Mechanoresponsive stem cells acquire neural crest fate in jaw regeneration. (22nd November 2018)
- Record Type:
- Journal Article
- Title:
- Mechanoresponsive stem cells acquire neural crest fate in jaw regeneration. (22nd November 2018)
- Main Title:
- Mechanoresponsive stem cells acquire neural crest fate in jaw regeneration
- Authors:
- Ransom, Ryan
Carter, Ava
Salhotra, Ankit
Leavitt, Tripp
Marecic, Owen
Murphy, Matthew
Lopez, Michael
Wei, Yuning
Marshall, Clement
Shen, Ethan
Jones, Ruth
Sharir, Amnon
Klein, Ophir
Chan, Charles
Wan, Derrick
Chang, Howard
Longaker, Michael - Abstract:
- Abstract During both embryonic development and adult tissue regeneration, changes in chromatin structure driven by master transcription factors lead to stimulus-responsive transcriptional programs. A thorough understanding of how stem cells in the skeleton interpret mechanical stimuli and enact regeneration would shed light on how forces are transduced to the nucleus in regenerative processes. Here we develop a genetically dissectible mouse model of mandibular distraction osteogenesis—which is a process that is used in humans to correct an undersized lower jaw that involves surgically separating the jaw bone, which elicits new bone growth in the gap. We use this model to show that regions of newly formed bone are clonally derived from stem cells that reside in the skeleton. Using chromatin and transcriptional profiling, we show that these stem-cell populations gain activity within the focal adhesion kinase (FAK) signalling pathway, and that inhibiting FAK abolishes new bone formation. Mechanotransduction via FAK in skeletal stem cells during distraction activates a gene-regulatory program and retrotransposons that are normally active in primitive neural crest cells, from which skeletal stem cells arise during development. This reversion to a developmental state underlies the robust tissue growth that facilitates stem-cell-based regeneration of adult skeletal tissue. Reversion of adult skeletal stem cells to a developmental state underlies the growth of new bone during jawAbstract During both embryonic development and adult tissue regeneration, changes in chromatin structure driven by master transcription factors lead to stimulus-responsive transcriptional programs. A thorough understanding of how stem cells in the skeleton interpret mechanical stimuli and enact regeneration would shed light on how forces are transduced to the nucleus in regenerative processes. Here we develop a genetically dissectible mouse model of mandibular distraction osteogenesis—which is a process that is used in humans to correct an undersized lower jaw that involves surgically separating the jaw bone, which elicits new bone growth in the gap. We use this model to show that regions of newly formed bone are clonally derived from stem cells that reside in the skeleton. Using chromatin and transcriptional profiling, we show that these stem-cell populations gain activity within the focal adhesion kinase (FAK) signalling pathway, and that inhibiting FAK abolishes new bone formation. Mechanotransduction via FAK in skeletal stem cells during distraction activates a gene-regulatory program and retrotransposons that are normally active in primitive neural crest cells, from which skeletal stem cells arise during development. This reversion to a developmental state underlies the robust tissue growth that facilitates stem-cell-based regeneration of adult skeletal tissue. Reversion of adult skeletal stem cells to a developmental state underlies the growth of new bone during jaw regeneration, in a process that relies on mechanotransduction via the focal adhesion kinase protein. … (more)
- Is Part Of:
- Nature. Volume 563:Number 7732(2018)
- Journal:
- Nature
- Issue:
- Volume 563:Number 7732(2018)
- Issue Display:
- Volume 563, Issue 7732 (2018)
- Year:
- 2018
- Volume:
- 563
- Issue:
- 7732
- Issue Sort Value:
- 2018-0563-7732-0000
- Page Start:
- 514
- Page End:
- 521
- Publication Date:
- 2018-11-22
- Subjects:
- Science -- Periodicals
505 - Journal URLs:
- http://www.nature.com/nature/ ↗
http://www.nature.com/ ↗ - DOI:
- 10.1038/s41586-018-0650-9 ↗
- Languages:
- English
- ISSNs:
- 0028-0836
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6045.000000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11147.xml