principales: Scimone, M. Lucila, Kravarik, Kellie M., Lapan, Sylvain W., Reddien, Peter W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4176530/
https://www.ncbi.nlm.nih.gov/pubmed/25254346
http://dx.doi.org/10.1016/j.stemcr.2014.06.001
_version_ 1782336647624392704
author Scimone, M. Lucila
Kravarik, Kellie M.
Lapan, Sylvain W.
Reddien, Peter W.
author_facet Scimone, M. Lucila
Kravarik, Kellie M.
Lapan, Sylvain W.
Reddien, Peter W.
author_sort Scimone, M. Lucila
collection PubMed
description Planarians can regenerate any missing body part in a process requiring dividing cells called neoblasts. Historically, neoblasts have largely been considered a homogeneous stem cell population. Most studies, however, analyzed neoblasts at the population rather than the single-cell level, leaving the degree of heterogeneity in this population unresolved. We combined RNA sequencing of neoblasts from wounded planarians with expression screening and identified 33 transcription factors transcribed in specific differentiated cells and in small fractions of neoblasts during regeneration. Many neoblast subsets expressing distinct tissue-associated transcription factors were present, suggesting candidate specification into many lineages. Consistent with this possibility, klf, pax3/7, and FoxA were required for the differentiation of cintillo-expressing sensory neurons, dopamine-β-hydroxylase-expressing neurons, and the pharynx, respectively. Together, these results suggest that specification of cell fate for most-to-all regenerative lineages occurs within neoblasts, with regenerative cells of blastemas being generated from a highly heterogeneous collection of lineage-specified neoblasts.
format Online
Article
Text
id pubmed-4176530
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-41765302014-09-30 Neoblast Specialization in Regeneration of the Planarian Schmidtea mediterranea Scimone, M. Lucila Kravarik, Kellie M. Lapan, Sylvain W. Reddien, Peter W. Stem Cell Reports Article Planarians can regenerate any missing body part in a process requiring dividing cells called neoblasts. Historically, neoblasts have largely been considered a homogeneous stem cell population. Most studies, however, analyzed neoblasts at the population rather than the single-cell level, leaving the degree of heterogeneity in this population unresolved. We combined RNA sequencing of neoblasts from wounded planarians with expression screening and identified 33 transcription factors transcribed in specific differentiated cells and in small fractions of neoblasts during regeneration. Many neoblast subsets expressing distinct tissue-associated transcription factors were present, suggesting candidate specification into many lineages. Consistent with this possibility, klf, pax3/7, and FoxA were required for the differentiation of cintillo-expressing sensory neurons, dopamine-β-hydroxylase-expressing neurons, and the pharynx, respectively. Together, these results suggest that specification of cell fate for most-to-all regenerative lineages occurs within neoblasts, with regenerative cells of blastemas being generated from a highly heterogeneous collection of lineage-specified neoblasts. Elsevier 2014-07-04 /pmc/articles/PMC4176530/ /pubmed/25254346 http://dx.doi.org/10.1016/j.stemcr.2014.06.001 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Scimone, M. Lucila
Kravarik, Kellie M.
Lapan, Sylvain W.
Reddien, Peter W.
Neoblast Specialization in Regeneration of the Planarian Schmidtea mediterranea
title Neoblast Specialization in Regeneration of the Planarian Schmidtea mediterranea
title_full Neoblast Specialization in Regeneration of the Planarian Schmidtea mediterranea
title_fullStr Neoblast Specialization in Regeneration of the Planarian Schmidtea mediterranea
title_full_unstemmed Neoblast Specialization in Regeneration of the Planarian Schmidtea mediterranea
title_short Neoblast Specialization in Regeneration of the Planarian Schmidtea mediterranea
title_sort neoblast specialization in regeneration of the planarian schmidtea mediterranea
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4176530/
https://www.ncbi.nlm.nih.gov/pubmed/25254346
http://dx.doi.org/10.1016/j.stemcr.2014.06.001
work_keys_str_mv AT scimonemlucila neoblastspecializationinregenerationoftheplanarianschmidteamediterranea
AT kravarikkelliem neoblastspecializationinregenerationoftheplanarianschmidteamediterranea
AT lapansylvainw neoblastspecializationinregenerationoftheplanarianschmidteamediterranea
AT reddienpeterw neoblastspecializationinregenerationoftheplanarianschmidteamediterranea