Correlation Engine 2.0
Clear Search sequence regions


  • 1 receptor (2)
  • alizarin red (1)
  • behavior (1)
  • CD206 (2)
  • CD80 (1)
  • cellular (2)
  • collagen (1)
  • cytokines (1)
  • dental papilla (1)
  • DSPP (1)
  • factors (1)
  • growth factor (1)
  • humans (1)
  • IL 10 (2)
  • IL 1RA (2)
  • IL 1β (2)
  • IL 6 (1)
  • IL 8 (1)
  • interleukin (2)
  • interleukin 1 (2)
  • interleukin 10 (2)
  • interleukin 4 (2)
  • macrophage (9)
  • MCP 1 (1)
  • MIP 1β (2)
  • molds (1)
  • organoid (3)
  • phase (1)
  • stem cell (5)
  • tgf β1 (2)
  • TNF (4)
  • tooth (1)
  • tumor necrosis factor α (3)
  • Sizes of these terms reflect their relevance to your search.

    Immune cell-mesenchymal stem cell crosstalk modulates the process of repair and regeneration. In this study, a novel heterogeneous cell containing a matrix-based 3-dimensional (3D) tissue construct was used to study the interactions between stem cells from apical papilla (SCAPs) and macrophage for a comprehensive understanding on the cellular signaling mechanisms guiding inflammation and repair. SCAPs and macrophages were seeded with collagen in 3D-printed molds to generate self-assembled tissue constructs, which were exposed to 3 conditions: no stimulation, lipopolysaccharide (LPS), and interleukin (IL)-4 from 0 to 14 days. Specimens from each group were evaluated for cellular interactions, inflammatory mediators (IL-1β, tumor necrosis factor [TNF]-α, macrophage-derived chemokine [MDC], macrophage inflammatory protein [MIP]-1β, monocyte chemoattractant protein [MCP]-1, IL-6, IL-8, transforming growth factor [TGF]-β1, IL-1RA, IL-10), expression of surface markers (CD80, 206), transcription factors (pSTAT1, pSTAT6), and SCAP differentiation markers (dentin sialophosphoprotein [DSPP], dentin matrix acidic phosphoprotein 1 [DMP-1], and alizarin red) using confocal laser scanning microscopy and multiplex cytokine profiling from 2 to 14 days. SCAP and macrophages displayed a cytokine-mediated interaction and differentiation characteristics. The increased pro-inflammatory cytokines/chemokines, IL-1β, TNF-α, MDC, and MIP-1β, in the earlier phase followed by the higher ratio of pSTAT6/pSTAT1 and decreased CD206 (P < .05), indicated a distinct polarization behavior in macrophages during repair in the LPS group. Conversely, the equal ratio of pSTAT6/pSTAT1, late increase in CD206, and amplified secretion of IL-1RA, IL-10, and TGF-β1 (P < .05) in the anti-inflammatory environment, directed alternative macrophage polarization, promoting SCAP differentiation and tissue modeling in IL-4 group. The novel 3D organoid system developed in this study allowed a comprehensive analysis of the SCAP-macrophage interactions during inflammation and healing, providing a deeper insight on the periapical dynamics of the immature tooth. Copyright © 2022 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.

    Citation

    Fang-Chi Li, Hebatullah Hussein, Marco Magalhaes, P Ravi Selvaganapathy, Anil Kishen. Deciphering Stem Cell From Apical Papilla-Macrophage Choreography Using a Novel 3-dimensional Organoid System. Journal of endodontics. 2022 Aug;48(8):1063-1072.e7

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 35513088

    View Full Text