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Updated: Sep 16, 2026

Using Live Cell STED Imaging to Visualize Mitochondrial Inner Membrane Ultrastructure in Neuronal Cell Models
Published on: June 30, 2023
Variations in the structure of mitochondria
Abstract:
A characteristic internal structure, consisting of a double-layered outer wall enclosing a matrix-filled space through which pass double-layered membranous folds, would appear to comprise as satisfactory a definition of mitochondria for electron microscopy as their intravital affinity for Janus green affords for light microscopy. Relying for identification upon this characteristic internal structure, mitochondria appear to be pleomorphic structures which vary in size, shape, complexity, and density. They are labile also in that their number may increase or decrease under controlled conditions. The possibility therefore exists that these organelles are constantly being formed and destroyed, perhaps by their participation in metabolic processes. The problem of the origin of mitochondria is in an unsatisfactory state. New organelles unquestionably are formed in particular physiological states. The possibility that new bodies are produced by fission of ones already present does not seem adequate. On the other hand, the possible fabrication of new mitochondria out of intracellular membranes, although an attractive hypothesis, has not been adequately substantiated.
Insights
Mitochondria, vital cell organelles, possess a distinct internal structure visible via electron microscopy. Their dynamic nature suggests constant formation and destruction, but their precise origin remains unclear.
Area of Science:
- Cell Biology
- Microscopy
- Organelle Biology
Background:
- Mitochondria are essential cellular components with a defined internal structure.
- Electron microscopy and light microscopy (using Janus green stain) are key identification methods.
- Mitochondria exhibit pleomorphism, varying in size, shape, and density.
Purpose of the Study:
- To define mitochondria based on their characteristic internal structure for electron microscopy.
- To explore the dynamic nature and potential turnover of mitochondria within cells.
- To address the unresolved question of mitochondrial origin.
Main Methods:
- Utilizing electron microscopy to identify mitochondria by their double-layered outer wall and internal membranous folds.
- Observing changes in mitochondrial number under controlled physiological conditions.
- Reviewing existing hypotheses on mitochondrial formation, including fission and de novo synthesis.
Main Results:
- A characteristic internal structure provides a reliable definition for mitochondria in electron microscopy.
- Mitochondria are labile, with numbers fluctuating, indicating dynamic processes.
- New mitochondria form in specific physiological states, but the exact origin mechanism is uncertain.
Conclusions:
- The defined internal structure is a satisfactory basis for identifying mitochondria via electron microscopy.
- The dynamic nature of mitochondria suggests continuous formation and degradation, possibly linked to metabolism.
- Current understanding of mitochondrial origin is inadequate, with neither fission nor intracellular membrane synthesis fully substantiated.
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