Cargando…
Osx-Cre Targets Multiple Cell Types besides Osteoblast Lineage in Postnatal Mice
Osterix (Osx or Sp7) is a zinc-finger-family transcriptional factor essential for osteoblast differentiation in mammals. The Osx-Cre mouse line (also known as Osx1-GFP::Cre) expresses GFP::Cre fusion protein from a BAC transgene containing the Osx regulatory sequence. The mouse strain was initially...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893188/ https://www.ncbi.nlm.nih.gov/pubmed/24454809 http://dx.doi.org/10.1371/journal.pone.0085161 |
_version_ | 1782299637904834560 |
---|---|
author | Chen, Jianquan Shi, Yu Regan, Jenna Karuppaiah, Kannan Ornitz, David M. Long, Fanxin |
author_facet | Chen, Jianquan Shi, Yu Regan, Jenna Karuppaiah, Kannan Ornitz, David M. Long, Fanxin |
author_sort | Chen, Jianquan |
collection | PubMed |
description | Osterix (Osx or Sp7) is a zinc-finger-family transcriptional factor essential for osteoblast differentiation in mammals. The Osx-Cre mouse line (also known as Osx1-GFP::Cre) expresses GFP::Cre fusion protein from a BAC transgene containing the Osx regulatory sequence. The mouse strain was initially characterized during embryogenesis, and found to target mainly osteoblast-lineage cells. Because the strain has been increasingly used in postnatal studies, it is important to evaluate its targeting specificity in mice after birth. By crossing the Osx-Cre mouse with the R26-mT/mG reporter line and analyzing the progenies at two months of age, we find that Osx-Cre targets not only osteoblasts, osteocytes and hypertrophic chondrocytes as expected, but also stromal cells, adipocytes and perivascular cells in the bone marrow. The targeting of adipocytes and perivascular cells appears to be specific to those residing within the bone marrow, as the same cell types elsewhere are not targeted. Beyond the skeleton, Osx-Cre also targets the olfactory glomerular cells, and a subset of the gastric and intestinal epithelium. Thus, potential contributions from the non-osteoblast-lineage cells should be considered when Osx-Cre is used to study gene functions in postnatal mice. |
format | Online Article Text |
id | pubmed-3893188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38931882014-01-21 Osx-Cre Targets Multiple Cell Types besides Osteoblast Lineage in Postnatal Mice Chen, Jianquan Shi, Yu Regan, Jenna Karuppaiah, Kannan Ornitz, David M. Long, Fanxin PLoS One Research Article Osterix (Osx or Sp7) is a zinc-finger-family transcriptional factor essential for osteoblast differentiation in mammals. The Osx-Cre mouse line (also known as Osx1-GFP::Cre) expresses GFP::Cre fusion protein from a BAC transgene containing the Osx regulatory sequence. The mouse strain was initially characterized during embryogenesis, and found to target mainly osteoblast-lineage cells. Because the strain has been increasingly used in postnatal studies, it is important to evaluate its targeting specificity in mice after birth. By crossing the Osx-Cre mouse with the R26-mT/mG reporter line and analyzing the progenies at two months of age, we find that Osx-Cre targets not only osteoblasts, osteocytes and hypertrophic chondrocytes as expected, but also stromal cells, adipocytes and perivascular cells in the bone marrow. The targeting of adipocytes and perivascular cells appears to be specific to those residing within the bone marrow, as the same cell types elsewhere are not targeted. Beyond the skeleton, Osx-Cre also targets the olfactory glomerular cells, and a subset of the gastric and intestinal epithelium. Thus, potential contributions from the non-osteoblast-lineage cells should be considered when Osx-Cre is used to study gene functions in postnatal mice. Public Library of Science 2014-01-15 /pmc/articles/PMC3893188/ /pubmed/24454809 http://dx.doi.org/10.1371/journal.pone.0085161 Text en © 2014 Chen et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited. |
spellingShingle | Research Article Chen, Jianquan Shi, Yu Regan, Jenna Karuppaiah, Kannan Ornitz, David M. Long, Fanxin Osx-Cre Targets Multiple Cell Types besides Osteoblast Lineage in Postnatal Mice |
title |
Osx-Cre Targets Multiple Cell Types besides Osteoblast Lineage in Postnatal Mice |
title_full |
Osx-Cre Targets Multiple Cell Types besides Osteoblast Lineage in Postnatal Mice |
title_fullStr |
Osx-Cre Targets Multiple Cell Types besides Osteoblast Lineage in Postnatal Mice |
title_full_unstemmed |
Osx-Cre Targets Multiple Cell Types besides Osteoblast Lineage in Postnatal Mice |
title_short |
Osx-Cre Targets Multiple Cell Types besides Osteoblast Lineage in Postnatal Mice |
title_sort | osx-cre targets multiple cell types besides osteoblast lineage in postnatal mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893188/ https://www.ncbi.nlm.nih.gov/pubmed/24454809 http://dx.doi.org/10.1371/journal.pone.0085161 |
work_keys_str_mv | AT chenjianquan osxcretargetsmultiplecelltypesbesidesosteoblastlineageinpostnatalmice AT shiyu osxcretargetsmultiplecelltypesbesidesosteoblastlineageinpostnatalmice AT reganjenna osxcretargetsmultiplecelltypesbesidesosteoblastlineageinpostnatalmice AT karuppaiahkannan osxcretargetsmultiplecelltypesbesidesosteoblastlineageinpostnatalmice AT ornitzdavidm osxcretargetsmultiplecelltypesbesidesosteoblastlineageinpostnatalmice AT longfanxin osxcretargetsmultiplecelltypesbesidesosteoblastlineageinpostnatalmice |