Cargando…

Transcriptional Analysis of Fracture Healing and the Induction of Embryonic Stem Cell–Related Genes

Fractures are among the most common human traumas. Fracture healing represents a unique temporarily definable post-natal process in which to study the complex interactions of multiple molecular events that regulate endochondral skeletal tissue formation. Because of the regenerative nature of fractur...

Descripción completa

Detalles Bibliográficos
Autores principales: Bais, Manish, McLean, Jody, Sebastiani, Paola, Young, Megan, Wigner, Nathan, Smith, Temple, Kotton, Darrell N., Einhorn, Thomas A., Gerstenfeld, Louis C.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2673045/
https://www.ncbi.nlm.nih.gov/pubmed/19415118
http://dx.doi.org/10.1371/journal.pone.0005393
_version_ 1782166570490920960
author Bais, Manish
McLean, Jody
Sebastiani, Paola
Young, Megan
Wigner, Nathan
Smith, Temple
Kotton, Darrell N.
Einhorn, Thomas A.
Gerstenfeld, Louis C.
author_facet Bais, Manish
McLean, Jody
Sebastiani, Paola
Young, Megan
Wigner, Nathan
Smith, Temple
Kotton, Darrell N.
Einhorn, Thomas A.
Gerstenfeld, Louis C.
author_sort Bais, Manish
collection PubMed
description Fractures are among the most common human traumas. Fracture healing represents a unique temporarily definable post-natal process in which to study the complex interactions of multiple molecular events that regulate endochondral skeletal tissue formation. Because of the regenerative nature of fracture healing, it is hypothesized that large numbers of post-natal stem cells are recruited and contribute to formation of the multiple cell lineages that contribute to this process. Bayesian modeling was used to generate the temporal profiles of the transcriptome during fracture healing. The temporal relationships between ontologies that are associated with various biologic, metabolic, and regulatory pathways were identified and related to developmental processes associated with skeletogenesis, vasculogenesis, and neurogenesis. The complement of all the expressed BMPs, Wnts, FGFs, and their receptors were related to the subsets of transcription factors that were concurrently expressed during fracture healing. We further defined during fracture healing the temporal patterns of expression for 174 of the 193 genes known to be associated with human genetic skeletal disorders. In order to identify the common regulatory features that might be present in stem cells that are recruited during fracture healing to other types of stem cells, we queried the transcriptome of fracture healing against that seen in embryonic stem cells (ESCs) and mesenchymal stem cells (MSCs). Approximately 300 known genes that are preferentially expressed in ESCs and ∼350 of the known genes that are preferentially expressed in MSCs showed induction during fracture healing. Nanog, one of the central epigenetic regulators associated with ESC stem cell maintenance, was shown to be associated in multiple forms or bone repair as well as MSC differentiation. In summary, these data present the first temporal analysis of the transcriptome of an endochondral bone formation process that takes place during fracture healing. They show that neurogenesis as well as vasculogenesis are predominant components of skeletal tissue formation and suggest common pathways are shared between post-natal stem cells and those seen in ESCs.
format Text
id pubmed-2673045
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-26730452009-05-05 Transcriptional Analysis of Fracture Healing and the Induction of Embryonic Stem Cell–Related Genes Bais, Manish McLean, Jody Sebastiani, Paola Young, Megan Wigner, Nathan Smith, Temple Kotton, Darrell N. Einhorn, Thomas A. Gerstenfeld, Louis C. PLoS One Research Article Fractures are among the most common human traumas. Fracture healing represents a unique temporarily definable post-natal process in which to study the complex interactions of multiple molecular events that regulate endochondral skeletal tissue formation. Because of the regenerative nature of fracture healing, it is hypothesized that large numbers of post-natal stem cells are recruited and contribute to formation of the multiple cell lineages that contribute to this process. Bayesian modeling was used to generate the temporal profiles of the transcriptome during fracture healing. The temporal relationships between ontologies that are associated with various biologic, metabolic, and regulatory pathways were identified and related to developmental processes associated with skeletogenesis, vasculogenesis, and neurogenesis. The complement of all the expressed BMPs, Wnts, FGFs, and their receptors were related to the subsets of transcription factors that were concurrently expressed during fracture healing. We further defined during fracture healing the temporal patterns of expression for 174 of the 193 genes known to be associated with human genetic skeletal disorders. In order to identify the common regulatory features that might be present in stem cells that are recruited during fracture healing to other types of stem cells, we queried the transcriptome of fracture healing against that seen in embryonic stem cells (ESCs) and mesenchymal stem cells (MSCs). Approximately 300 known genes that are preferentially expressed in ESCs and ∼350 of the known genes that are preferentially expressed in MSCs showed induction during fracture healing. Nanog, one of the central epigenetic regulators associated with ESC stem cell maintenance, was shown to be associated in multiple forms or bone repair as well as MSC differentiation. In summary, these data present the first temporal analysis of the transcriptome of an endochondral bone formation process that takes place during fracture healing. They show that neurogenesis as well as vasculogenesis are predominant components of skeletal tissue formation and suggest common pathways are shared between post-natal stem cells and those seen in ESCs. Public Library of Science 2009-05-05 /pmc/articles/PMC2673045/ /pubmed/19415118 http://dx.doi.org/10.1371/journal.pone.0005393 Text en Bais 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
Bais, Manish
McLean, Jody
Sebastiani, Paola
Young, Megan
Wigner, Nathan
Smith, Temple
Kotton, Darrell N.
Einhorn, Thomas A.
Gerstenfeld, Louis C.
Transcriptional Analysis of Fracture Healing and the Induction of Embryonic Stem Cell–Related Genes
title Transcriptional Analysis of Fracture Healing and the Induction of Embryonic Stem Cell–Related Genes
title_full Transcriptional Analysis of Fracture Healing and the Induction of Embryonic Stem Cell–Related Genes
title_fullStr Transcriptional Analysis of Fracture Healing and the Induction of Embryonic Stem Cell–Related Genes
title_full_unstemmed Transcriptional Analysis of Fracture Healing and the Induction of Embryonic Stem Cell–Related Genes
title_short Transcriptional Analysis of Fracture Healing and the Induction of Embryonic Stem Cell–Related Genes
title_sort transcriptional analysis of fracture healing and the induction of embryonic stem cell–related genes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2673045/
https://www.ncbi.nlm.nih.gov/pubmed/19415118
http://dx.doi.org/10.1371/journal.pone.0005393
work_keys_str_mv AT baismanish transcriptionalanalysisoffracturehealingandtheinductionofembryonicstemcellrelatedgenes
AT mcleanjody transcriptionalanalysisoffracturehealingandtheinductionofembryonicstemcellrelatedgenes
AT sebastianipaola transcriptionalanalysisoffracturehealingandtheinductionofembryonicstemcellrelatedgenes
AT youngmegan transcriptionalanalysisoffracturehealingandtheinductionofembryonicstemcellrelatedgenes
AT wignernathan transcriptionalanalysisoffracturehealingandtheinductionofembryonicstemcellrelatedgenes
AT smithtemple transcriptionalanalysisoffracturehealingandtheinductionofembryonicstemcellrelatedgenes
AT kottondarrelln transcriptionalanalysisoffracturehealingandtheinductionofembryonicstemcellrelatedgenes
AT einhornthomasa transcriptionalanalysisoffracturehealingandtheinductionofembryonicstemcellrelatedgenes
AT gerstenfeldlouisc transcriptionalanalysisoffracturehealingandtheinductionofembryonicstemcellrelatedgenes