Pectic Polysaccharides and Glucans in Macrophage Redox-Immune Crosstalk: Structural Determinants, Receptor Signaling, and Evidence Boundaries
- 1School of Life Sciences, Zhuhai College of Science and Technology, Zhuhai 519041, China
- 2College of Life Sciences, Jilin University, Changchun 130021, China
- 3Medical Sciences Division, Macau University of Science and Technology, Macao 999078, China
Abstract
Pectic polysaccharides and glucans alter macrophage immune and redox behavior through effects that depend on polymer architecture, presentation, and cell state. This review compares named preparations by structural features, receptor signaling, and functional outcomes. Pectin domains, esterification, branching, and mass, together with glucan linkage, conformation, solubility, and particle state, shape responses across macrophage models. Measured outputs include reactive oxygen species (ROS), nitric oxide (NO), TNF-alpha, IL-6, IL-1beta, IL-12, phagocytosis, CD86/CD206 polarization markers, mitochondrial respiration, and trained immunity. TLR4, CR3, CD206, and Dectin-1 connect polymer recognition with these responses. Most mechanistic evidence comes from cultured macrophages; animal studies mainly report tissue outcomes with limited macrophage-specific attribution. Receptor perturbation and direct-binding experiments identify material-specific mechanisms, while a complete structure-to-receptor-to-redox-to-function chain remains to be established in one model. Durable trained immunity requires stimulus removal, a defined rest interval, and standardized rechallenge, supported by metabolic or epigenetic changes. Priorities are comparisons of matched polymer fractions, receptor and redox perturbations linked to functional endpoints, and in vivo tests that identify the macrophage contribution through depletion, adoptive transfer, or conditional deletion. Integrating these designs with consistent structural characterization will clarify which polymer features govern macrophage responses and how those effects transfer between experimental systems.
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BibTeX
@article{sun2026pectic,
title = {{Pectic Polysaccharides and Glucans in Macrophage Redox-Immune Crosstalk: Structural Determinants, Receptor Signaling, and Evidence Boundaries}},
author = {Henan Sun and Hao Yu and Huiqiang Yu and Runrong Zhang and Gaowa Saren and Ke Feng and Wenzhong Hu},
journal = {Biomolecules},
year = {2026},
month = nov,
doi = {10.3390/biom16111610},
url = {https://www.mdpi.com/2218-273X/16/11/1610},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Pectic Polysaccharides and Glucans in Macrophage Redox-Immune Crosstalk: Structural Determinants, Receptor Signaling, and Evidence Boundaries
AU - Henan Sun
AU - Hao Yu
AU - Huiqiang Yu
AU - Runrong Zhang
AU - Gaowa Saren
AU - Ke Feng
AU - Wenzhong Hu
PY - 2026
DA - 2026/11/04
JO - Biomolecules
DO - 10.3390/biom16111610
UR - https://www.mdpi.com/2218-273X/16/11/1610
AB - Pectic polysaccharides and glucans alter macrophage immune and redox behavior through effects that depend on polymer architecture, presentation, and cell state. This review compares named preparations by structural features, receptor signaling, and functional outcomes. Pectin domains, esterification, branching, and mass, together with glucan linkage, conformation, solubility, and particle state, shape responses across macrophage models. Measured outputs include reactive oxygen species (ROS), nitric oxide (NO), TNF-alpha, IL-6, IL-1beta, IL-12, phagocytosis, CD86/CD206 polarization markers, mitochondrial respiration, and trained immunity. TLR4, CR3, CD206, and Dectin-1 connect polymer recognition with these responses. Most mechanistic evidence comes from cultured macrophages; animal studies mainly report tissue outcomes with limited macrophage-specific attribution. Receptor perturbation and direct-binding experiments identify material-specific mechanisms, while a complete structure-to-receptor-to-redox-to-function chain remains to be established in one model. Durable trained immunity requires stimulus removal, a defined rest interval, and standardized rechallenge, supported by metabolic or epigenetic changes. Priorities are comparisons of matched polymer fractions, receptor and redox perturbations linked to functional endpoints, and in vivo tests that identify the macrophage contribution through depletion, adoptive transfer, or conditional deletion. Integrating these designs with consistent structural characterization will clarify which polymer features govern macrophage responses and how those effects transfer between experimental systems.
SN - 2218-273X
ER -