Summary of project PR002549
This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR002549. The data can be accessed directly via it's Project DOI: 10.21228/M8583B This work is supported by NIH grant, U2C- DK119886.
See: https://www.metabolomicsworkbench.org/about/howtocite.php
| Project ID: | PR002549 |
| Project DOI: | doi: 10.21228/M8583B |
| Project Title: | In Vitro Method Demonstrating Trained Immunity as a Distinctive Functional Program: Implications for Biomarker Discovery, Adaptive Immune Responses, Sample Cryopreservation, and Mouse Genetics |
| Project Summary: | Trained immunity is a distinct program of macrophages, enabling them to secrete varying levels of inflammatory cytokines according to their functional state during sequential stimulation. Experimental models that accurately replicate the defining steps of trained immunity are urgently needed. Here, we developed an in vitro methodology to study trained immunity using murine bone marrow-derived macrophages stimulated with β-glucan and lipopolysaccharide (LPS). Longitudinal analysis of interleukin 6 (IL6) and tumor necrosis factor (TNF) production demonstrated that trained macrophages secrete higher cytokine levels following primary stimulation with β-glucancompared to unstimulated macrophages (step 1). After a resting period, trained macrophages return to basal levels of cytokine production (step 2) but rapidly produce enhanced levels of IL6 and TNF after secondary stimulation with LPS, compared to macrophages individually stimulated with either β-glucan (step 3) or LPS (step 4) alone. The combined cytokine production of macrophages after single stimulation with βglucan (stimulus 1) and LPS (stimulus 2) was significantly lower than the cytokine levels produced by trained macrophages sequentially stimulated with both β-glucan and LPS (stimulus 1+2) (step 5). These results experimentally reproduce, for the first time, the distinctive functional stages that macrophages undergo during the training process. Using this methodology, we identified serum amyloid A3 protein (SAA3) as a novel biomarker of trained immunity and revealed that trained macrophages induce T-cell proliferation via a contact dependent mechanisms. Additionally, our results uncovered adverse effects of cell cryopreservation, strain-specific differences, and the impact of mTOR genetic ablation in the induction of trained immunity. Standardization of methodologies to study trained immunity is critical for advancing our understanding of the fundamental mechanisms that regulate innate immune memory responses and develop therapies that specifically target trained immunity in multiple immune-mediated pathological conditions. |
| Institute: | Instituto de Salud Carlos III |
| Last Name: | Arranz Herrero |
| First Name: | Javier |
| Address: | Dalia 52, Mostoles, Madrid, 28933, Spain |
| Email: | j.arranz3@usp.ceu.es |
| Phone: | 655653445 |
Summary of all studies in project PR002549
| Study ID | Study Title | Species | Institute | Analysis(* : Contains Untargted data) | Release Date | Version | Samples | Download(* : Contains raw data) |
|---|---|---|---|---|---|---|---|---|
| ST004061 | In Vitro Method Demonstrating Trained Immunity as a Distinctive Functional Program: Implications for Biomarker Discovery, Adaptive Immune Responses, Sample Cryopreservation, and Mouse Genetics | Mus musculus | Instituto de Salud Carlos III | MS | 2025-08-14 | 1 | 24 | Uploaded data (38.1M)* |
