Morphological and proteomic analyses reveal that unsaturated guluronate oligosaccharide modulates multiple functional pathways in murine macrophage RAW264.7 cells

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Abstract

Alginate is a natural polysaccharide extracted from various species of marine brown algae. Alginate-derived guluronate oligosaccharide (GOS) obtained by enzymatic depolymerization has various pharmacological functions. Previous studies have demonstrated that GOS can trigger the production of inducible nitric oxide synthase (iNOS)/nitric oxide (NO), reactive oxygen species (ROS) and tumor necrosis factor (TNF)-α by macrophages and that it is involved in the nuclear factor (NF)-κB and mitogen-activated protein (MAP) kinase signaling pathways. To expand upon the current knowledge regarding the molecular mechanisms associated with the GOS-induced immune response in macrophages, comparative proteomic analysis was employed together with two-dimensional electrophoresis (2-DE), matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF/TOF MS) and Western blot verification. Proteins showing significant differences in expression in GOS-treated cells were categorized into multiple functional pathways, including the NF-κB signaling pathway and pathways involved in inflammation, antioxidant activity, glycolysis, cytoskeletal processes and translational elongation. Moreover, GOS-stimulated changes in the morphologies and actin cytoskeleton organization of RAW264.7 cells were also investigated as possible adaptations to GOS. This study is the first to reveal GOS as a promising agent that can modulate the proper balance between the pro- and anti-inflammatory immune responses, and it provides new insights into pharmaceutical applications of polysaccharides.

Figures

  • Figure 1. The infrared (IR) spectrum of polyguluronic acid (PG). The spectrum was run in KBr pellets with 1 mg of sample and 200 mg of KBr.
  • Figure 2. The electrospray ionization mass spectrometry (ESI-MS) of guluronate oligosaccharide (GOS). The spectrum was acquired in the negative ion mode with a high-resolution hybrid time-of-flight mass spectrometer. The ions were present in the form of [M + xNa(K) − (x + n)H]n−. The corresponding molecular weights and DP were then calculated using the monoisotopic peaks and charge states of each group of ions.
  • Table 1. Ions observed in the mass spectrometry (MS) analysis of GOS.
  • Figure 3. (A) A representative two-dimensional electrophoresis (2-DE) gel showing of total proteins from untreated and GOS-treated RAW264.7 cells. Each gel is representative of three independent replicates. Differentially regulated proteins (≥2.0-fold) are indicated by arrows and numbers and are listed in Table 2; (B) Magnified image of an identified protein spot.
  • Table 2. Detailed information regarding the differentially expressed proteins detected by MS.
  • Figure 4. Western blot analysis of altered proteins in GOS-treated RAW264.7 cells. A representative result of three independent experiments is shown. Typical experiment conducted three times with similar results. β-tubulin was used as an internal control.
  • Figure 5. Cont.
  • Figure 5. Effects of GOS on the morphology and actin organization of RAW264.7 cells. RAW264.7 cell morphology was observed by dark-field and confocal microscopy (×40). The cells were treated with or without 1 mg/mL GOS for 24 h. Representative dark-field images and analysis results show that GOS induced morphological changes in RAW264.7 cells, including an increase in the cell number (A,B), larger cell sizes (C,D), extended nucleus areas (E,F), and a greater number of dual-nuclei cells (G,H), compared with untreated cells (control). F-actin was stained with FITC-phalloidin. GOS-induced F-actin organization was examined using fluorescence images (I) and quantitative analysis (J). Scale bar, 20 µm. All images were analyzed with ImageJ software. ** p < 0.01 and *** p < 0.001 indicate significant differences between the control group and the GOS-treated group.

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Xu, X., Bi, D. C., Li, C., Fang, W. S., Zhou, R., Li, S. M., … Shen, L. M. (2015). Morphological and proteomic analyses reveal that unsaturated guluronate oligosaccharide modulates multiple functional pathways in murine macrophage RAW264.7 cells. Marine Drugs, 13(4), 1798–1818. https://doi.org/10.3390/md13041798

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