# Toll-like Receptor Activation Remodels the Polyamine and Tryptophan Metabolism in Porcine Macrophages

**Authors:** Meimei Zhang, Lingfei Du, Yinhao Shen, Peng Bin

PMC · DOI: 10.3390/metabo15030162 · Metabolites · 2025-03-01

## TL;DR

This study shows how activating toll-like receptors in pig macrophages changes their metabolism of polyamines and tryptophan, which could help improve piglet immunity through nutrition.

## Contribution

The study reveals novel metabolic reprogramming in porcine macrophages upon TLR activation, specifically in polyamine and tryptophan pathways.

## Key findings

- TLR activation inhibits spermine production and shifts tryptophan metabolism toward kynurenic acid synthesis.
- TLR9 activation specifically redirects tryptophan metabolism, inhibiting melatonin production via PKA/cAMP/CREB pathways.
- These metabolic changes offer potential strategies for nutritional interventions to enhance piglet immunity.

## Abstract

Background: The early nutritional metabolism of piglets is intimately associated with the regulation of immune function, and amino acids play a crucial role in modulating the fate and function of porcine immune cells, especially macrophages. However, the metabolic changes upon macrophage activation remain elusive. Methods: We established an in vitro activation model of porcine macrophages and investigated alterations in metabolites involved in polyamine and tryptophan metabolism upon activation by various toll-like receptor (TLR) activators. Results: TLR activation inhibits the production of spermine and alters the kynurenine pathway of the tryptophan metabolism toward the kynurenic acid biosynthesis. Specifically, TLR9 activation redirects the metabolic pathway of tryptophan toward kynurenic acid synthesis, which subsequently inhibits melatonin production via the protein kinase A (PKA)/cyclic adenosine monophosphate (cAMP)/cAMP-responsive element-binding protein (CREB) signaling pathways. Conclusions: TLR activation reprograms the polyamine and tryptophan metabolism in porcine macrophages. Knowledge of the metabolic alterations in polyamine and tryptophan upon TLR activation in macrophages offers valuable insights and potential strategies for nutritional intervention to enhance piglet immunity.

## Linked entities

- **Chemicals:** spermine (PubChem CID 1103), kynurenine (PubChem CID 846), kynurenic acid (PubChem CID 3845), melatonin (PubChem CID 896)
- **Species:** Sus scrofa (taxon 9823)

## Full-text entities

- **Genes:** CREB1 (cAMP responsive element binding protein 1) [NCBI Gene 1385] {aka CREB, CREB-1}, TLR9 (toll like receptor 9) [NCBI Gene 54106] {aka CD289}, CAMP (cathelicidin antimicrobial peptide) [NCBI Gene 820] {aka CAP-18, CAP18, CRAMP, FALL-39, FALL39, HSD26}
- **Chemicals:** melatonin (MESH:D008550), Polyamine (MESH:D011073), kynurenic acid (MESH:D007736), spermine (MESH:D013096), kynurenine (MESH:D007737), Tryptophan (MESH:D014364)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11944168/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC11944168/full.md

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Source: https://tomesphere.com/paper/PMC11944168