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. 2018 Jan 25;9:378. doi: 10.1038/s41467-017-02785-6

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 2 — Lineage tracing of CD90/Thy1 in the postnatal mouse incisor. CD90/Thy1 cre mouse line crossed with different reporter lines, a Rosa26R;-mTmG, b Rosa26R-tdTomato, c Rosa26R;-LacZ, and d Rosa26R;-Confetti, shows CD90/Thy1 expressing cells and their progeny contribute to pulp cells and odontoblasts. d Confetti predominately labels single cell clones; thus each single color represents the progeny from one stem cell. e Enlarged region from each reporter line showing CD90/Thy1-derived odontoblasts. PN5-10 postnatal incisor samples were used in a–c, PN21 mouse incisors were used in d. N > = 5 pups each group