4.6 Article

The role of different macrophages-derived conditioned media in dental pulp tissue regeneration

期刊

TISSUE & CELL
卷 79, 期 -, 页码 -

出版社

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.tice.2022.101944

关键词

Pulp regeneration; M1 macrophage; M2 macrophage; Extracellular matrix; Cell sheet

资金

  1. National Natural Science Founda- tion of China
  2. [82060201]

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This study investigated the effects of different phenotype macrophages on dental pulp regeneration. M2 macrophages were found to promote the proliferation, migration, and osteogenic differentiation of hDPSCs, while M1 macrophages led to calcium salt deposition and disorganization of collagen fibers.
Macrophages have been reported to play important roles in tissue repair and regeneration. While it is known that macrophages are present in the dental pulp, their role in dental pulp regeneration is not fully understood. In the present study, we investigated the effects of different phenotype macrophages conditioned medium on the cellular behaviors of hDPSCs and their extracellular matrix (cell sheets) in vitro. Moreover, twenty-four root fragments inserted with cell sheets cultured with different conditioned media were placed into the back subcutaneous space of 6-8-week-old male BALB/c nude mouse. The regenerated tissues in the root fragments were assessed via histologic analysis after 8 weeks of transplantation. M2 macrophages could promote the proliferation, migration, and osteogenic differentiation of hDPSCs. Dental pulp-like tissue with an odontoblast-like layer lining the dentinal surface and well-arranged collagen fibers was harvested in root fragment combined with M2 conditioned medium cultured cell sheet, whereas a large amount of calcium salt deposition and disorganization of collagen fibers were observed in root fragments combined with M1 conditioned medium cultured cell sheet. Therefore, promoting the transformation of M1 into M2 macrophage in dental pulp tissue regeneration may be a potential way for dental pulp regeneration via functional healing.

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