Academic Journal

Organoids from mouse molar and incisor as new tools to study tooth-specific biology and development

التفاصيل البيبلوغرافية
العنوان: Organoids from mouse molar and incisor as new tools to study tooth-specific biology and development
المؤلفون: HERMANS, Florian, HEMERYCK, Lara, Bueds, Celine, Torres Pereiro, Marc, HASEVOETS, Steffie, Kobayashi, Hiroto, Lambrechts, Diether, LAMBRICHTS, Ivo, BRONCKAERS, Annelies, Vankelecom, Hugo
المساهمون: HERMANS, Florian, HEMERYCK, Lara, Bueds, Celine, Torres Pereiro, Marc, HASEVOETS, Steffie, Kobayashi, Hiroto, Lambrechts, Diether, LAMBRICHTS, Ivo, BRONCKAERS, Annelies, Vankelecom, Hugo
بيانات النشر: Cell Press
سنة النشر: 2023
المجموعة: Document Server@UHasselt (Universiteit Hasselt)
مصطلحات موضوعية: ameloblasts, assembloids, dental epithelium, incisors, molars, organoids, single-cell RNA-sequencing, stem cells, tooth development, Animals, Mice, Humans, Molar, Cell Differentiation, Biology, Incisor
الوصف: Organoid models provide powerful tools to study tissue biology and development in a dish. Presently, organoids have not yet been developed from mouse tooth. Here, we established tooth organoids (TOs) from early-postnatal mouse molar and incisor, which are long-term expandable, express dental epithelium stem cell (DESC) markers, and recapitulate key properties of the dental epithelium in a tooth-type-specific manner. TOs display in vitro differentiation capacity toward ameloblast-resembling cells, even more pronounced in assembloids in which dental mesenchymal (pulp) stem cells are combined with the organoid DESCs. Single-cell transcriptomics supports this developmental potential and reveals co-differentiation into junctional epithelium- and odontoblast-/cementoblast-like cells in the assembloids. Finally, TOs survive and show ameloblast-resembling differentiation also in vivo. The developed organoid models provide new tools to study mouse tooth-type-specific biology and development and gain deeper molecular and functional insights that may eventually help to achieve future human biological tooth repair and replacement. ; We are grateful to Evelyne Van Kerckhove (UHasselt), Marc Jans (UHasselt), Jeanine Santermans (UHasselt), and Veerle Vanslembrouck (KU Leuven) for valuable technical help. We thank Dr. Diether Lambrechts’ group (VIB,KULeuven) for technical assistance in 103 Genomics. Computational resources for transcriptome analyses were provided by the ‘‘Vlaams Supercomputer Centrum’’ (VSC), managed by the Fund for Scientific Research (FWO), Flanders (Belgium).We are also grateful to the ImagingCore (VIB,KULeuven) and the CIC (KU Leuven) for use ofmicroscopes and the Center for Brain & Disease Research (CBD) Histology unit (VIB, KU Leuven) for use of histology equipment. We acknowledge the use of the TEMplatforms at VIB-KU Leuven, UHasselt, and Tohoku University. The authors also thank Dr. Adrian Ranga (KU Leuven), Dr. Ronald Driesen(UHasselt), and other non-coauthor members of the Laboratory of Tissue ...
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
تدمد: 2213-6711
Relation: Stem Cell Reports, 18 (5) , p. 1166 -1181; http://hdl.handle.net/1942/40106; 1181; 1166; 18; 001017408400001; https://www.cell.com/stem-cell-reports/fulltext/S2213-6711(23)00099-1
DOI: 10.1016/j.stemcr.2023.03.011
الاتاحة: http://hdl.handle.net/1942/40106
https://doi.org/10.1016/j.stemcr.2023.03.011
https://www.cell.com/stem-cell-reports/fulltext/S2213-6711(23)00099-1
رقم الانضمام: edsbas.1CD5A30B
قاعدة البيانات: BASE
الوصف
تدمد:22136711
DOI:10.1016/j.stemcr.2023.03.011