| Literature DB >> 24834972 |
Miquella G Chavez1, Jimmy Hu2, Kerstin Seidel2, Chunying Li3, Andrew Jheon2, Adrien Naveau4, Orapin Horst5, Ophir D Klein6.
Abstract
Understanding the cellular and molecular mechanisms that underlie tooth regeneration and renewal has become a topic of great interest(1-4), and the mouse incisor provides a model for these processes. This remarkable organ grows continuously throughout the animal's life and generates all the necessary cell types from active pools of adult stem cells housed in the labial (toward the lip) and lingual (toward the tongue) cervical loop (CL) regions. Only the dental stem cells from the labial CL give rise to ameloblasts that generate enamel, the outer covering of teeth, on the labial surface. This asymmetric enamel formation allows abrasion at the incisor tip, and progenitors and stem cells in the proximal incisor ensure that the dental tissues are constantly replenished. The ability to isolate and grow these progenitor or stem cells in vitro allows their expansion and opens doors to numerous experiments not achievable in vivo, such as high throughput testing of potential stem cell regulatory factors. Here, we describe and demonstrate a reliable and consistent method to culture cells from the labial CL of the mouse incisor.Entities:
Mesh:
Year: 2014 PMID: 24834972 PMCID: PMC4141628 DOI: 10.3791/51266
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355