Journal
BIOMEDICAL RESEARCH-TOKYO
Volume 38, Issue 1, Pages 61-69Publisher
BIOMEDICAL RESEARCH PRESS LTD
DOI: 10.2220/biomedres.38.61
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Funding
- Japan Society for the Promotion of Science (JSPS) KAKENHI CHOUSENTEKI HOUGA [15K15762]
- Grants-in-Aid for Scientific Research [15K15762, 16H05534, 26670852, 16K20663, 16K15813] Funding Source: KAKEN
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In tooth root development, periodontal ligament (PDL) and cementum are formed by the coordination with the fragmentation of Hertwig's epithelial root sheath (HERS) and the differentiation of dental follicle mesenchymal cells. However, the function of the dental epithelial cells after HERS fragmentation in the PDL is not fully understood. Here, we found that TGF-beta regulated HERS fragmentation via epithelial-mesenchymal transition (EMT), and the fragmented epithelial cells differentiated into PDL fibroblastic cells with expressing of PDL extracellular matrix (ECM). In the histochemical analysis, TGF-beta was expressed in odontoblast layer adjacent of HERS during root development. Periostin expression was detected around fragmented epithelial cells on the root surface, but not in HERS. In the experiment using an established mouse HERS cell line (HERS01a), TGF-beta 1 treatment decreased E-cadherin and relatively increased N-cadherin expression. TGF-beta 1 treatment in HERS01a induced further expression of important ECM proteins for acellular cementum and PDL development such as fibronectin and periostin. Taken together, activation of TGF-beta signaling induces HERS fragmentation through EMT and the fragmented HERS cells contribute to formation of PDL and acellular cementum through periostin and fibronectin expression.
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