New mechanism of cell movement identified and imaged for the first time.
Cells have finger-like projections that they use to feel their surroundings. They can detect the chemical environment and they can ‘feel’ their physical surroundings using ultrasensitive sensors. New research from the Niels Bohr Institute shows how the finger-like structures, called filopodia can extend themselves, contract and bend in dynamic movements. The results are published in the journal, Proceedings of the National Academy of Sciences.
In many biological processes, cell interaction and communication with their environment are critical to their functioning. To feel their surroundings, the cells use finger-like structures that are actually tube-like protrusions from the cell membrane. These tubes are called filopodia and they can bring messages back to the cell about both the chemical environment and the physical surroundings. Fore example, the cells use the filopodia structures for correct development of the embryo, for growing nerve cells and when cells (like macrophages) need to migrate towards pathogenic bacteria in order to remove them.
The filopodia structures are very dynamic and can both contract and elongate and bend actively in all directions. But what is it that allows them to move, how do they control their movements and what forces do they use? This is what the team wanted to find out.
The researchers studied the physical properties of filopodia using an optical trap, which is a microscope that can influence individual living cells using a highly focused laser while the researcher observes, measures and follows their movements.
In order to follow the movements better, the researchers placed a small plastic ball on the tip of the filopodia structure and by performing ultrasensitive force measurements, they could measure the dynamic activity in the individual filopodia. In addition to the force measurements, the internal ‘skeleton’ of the filopodia, called actin, which is responsible for the movement of the filopodia, was marked with fluorescent markers in order to monitor the movements in the microscope.
In the experiment the researchers grasped the ball sitting on the end of the filopodia antenna and pulled it with the ultrasensitive force microscope for up to 20 minutes. The team measured cells being ‘pulled back’ with a force of 1-100 piconewtons, the equivalent of the gravity on a single red blood cell.
Furthermore, the study revealed a new mechanism that the filopodia use to move. The team observed that the actin inside the filopodia exhibited a marked twisting motion and when it drew back, spiral folds were formed, just like when an elastic band is twisted, holding tight to one end and pulling the other.
These spiral folds were filmed using fluorescence microscopy, all while measuring the contraction. The rotational mechanism that formed the spiral in the actin structure is important for making it possible for the filopodia to explore their environment by means of the rotary movement. These new results show a surprising new mechanism where rotation is converted into a mechanical feature that makes it possible for the cell to interact with neighbouring cells.
The team state that spiral-shaped structures are found everywhere in nature, for example, it the twisted DNA strand, as well as the hair-like cilia and flagella, which are a kind of rotating helix that give some bacteria and sperm cells the ability to swim.
Spiral-shaped filopodia were previously predicted in theory, but the predictions were based on a different mechanism for spiral formation. However, these spiral-shaped folds could also be proven theoretically by modelling a rotating actin structure inside a membrane tube.
The team summise that the results show that experiments and theoretical calculations work well together when studying biological mechanisms.