Adipose stromal cells contain phenotypically distinct adipogenic progenitors derived from neural crest.

Recent studies have shown that adipose-derived stromal/stem cells (ASCs) contain phenotypically and functionally heterogeneous subpopulations of cells, but their developmental origin and their relative differentiation potential remain elusive. In the present study, we aimed at investigating how and...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Yoshihiro Sowa, Tetsuya Imura, Toshiaki Numajiri, Kosuke Takeda, Yo Mabuchi, Yumi Matsuzaki, Kenichi Nishino
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2013
Materias:
R
Q
Acceso en línea:https://doaj.org/article/0e7cc83d44514f69a61798326f8d62ec
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:0e7cc83d44514f69a61798326f8d62ec
record_format dspace
spelling oai:doaj.org-article:0e7cc83d44514f69a61798326f8d62ec2021-11-18T08:39:23ZAdipose stromal cells contain phenotypically distinct adipogenic progenitors derived from neural crest.1932-620310.1371/journal.pone.0084206https://doaj.org/article/0e7cc83d44514f69a61798326f8d62ec2013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24391913/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Recent studies have shown that adipose-derived stromal/stem cells (ASCs) contain phenotypically and functionally heterogeneous subpopulations of cells, but their developmental origin and their relative differentiation potential remain elusive. In the present study, we aimed at investigating how and to what extent the neural crest contributes to ASCs using Cre-loxP-mediated fate mapping. ASCs harvested from subcutaneous fat depots of either adult P0-Cre/or Wnt1-Cre/Floxed-reporter mice contained a few neural crest-derived ASCs (NCDASCs). This subpopulation of cells was successfully expanded in vitro under standard culture conditions and their growth rate was comparable to non-neural crest derivatives. Although NCDASCs were positive for several mesenchymal stem cell markers as non-neural crest derivatives, they exhibited a unique bipolar or multipolar morphology with higher expression of markers for both neural crest progenitors (p75NTR, Nestin, and Sox2) and preadipocytes (CD24, CD34, S100, Pref-1, GATA2, and C/EBP-delta). NCDASCs were able to differentiate into adipocytes with high efficiency but their osteogenic and chondrogenic potential was markedly attenuated, indicating their commitment to adipogenesis. In vivo, a very small proportion of adipocytes were originated from the neural crest. In addition, p75NTR-positive neural crest-derived cells were identified along the vessels within the subcutaneous adipose tissue, but they were negative for mural and endothelial markers. These results demonstrate that ASCs contain neural crest-derived adipocyte-restricted progenitors whose phenotype is distinct from that of non-neural crest derivatives.Yoshihiro SowaTetsuya ImuraToshiaki NumajiriKosuke TakedaYo MabuchiYumi MatsuzakiKenichi NishinoPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 12, p e84206 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Yoshihiro Sowa
Tetsuya Imura
Toshiaki Numajiri
Kosuke Takeda
Yo Mabuchi
Yumi Matsuzaki
Kenichi Nishino
Adipose stromal cells contain phenotypically distinct adipogenic progenitors derived from neural crest.
description Recent studies have shown that adipose-derived stromal/stem cells (ASCs) contain phenotypically and functionally heterogeneous subpopulations of cells, but their developmental origin and their relative differentiation potential remain elusive. In the present study, we aimed at investigating how and to what extent the neural crest contributes to ASCs using Cre-loxP-mediated fate mapping. ASCs harvested from subcutaneous fat depots of either adult P0-Cre/or Wnt1-Cre/Floxed-reporter mice contained a few neural crest-derived ASCs (NCDASCs). This subpopulation of cells was successfully expanded in vitro under standard culture conditions and their growth rate was comparable to non-neural crest derivatives. Although NCDASCs were positive for several mesenchymal stem cell markers as non-neural crest derivatives, they exhibited a unique bipolar or multipolar morphology with higher expression of markers for both neural crest progenitors (p75NTR, Nestin, and Sox2) and preadipocytes (CD24, CD34, S100, Pref-1, GATA2, and C/EBP-delta). NCDASCs were able to differentiate into adipocytes with high efficiency but their osteogenic and chondrogenic potential was markedly attenuated, indicating their commitment to adipogenesis. In vivo, a very small proportion of adipocytes were originated from the neural crest. In addition, p75NTR-positive neural crest-derived cells were identified along the vessels within the subcutaneous adipose tissue, but they were negative for mural and endothelial markers. These results demonstrate that ASCs contain neural crest-derived adipocyte-restricted progenitors whose phenotype is distinct from that of non-neural crest derivatives.
format article
author Yoshihiro Sowa
Tetsuya Imura
Toshiaki Numajiri
Kosuke Takeda
Yo Mabuchi
Yumi Matsuzaki
Kenichi Nishino
author_facet Yoshihiro Sowa
Tetsuya Imura
Toshiaki Numajiri
Kosuke Takeda
Yo Mabuchi
Yumi Matsuzaki
Kenichi Nishino
author_sort Yoshihiro Sowa
title Adipose stromal cells contain phenotypically distinct adipogenic progenitors derived from neural crest.
title_short Adipose stromal cells contain phenotypically distinct adipogenic progenitors derived from neural crest.
title_full Adipose stromal cells contain phenotypically distinct adipogenic progenitors derived from neural crest.
title_fullStr Adipose stromal cells contain phenotypically distinct adipogenic progenitors derived from neural crest.
title_full_unstemmed Adipose stromal cells contain phenotypically distinct adipogenic progenitors derived from neural crest.
title_sort adipose stromal cells contain phenotypically distinct adipogenic progenitors derived from neural crest.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/0e7cc83d44514f69a61798326f8d62ec
work_keys_str_mv AT yoshihirosowa adiposestromalcellscontainphenotypicallydistinctadipogenicprogenitorsderivedfromneuralcrest
AT tetsuyaimura adiposestromalcellscontainphenotypicallydistinctadipogenicprogenitorsderivedfromneuralcrest
AT toshiakinumajiri adiposestromalcellscontainphenotypicallydistinctadipogenicprogenitorsderivedfromneuralcrest
AT kosuketakeda adiposestromalcellscontainphenotypicallydistinctadipogenicprogenitorsderivedfromneuralcrest
AT yomabuchi adiposestromalcellscontainphenotypicallydistinctadipogenicprogenitorsderivedfromneuralcrest
AT yumimatsuzaki adiposestromalcellscontainphenotypicallydistinctadipogenicprogenitorsderivedfromneuralcrest
AT kenichinishino adiposestromalcellscontainphenotypicallydistinctadipogenicprogenitorsderivedfromneuralcrest
_version_ 1718421483528650752