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High-intensity light disrupts intracellular organelle dynamics via microtubule depolymerization
Zihao Zhang1, Jian Han1,2, Ke Wei1
1College of Ocean and Earth Sciences, Xiamen University, Xiamen, 361102, Fujian, China.
Scientific Reports
|July 2, 2025
Summary
High-intensity white light causes pigment granule dispersion in fish cells by affecting microtubules and calcium levels. This organelle transport disruption is reversible and also observed in human cells.
Area of Science:
- Cell Biology
- Organelle Transport
- Cytoskeleton Dynamics
Background:
- Chromatophores are specialized cells for pigment granule translocation.
- Previous research linked low-intensity light-induced aggregation to Opsin 3.
- High-intensity light effects on organelle transport remain less understood.
Purpose of the Study:
- To investigate the effects of prolonged high-intensity white light (HIWL) on xanthosomes in fish chromatophores.
- To elucidate the underlying molecular mechanisms of HIWL-induced xanthosome dispersion.
- To determine if this mechanism is conserved in other cell types.
Main Methods:
- Exposure of fish xanthophores to prolonged HIWL (10,000 lux).
- Ex vivo illumination and pharmacological treatments.
- Analysis of intracellular calcium levels and microtubule dynamics.
- Experiments on human cell lines (HeLa, HEK293T) under HIWL.
Main Results:
- HIWL induces reversible xanthosome dispersion, distinct from low-intensity aggregation.
- Dispersion is mediated by microtubule depolymerization due to elevated intracellular Ca2+ from IP3R channels.
- This mechanism is also observed in HeLa and HEK293T cells exposed to HIWL.
Conclusions:
- HIWL triggers organelle dispersion via a novel Ca2+- and microtubule-dependent pathway.
- This light-induced cellular response is conserved across different species and cell types.
- Findings expand understanding of high-intensity light's impact on intracellular transport and cytoskeleton.
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