Microtubules, assemble!

New research may lead to better understanding of self-organization in cells

What bones are to bodies, the cytoskeleton is to cells. The cytoskeleton maintains cellular structure, builds appendages like flagella and, together with motor proteins, powers cellular movement, transport, and division. Microtubules are a critical component of the cytoskeleton, vital for cell division and, because of that, an excellent target for chemotherapy drugs.

Microtubules can spontaneously self-organize, transforming from many singular components into one large cellular structure capable of performing specific tasks. Think Transformers. How they do that, however, has remained unclear.

Now, researchers at the Harvard John A. Paulson School of Engineering and Applied Sciences (SEAS) have observed how microtubules and motor proteins assemble into macroscopic networks. Their observation provides a better understanding of cytoskeletal self-organization in general, which may in turn lead to better drug design and new materials that can mimic cellular behaviors.

The research was recently published in the journal eLife.

Spindles are cellular structures that play an important role in cell division, separating chromosomes and pulling the duplicated DNA from the mother cell into the daughter cell. They are made up of microtubules and many other proteins, including the motor protein dynein.

“What we are really looking for is a grand unified theory of spindle assembly,” said Peter Foster, a graduate student at SEAS and the paper’s first author.  “We know how motor proteins interact with microtubules but how do you go from individual microtubules and motor proteins to large networked structures?”

To gain insight into how spindles assemble, Foster and his team, under the leadership of Dan Needleman, associate professor of applied physics and of molecular and cellular biology, built a simple experiment. They extracted cytoplasm from frog eggs, which contains dynein and all of the components needed to make spindles, added fluorescent protein and the chemotherapy drug Taxol to create and stabilize microtubules, and loaded the mixture into “the world’s simplest microfluidic chamber.”

“Very quickly, we saw that these microtubules organize into networks that spontaneously contract,” Foster said. “The question is why?”