Related Experiment Video
Updated: Sep 16, 2026

Analyzing Mitochondrial Transport and Morphology in Human Induced Pluripotent Stem Cell-Derived Neurons in Hereditary Spastic Paraplegia
Published on: February 9, 2020
Mitochondria in living cells: an analysis of movements
Abstract:
Time-lapse cinephotomicrography of mouse embryonic fibroblasts before and shortly after perfusion of tissue cultures reveals that the elongation of mitochondria caused by coenzyme A results from the terminal association of many shorter rods into a smaller number of long filaments. These are not permanent associations, but they reflect an exaggeration of the cohesive tendency of mitochondria, which in untreated cells is counterbalanced by frequent disjoinings and breakings of the anastomotic network. Our own observations and a survey of the literature suggest that elongate mitochondria with rapid movement and high metabolic activity tend to accompany proliferation in tissue cultures, and that mitotic inhibition of cultured cells may go together with short, slow mitochondria of low metabolic activity. The movement of mitochondria may be both active, reflecting metabolic exchanges with the cytoplasm, and passive, the result of hyaloplasmic currents.
Insights
Coenzyme A causes mitochondria elongation in mouse cells by forming long filaments from shorter rods. This exaggerated cohesion, linked to cell proliferation, contrasts with inhibited cells showing short, slow mitochondria.
Area of Science:
- Cell Biology
- Mitochondrial Dynamics
- Biochemistry
Background:
- Mitochondria exhibit dynamic changes in shape and distribution within cells.
- Cellular metabolic state and proliferative activity influence mitochondrial morphology.
- Coenzyme A is a crucial molecule in cellular metabolism.
Purpose of the Study:
- To investigate the mechanism of mitochondrial elongation induced by coenzyme A.
- To correlate mitochondrial morphology and dynamics with cell proliferation and metabolic activity.
- To understand the role of mitochondrial cohesion and network dynamics.
Main Methods:
- Time-lapse cinephotomicrography of mouse embryonic fibroblasts in tissue culture.
- Observation of mitochondrial changes before and after perfusion with coenzyme A.
- Literature survey on mitochondrial behavior in relation to cell cycle and metabolism.
Main Results:
- Coenzyme A induces mitochondrial elongation through the fusion of shorter mitochondrial rods into longer filaments.
- Mitochondrial elongation reflects an exaggerated tendency for cohesion, normally balanced by network breakdown.
- Elongate, rapidly moving mitochondria correlate with cell proliferation, while short, slow mitochondria are associated with mitotic inhibition.
Conclusions:
- Mitochondrial elongation by coenzyme A is a dynamic process involving filament formation.
- Mitochondrial morphology and dynamics are closely linked to cellular metabolic state and proliferative capacity.
- Understanding these dynamics offers insights into cell cycle regulation and metabolic control.
Related Concept Videos
Mitochondria
Mitochondria
Mitochondrial Membranes
Translocation of Proteins into the Mitochondria
Sorting of outer membrane proteins:
Mitochondrial outer membrane proteins are of two types: the transmembrane, beta-barrel porins, and the membrane-anchored, alpha-helical proteins. Beta-barrel porin precursors are translocated by the TOM complex and inserted into the outer mitochondrial membrane by the SAM complex. In contrast,...
The Inner Mitochondrial Membrane
Animal Mitochondrial Genetics

