Mitochondria Lysosome Interaction

Mitochondria-lysosome interaction is the coordinated communication between mitochondria, which produce cellular energy, and lysosomes, which digest and recycle cellular materials. Through transient organelle contact sites and mitophagy, damaged or surplus mitochondria are identified, transported for lysosomal degradation, and linked to cellular stress, nutrient, and metabolic signaling. In neurons, where long axons and synapses depend on efficient energy production and organelle quality control, this interaction helps maintain cellular function. Disruption of mitochondrial turnover or lysosomal processing can impair neuronal survival and is associated with mechanisms relevant to neurodegenerative disease research, making the pathway an important target for understanding disease progression and potential therapies.

Mitochondria Lysosome Interaction - Related Videos

Research

JoVE Journal - Neuroscience

Dual-color Correlative Light and Electron Microscopy for the Visualization of Interactions between Mitochondria and Lysosomes

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Cited by 4 •

2024

This protocol describes a mechanism for using correlative light and electron microscopy to visualize the interaction of mitochondria and lysosomes labeled with mEosEM and APEX2, respectively.

Visualizing Mitophagy with Fluorescent Dyes for Mitochondria and Lysosome

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Cited by 4 •

2022

Mitophagy is the primary mechanism of mitochondrial quality control. However, the evaluation of mitophagy in vivo is hindered by the lack of reliable quantitative assays. Presented here is a protocol for the observation of mitophagy in living cells using a cell-permeant green-fluorescent mitochondria dye and a red-fluorescent lysosome dye.

Multicolor Flow Cytometry-based Quantification of Mitochondria and Lysosomes in T Cells

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2019

This article illustrates a powerful method to quantify mitochondria or lysosomes in living cells. The combination of lysosome- or mitochondria-specific dyes with fluorescently conjugated antibodies against surface markers allows the quantification of these organelles in mixed cell populations, like primary cells harvested from tissue samples, by using multicolor flow cytometry.

Study of Endoplasmic Reticulum and Mitochondria Interactions by In Situ Proximity Ligation Assay in Fixed Cells

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Cited by 59 •

2016

Here, we describe a procedure to visualize and quantify with high sensitivity the endogenous interactions between the endoplasmic reticulum and mitochondria in fixed cells. The protocol features an optimized in situ proximity ligation assay targeting the inositol 1,4,5-triphosphate receptor/glucose-regulated protein 75/voltage-dependent anion channel/cyclophilin D complex at the mitochondria-associated membrane interface.

Multi-parameter Measurement of the Permeability Transition Pore Opening in Isolated Mouse Heart Mitochondria

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Cited by 19 •

2012

A spectrofluorometric protocol for the measurement of the mitochondrial permeability transition pore opening in isolated mouse heart mitochondria is presented here. The assay involves the simultaneous measurement of mitochondria Ca2+ handling, mitochondrial membrane potential and mitochondrial volume. The procedure for obtaining high-quality and functional heart mitochondria is also described.

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