Protein S100-A7 derived from digested dentin is a critical molecule for dentin pulp regeneration

Shungo Komichi, Yusuke Takahashi, Motoki Okamoto, Manahil Ali, Masakatsu Watanabe, Hailing Huang, Takeo Nakai, Paul Cooper, Mikako Hayashi

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)
128 Downloads (Pure)


Dentin consists of inorganic hard tissue and organic dentin matrix components (DMCs). Various kinds of bioactive molecules are included in DMCs and some of them can be released after digestion by endogenous matrix metalloproteinases (MMPs) in the caries region. Digested DMCs induced by MMP20 have been reported to promote pulpal wound healing processes, but the released critical molecules responsible for this phenomenon are unclear. Here, we identified protein S100-A7 as a critical molecule for pulpal healing in digested DMCs by comprehensive proteomic approaches and following pulp capping experiments in rat molars. In addition, immunohistochemical results indicated the specific distribution of S100-A7 and receptor for advanced glycation end-products (RAGE) as receptor for S100-A7 in the early stage of the pulpal healing process, and following accumulation of CD146-positive stem cells in wounded pulp. Our findings indicate that protein S100-A7 released from dentin by MMP20 might play a key role in dentin pulp regeneration.
Original languageEnglish
Article number1002
Issue number9
Publication statusPublished - 29 Aug 2019


  • wound healing
  • pulp capping materials
  • dentinogenesis
  • proteomics


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