PA-GFP: a window into the subcellular adventures of the individual mitochondrion
Sarah E Haigh1, Gilad Twig, Anthony A J Molina
1Department of Pharmacology and Experimental Therapeutics, Tufts University School of Medicine, 136 Harrison Ave, Boston, MA 02111, USA.
Abstract:
Mitochondrial connectivity is characterized by matrix lumen continuity and by dynamic rewiring through fusion and fission events. While these mechanisms homogenize the mitochondrial population, a number of studies looking at mitochondrial membrane potential have demonstrated that mitochondria exist as a heterogeneous population within individual cells. To address the relationship between mitochondrial dynamics and heterogeneity, we tagged and tracked individual mitochondria over time while monitoring their mitochondrial membrane potential (deltapsi(m)). By utilizing photoactivatible-GFP (PA-GFP), targeted to the mitochondrial matrix, we determined the boundaries of the individual mitochondrion. A single mitochondrion is defined by the continuity of its matrix lumen. The boundaries set by luminal continuity matched those set by electrical coupling, indicating that the individual mitochondrion is equipotential throughout the entire organelle. Similar results were obtained with PA-GFP targeted to the inner membrane indicating that matrix continuity parallels inner membrane continuity. Sequential photoconversion of matrix PA-GFP in multiple locations within the mitochondrial web reveals that each ramified mitochondrial structure is composed of juxtaposed but discontinuous units. Moreover, as many as half of the events in which mitochondria come into contact, do not result in fusion. While all fission events generated two electrically uncoupled discontinuous matrices, the two daughter mitochondria frequently remained juxtaposed, keeping the tubular appearance unchanged. These morphologically invisible fission events illustrate the difference between mitochondrial fission and fragmentation; the latter representing the movement and separation of disconnected units. Simultaneous monitoring of deltapsi(m) of up to four individual mitochondria within the same cell revealed that subcellular heterogeneity in deltapsi(m) does not represent multiple unstable mitochondria that appear 'heterogeneous' at any given point, but rather multiple stable, but heterogeneous units.
Insights
Mitochondria maintain stable, heterogeneous membrane potentials despite dynamic fusion and fission. Individual mitochondria are equipotential, but cell populations show distinct, stable mitochondrial units.
Area of Science:
- Cell Biology
- Mitochondrial Dynamics
- Membrane Potential
Background:
- Mitochondrial connectivity relies on matrix lumen continuity and dynamic fusion/fission events.
- Studies show mitochondrial membrane potential (deltapsi(m)) is heterogeneous within cells, contrasting with homogenization mechanisms.
Purpose of the Study:
- To investigate the relationship between mitochondrial dynamics (fusion/fission) and observed heterogeneity in mitochondrial membrane potential.
- To determine if individual mitochondria are equipotential and how dynamics influence population heterogeneity.
Main Methods:
- Utilized photoactivatible-GFP (PA-GFP) targeted to the mitochondrial matrix and inner membrane to define individual mitochondrial boundaries.
- Tracked individual mitochondria over time, monitoring mitochondrial membrane potential (deltapsi(m)).
- Performed sequential photoconversion of PA-GFP in multiple locations within the mitochondrial network.
Main Results:
- Individual mitochondria are equipotential, with matrix and inner membrane continuity defining single units.
- Many mitochondrial contacts do not result in fusion; fission events create electrically uncoupled but often juxtaposed daughter mitochondria.
- Cellular heterogeneity in deltapsi(m) arises from multiple stable, yet distinct, mitochondrial units, not transient instability.
Conclusions:
- Mitochondrial dynamics, particularly fission, can generate stable, heterogeneous populations of mitochondria within a single cell.
- The equipotential nature of individual mitochondria contrasts with the stable, subcellular heterogeneity of membrane potential observed.
- Distinguishes between mitochondrial fission and fragmentation, highlighting the role of stable units in cellular bioenergetics.
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