論文

査読有り 国際誌
2018年11月

Detection of bone marrow-derived fibrocytes in human dental pulp repair.

International endodontic journal
  • N Yoshiba
  • ,
  • N Edanami
  • ,
  • A Tohma
  • ,
  • R Takeuchi
  • ,
  • N Ohkura
  • ,
  • A Hosoya
  • ,
  • Y Noiri
  • ,
  • H Nakamura
  • ,
  • K Yoshiba

51
11
開始ページ
1187
終了ページ
1195
記述言語
英語
掲載種別
DOI
10.1111/iej.12940

AIM: To explore the expression profile of CD45+/pro-collagen I+ fibrocytes in intact dental pulps as well as during wound healing in adult dental pulp tissue. METHODOLOGY: A total of 16 healthy permanent teeth were obtained from young patients (18 to 25 years) undergoing orthodontic treatment. Routine pulp capping with mineral trioxide aggregate (MTA) was performed under local anaesthesia to induce a mineralized barrier at the exposed surface. Teeth were extracted from patients after 7, 14 and 35 days. Sections of the extracted teeth were prepared and stained for various markers using indirect immunofluorescence. Fibrocytes were counted, and the data were statistically evaluated using the Dunnett test. RESULTS: In uninflammed pulp tissue, a pro-collagen I-positive reaction was detected in odontoblasts, as well as in perivascular cells. Most of the CD45-positive cells were negative for pro-collagen I in normal pulp tissue, whereas CD45+/pro-collagen I+ fibrocytes were detected 7 days after injury. At day 14, fibrocytes were recognized under the fibrous matrix in contact with MTA and had infiltrated into regions of new capillary formation, where the fibrocytes were positively stained for vascular endothelial growth factor. By 35 days, fibrocytes were few, coincident with the formation of dentine bridges. The number of fibrocytes peaked 7 days post-injury and decreased at 14 days. CONCLUSIONS: The presence of fibrocytes in human pulp wound healing was observed. The spatiotemporal distribution of fibrocytes suggests that fibrocytes are involved in the early stages of pulp wound healing, specifically by contributing to new blood vessel formation.

リンク情報
DOI
https://doi.org/10.1111/iej.12940
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/29679496
ID情報
  • DOI : 10.1111/iej.12940
  • ISSN : 0143-2885
  • PubMed ID : 29679496

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