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Complementation of Splicing Activity by a Galectin-3 - U1 snRNP Complex on Beads
Published on: December 9, 2020
Galectin-9 interacts with Vamp-3 to regulate cytokine secretion in dendritic cells
Rui Santalla Méndez1,2,3, Andrea Rodgers Furones1, René Classens1
1Department of Medical BioSciences, Radboud University Medical Center, Geert Grooteplein 26-28, 6525 GA, Nijmegen, The Netherlands.
Insights
Galectin-9 is crucial for transporting cytokines within dendritic cells (DCs). Without it, cytokine vesicles are degraded, impairing immune responses and cellular homeostasis. This reveals galectin-9
Area of Science:
- Cell Biology
- Immunology
- Molecular Biology
Background:
- Intracellular vesicle transport, mediated by SNARE proteins, is vital for cellular homeostasis.
- Endosomal trafficking to the plasma membrane is critical for cytokine secretion in dendritic cells (DCs) and initiating immune responses.
- The molecular regulators of DC cytokine secretion remain poorly understood.
Purpose of the Study:
- To investigate the intracellular roles of galectin-9 in regulating immune cell homeostasis and vesicle transport.
- To determine galectin-9's function in intracellular cytokine trafficking within primary human dendritic cells.
Main Methods:
- Investigated galectin-9 function in primary human dendritic cells (DCs).
- Utilized immunoprecipitation-mass spectrometry to identify molecular interactions.
- Assessed the impact of galectin-9 depletion on vesicle trafficking and cytokine secretion.
Main Results:
- Galectin-9 is essential for intracellular cytokine trafficking to the cell surface in DCs.
- Depletion of galectin-9 leads to accumulation and lysosomal degradation of cytokine-containing vesicles in the Golgi complex.
- Galectin-9 interacts with Vamp-3 and is required for rerouting Vamp-3-containing endosomes upon DC activation.
Conclusions:
- Galectin-9 is a necessary mechanistic component for intracellular trafficking, specifically for cytokine transport in DCs.
- This finding impacts the general understanding of vesicle transport mechanisms.
- Identifies novel roles for galectins in governing cell function and immune responses.
Abstract:
Intracellular vesicle transport is essential for cellular homeostasis and is partially mediated by SNARE proteins. Endosomal trafficking to the plasma membrane ensures cytokine secretion in dendritic cells (DCs) and the initiation of immune responses. Despite its critical importance, the specific molecular components that regulate DC cytokine secretion are poorly characterised. Galectin-9, a ß-galactoside-binding protein, has emerged as a novel cellular modulator although its exact intracellular roles in regulating (immune) cell homeostasis and vesicle transport are virtually unknown. We investigated galectin-9 function in primary human DCs and report that galectin-9 is essential for intracellular cytokine trafficking to the cell surface. Galectin-9-depleted DCs accumulate cytokine-containing vesicles in the Golgi complex that eventually undergo lysosomal degradation. We observed galectin-9 to molecularly interact with Vamp-3 using immunoprecipitation-mass-spectrometry and identified galectin-9 was required for rerouting Vamp-3-containing endosomes upon DC activation as the underlying mechanism. Overall, this study identifies galectin-9 as a necessary mechanistic component for intracellular trafficking. This may impact our general understanding of vesicle transport and sheds new light into the multiple roles galectins play in governing cell function.
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