Role of Resolvin E1 in macrophage polarization as a therapeutic strategy for root resorption: In silico and in vitro analysis

Objectives: This study aimed to evaluate the interaction of Resolvin E1 with macrophage-associated inflammatory markers and assess its potential role in macrophage polarization relevant to root resorption therapy. Methods: Molecular docking was performed using AutoDock Vina to evaluate binding affinity between Resolvin E1 and inflammatory mediators including IL-1, GM-CSF, IFN-γ, and IL-10. In vitro analysis involved THP-1-derived macrophages stimulated with inflammatory cues and treated with Resolvin E1. Gene expression of M1 and M2 macrophage markers was assessed using qPCR. Results: Resolvin E1 demonstrated moderate binding affinity with IL-1 and GM-CSF and stable hydrogen bonding interactions. Preliminary in silico findings suggest favorable immunomodulatory potential. In vitro results are currently under evaluation. Conclusions: Resolvin E1 shows promise as a potential therapeutic modulator for controlling inflammation-mediated root resorption through macrophage polarization pathways.

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Publication Details

Journal
Indian Journal of Dental Research
Published
2026-03-01
DOI
https://doi.org/10.4103/ijdr_202637s1_abs_96
Primary Topic
Immune cells in cancer
Type
article
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article

Role of Resolvin E1 in macrophage polarization as a therapeutic strategy for root resorption: In silico and in vitro analysis

Nandini Suresh, Alan M. Punnoose
Indian Journal of Dental Research
Immune cells in cancer
article

Role of Resolvin E1 in macrophage polarization as a therapeutic strategy for root resorption: In silico and in vitro analysis

Nandini Suresh, Alan M. Punnoose
article en

Abstract

Objectives: This study aimed to evaluate the interaction of Resolvin E1 with macrophage-associated inflammatory markers and assess its potential role in macrophage polarization relevant to root resorption therapy. Methods: Molecular docking was performed using AutoDock Vina to evaluate binding affinity between Resolvin E1 and inflammatory mediators including IL-1, GM-CSF, IFN-γ, and IL-10. In vitro analysis involved THP-1-derived macrophages stimulated with inflammatory cues and treated with Resolvin E1. Gene expression of M1 and M2 macrophage markers was assessed using qPCR. Results: Resolvin E1 demonstrated moderate binding affinity with IL-1 and GM-CSF and stable hydrogen bonding interactions. Preliminary in silico findings suggest favorable immunomodulatory potential. In vitro results are currently under evaluation. Conclusions: Resolvin E1 shows promise as a potential therapeutic modulator for controlling inflammation-mediated root resorption through macrophage polarization pathways.

Indian Journal of Dental ResearchVol. 37(Suppl 1)
Meenakshi Academy of Higher Education and Research (IN)
Openalex Percentile: Top 6%
Immune cells in cancer
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