A quiescent cell population replenishes mesenchymal stem cells to drive accelerated growth in mouse incisors
Zhengwen An,
Maja Sabalic,
Ryan F. Bloomquist,
Teresa E. Fowler,
Todd Streelman and
Paul T Sharpe ()
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Zhengwen An: Kings College London
Maja Sabalic: Kings College London
Ryan F. Bloomquist: Georgia Institute of Technology
Teresa E. Fowler: Georgia Institute of Technology
Todd Streelman: Georgia Institute of Technology
Paul T Sharpe: Kings College London
Nature Communications, 2018, vol. 9, issue 1, 1-9
Abstract:
Abstract The extent to which heterogeneity within mesenchymal stem cell (MSC) populations is related to function is not understood. Using the archetypal MSC in vitro surface marker, CD90/Thy1, here we show that 30% of the MSCs in the continuously growing mouse incisor express CD90/Thy1 and these cells give rise to 30% of the differentiated cell progeny during postnatal development. In adulthood, when growth rate homeostasis is established, the CD90/Thy1+ MSCs decrease dramatically in number. When adult incisors are cut, the growth rate increases to rapidly re-establish tooth length and homeostasis. This accelerated growth rate correlates with the re-appearance of CD90/Thy+ MSCs and re-establishment of their contribution to cell differentiation. A population of Celsr1+ quiescent cells becomes mitotic following clipping and replenishes the CD90/Thy1 population. A sub-population of MSCs thus exists in the mouse incisor, distinguished by expression of CD90/Thy1 that plays a specific role only during periods of increased growth rate.
Date: 2018
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-017-02785-6
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DOI: 10.1038/s41467-017-02785-6
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