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...

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Main Authors: Yoshihiro Sowa, Tetsuya Imura, Toshiaki Numajiri, Kosuke Takeda, Yo Mabuchi, Yumi Matsuzaki, Kenichi Nishino
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24391913/pdf/?tool=EBI
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spelling doaj-0e7cc83d44514f69a61798326f8d62ec2021-06-19T05:01:38ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01812e8420610.1371/journal.pone.0084206Adipose stromal cells contain phenotypically distinct adipogenic progenitors derived from neural crest.Yoshihiro SowaTetsuya ImuraToshiaki NumajiriKosuke TakedaYo MabuchiYumi MatsuzakiKenichi NishinoRecent 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.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24391913/pdf/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Yoshihiro Sowa
Tetsuya Imura
Toshiaki Numajiri
Kosuke Takeda
Yo Mabuchi
Yumi Matsuzaki
Kenichi Nishino
spellingShingle 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.
PLoS ONE
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)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
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.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24391913/pdf/?tool=EBI
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