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Biology subjects

Aizawa, S.

Publications and source records attributed to Aizawa, S..

3 recordsLinked to original sources

Organelle-Specific pH Quantification Using a Protein-Based Quantum Sensor

Quantum sensing enables measurements of physicochemical changes within living cells at the organelle level. Conventional nanoparticle-based sensors, however, face limitations in subcellular targeting, intracellular tracking, and following dynamic biological processes across distinct intracellular environments. Here, we investigate MagLOV2, a genetically encoded quantum sensor, by examining its organelle-specific localization, magnetic field effects (MFEs) during mitophagy, and pH dependent response kinetics. MagLOV2 retained magnetic responsiveness in the cytoplasm, nucleus, and mitochondria, with fluorescence contrasts of 17.1%, 12.3%, and 28.0%, respectively. Optimization of mitochondrial targeting increased fluorescence 2.7 fold. During CCCP induced mitophagy, lysosomal colocalization of MagLOV2 increased from 20.75% to 89.73%, accompanied by slower MFE responses in acidic compartments. Purified MagLOV2 showed response times ranging from 8.27 s at pH 4.5 to 1.56 s at pH 9.5. Structural, spectral, and kinetic analyses suggested that protonation dependent flavin photochemistry and the surrounding protein environment contribute to this behavior. These measurements demonstrate that genetically targeted MagLOV2 can follow organelle transport and report local acidification through changes in magnetic-response kinetics.

biophysics↗

The lysosomal membrane protein LAMP2B mediates microlipophagy to target obesity-related disorders

Lifestyle diseases, such as obesity, diabetes, and metabolic syndrome, are leading health problems, most of which are related to abnormal lipid metabolism. Lysosomes can degrade lipid droplets (LDs) via microautophagy. Here, we report the molecular mechanism and pathophysiological roles of microlipophagy, regulated by the lysosomal membrane protein LAMP2B. Our study revealed that LAMP2B interacts with phosphatidic acid, facilitating lysosomal-LD interactions and enhancing lipid hydrolysis via microlipophagy depending on endosomal sorting complexes required for transport. Correlative light and electron microscopy demonstrated direct LDs uptake into lysosomes at contact sites. Moreover, LAMP2B overexpression in mice prevents high-fat diet-induced obesity, insulin resistance, and adipose tissue inflammation; liver lipidomics analysis suggested enhanced triacylglycerol hydrolysis. Overall, the findings of this study elucidated the mechanism of microlipophagy, which could be promising for the treatment of obesity and related disorders.

cell biology↗

Deletion of class II ARF causes essential tremors through Nav1.6 traffic impairment

ADP-ribosylation factors (ARFs) are a family of small monomeric GTPases consisting of three classes. In the present study, we generated class II ARF-deficient mice (ARF4+/-/ARF5-/-) and found that they exhibited severe movement-associated tremors. Treatment of the mice with propranolol and gabapentin, which alleviate symptoms in patients with essential tremors, similarly reduced the amplitude of the pathologic tremors. In vivo electrophysiological recordings of the ARF4+/-/ARF5-/- mice revealed that they exhibited reduced excitability of their cerebellar Purkinje cells. Immunohistochemical studies revealed that ARF4+/-/ARF5-/- mice exhibit a severe, selective reduction of Nav1.6 proteins that are important for maintaining repetitive action potential firing in the axon initial segments (AISs) of the Purkinje cells. This decrease in Nav1.6 protein expression and the consequent tremors were alleviated by Purkinje cell-specific expression of ARF5. These results indicate that class II ARF mediates the selective trafficking of Nav1.6 to the AISs in cerebellar Purkinje cells, and suggest that the essential tremors can be ascribed to the reduced intrinsic excitability of Purkinje cells, caused by the selective decrease of Nav1.6 proteins in the AISs.

neuroscience↗