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Autophagy under the microscope as never before

We don’t tend to wrap our recycling waste in bubble wrap but that’s essentially what cells do during the cellular recycling process called autophagy. Using the live imaging capabilities at the ����������̳, Institute researchers and their collaborators at Carl Zeiss Microscopy, Munich, and the Francis Crick Institute, London, have viewed the earliest stages of this encapsulation and recycling process in super resolution to reveal what’s happening in unprecedented molecular detail. Their research is published today in the journal .
 
Derived from the Greek and meaning ‘self-eating’, describes a process whereby cellular contents are collected and recycled into new molecules and cellular structures; a process of reclaiming the unwanted or damaged and using them to create something useful for the cell. Autophagy is fundamental to the function of our bodies. As the clean-up mechanism for cellular debris, loss of efficiency or glitches in this process are associated with ageing and ageing-related diseases such as Alzheimer’s, rheumatoid arthritis and cancer.
 
The researchers focused on determining the origin and formation of a structure only seen at the very start of the autophagy process but which gives rise to the main structure (autophagosome; the cellular ‘bubble wrap’) that envelops the content targeted for degradation. Due to its short-lived nature, this transient structure was difficult to characterise. The researchers jointly developed a new comprehensive imaging-based approach for observing autophagy-related structures. At the ����������̳ this was achieved using live imaging followed by dStorm (direct Stochastic Optical Reconstruction Microscopy). At the Francis Crick Institute in London and the Zeiss Microscopy Labs in Munich, the researchers used a method called FIB-SEM (Focused Ion Beam Scanning Electron Microscopy). By combining the information gathered from these two methods, the researchers were able to identify how the first autophagy structure forms and clarify the protein and membrane associations leading to its development into a fully-fledged autophagosome.
 
, group leader in the research programme at the ����������̳ and lead senior author, said: “By combining live imaging with cutting-edge super resolution microscopy techniques, we have been able to characterise the site of autophagy initiation and observe the physical and functional interactions between the proteins involved in autophagy. This has uncovered a new level of detail of the earliest stages of autophagy and provides a general protocol for this type of analysis in other areas of cell biology.
 
“Knowing more about this process increases our ability to find ways to manipulate or boost it for future therapeutic benefit.”
 
This work was supported by the Biotechnology and Biological Sciences Research Council.
 

Image description:

A comparison of the increased level of cellular detail provided by employing dStorm microscopy (top) versus conventional methods (bottom). The green fluorescence shows the location of an autophagy-related protein involved in the early stages of autophagosome formation and red fluorescence identifies the cell’s endoplasmic reticulum. Blending the STORM and wide-field images demonstrates the resolution enhancement achieved using STORM super resolution microscopy which yields novel information on the developing pre-autophagosomal structure.
 

Publication reference:

Related publication:

Walker, Karanasios & Ktistakis. Correlative live cell and super resolution imaging of autophagosome formation. Methods in Enzymology (in press)
 

Affiliated authors (in author order):

Eleftherios Karanasios, postdoctoral researcher (Ktistakis group)
, Head of the
Hanneke Okkenhaug, Imaging Facility
Maria Manifava, postdoctoral researcher (Ktistakis group)
Qashif Ahmed, PhD student (Ktistakis group)
, group leader, research programme