The multicellular biobots can move around and help heal “wounds” created in plated neurons
Mike Silver / Tufts University Communications
(MEDFORD, Mass.) – Researchers have created tiny biological robots, called Anthrobots, from adult human tracheal cells that can move across a surface and encourage the growth of neurons in a lab dish. The multicellular assemblies, ranging in size from the width of a human hair to the point of a sharpened pencil, are designed to carry out tasks depending on the functions of their individual cells and how they work together. The discovery is a starting point for the researchers’ vision to use Anthrobots as new therapeutic tools for regeneration, healing, and treatment of disease.
The work follows earlier research in the laboratories of Michael Levin, Ph.D., Associate Faculty member of Harvard University’s Wyss Institute for Biologically Inspired Engineering and the Vannevar Bush Professor of Biology at Tufts University School of Arts & Sciences, and Josh Bongard, Ph.D. at the University of Vermont in which they created multicellular biological robots from frog embryo cells called Xenobots, capable of navigating passageways, collecting material, recording information, healing themselves from injury, and even replicating for a few cycles on their own. At that time, it was not known if these capabilities were dependent on their being derived from an amphibian embryo, or if “biobots” could be constructed from cells of other species.
In the current study published in Advanced Science, Levin, along with PhD student Gizem Gumuskaya discovered that biobots can in fact be created from adult human cells, without any genetic modification and they are demonstrating some capabilities beyond what was observed with the Xenobots. The discovery starts to answer a broader question that the lab has posed – what are the rules that govern how cells assemble and work together in the body, and can the cells be taken out of their natural context and recombined into different “body plans” to carry out other functions by design?
In this case, they gave human cells, after decades of quiet life in the trachea, a chance to reboot and find ways of creating new structures and completing tasks. “We wanted to probe what cells can do besides create default features in the body,” said Gumuskaya, who earned a degree in architecture before coming into biology. By reprogramming interactions between cells, new multicellular structure can be created, analogous to the way stone and brick can be arranged into different structural elements like walls, archways or columns.” The researchers found that not only could the cells create new multicellular shapes, but they could move in different ways over a surface of human neurons grown in a lab dish and encourage new growth to fill in gaps caused by scratching the layer of cells.
Exactly how the Anthrobots encourage growth of neurons is not yet clear, but the researchers confirmed that neurons grew under the area covered by a clustered assembly of Anthrobots which they called a “superbot.”
“The cellular assemblies we construct in the lab can have capabilities that go beyond what they do in the body,” said Levin, who also serves as the director of the Allen Discovery Center at Tufts. “It is fascinating and completely unexpected that normal patient tracheal cells, without modifying their DNA, can move on their own and encourage neuron growth across a region of damage,” said Levin. “We’re now looking at how the healing mechanism works, and asking what else these constructs can do.”
The advantages of using human cells include the ability to construct biobots from a patient’s own cells to perform therapeutic work without the risk of triggering an immune response or requiring immunosuppressants. They only last a few weeks before breaking down, and so can easily be re-absorbed into the body after their work is done.
In addition, outside of the body, Anthrobots can only survive in very specific laboratory conditions, and there is no risk of exposure or unintended spread outside the lab. Likewise, they do not reproduce, and they have no genetic edits, additions or deletions, so there is no risk of their evolving beyond existing safeguards.
How are Anthrobots made?
Each Anthrobot starts out as a single cell, derived from an adult donor. The cells come from the surface of the trachea and are covered with hairlike projections called cilia that wave back and forth. The cilia help the tracheal cells push out tiny particles that find their way into air passages of the lung. We all experience the work of ciliated cells when we take the final step of expelling the particles and excess fluid by coughing or clearing our throats. Earlier studies by other labs had shown that when the cells are grown in the lab, they spontaneously form tiny multicellular spheres called organoids.
The researchers developed growth conditions that encouraged the cilia to face outward on organoids. They noted different shapes and types of movement – the first important feature observed of the biorobotics platform. By adding other features contributed by different cells, the Anthrobots could be designed to travel through and perform functions in the body, or help build engineered tissues in the lab.
The team, with the help of Simon Garnier at the New Jersey Institute of Technology, characterized the different types of Anthrobots that were produced. They observed that bots fell into a few discrete categories of shape and movement, ranging in size from 30 to 500 micrometers (from the thickness of a human hair to the point of a sharpened pencil), filling an important niche between nanotechnology and larger engineered devices.
Some were spherical and fully covered in cilia, and some were irregular or football shaped with more patchy coverage of cilia, or just covered on one side. They traveled in straight lines, moved in tight circles, combined those movements or just sat around and wiggled. The spherical ones fully covered with cilia tended to be wigglers. The Anthrobots with cilia distributed unevenly tended to move forward for longer stretches in straight or curved paths. They usually survived about 45-60 days in laboratory conditions before they naturally biodegraded.
“Anthrobots self-assemble in the lab dish,” said Gumuskaya, who created the Anthrobots. “Unlike Xenobots, they don’t require tweezers or scalpels to give them shape, and we can use adult cells – even cells from elderly patients – instead of embryonic cells. It’s fully scalable – we can produce swarms of these biobots in parallel, which is a good start for developing a therapeutic tool.”
Because Levin and his team ultimately plan to make Anthrobots with therapeutic applications, they created a lab test to see how the biobots might heal wounds. The model involved growing a two-dimensional layer of neurons derived from neural stem cells, and simply by scratching the layer with a thin metal rod, to create an open “wound” devoid of cells.
To ensure the wound would be exposed to a dense concentration of Anthrobots, they created “superbots” – a cluster that naturally forms when the Anthrobots are confined to a small space. The superbots were made up primarily of circlers and wigglers, so they would not wander too far away from the open wound.
Although it might be expected that genetic modifications of Anthrobot cells would be needed to help the biobots encourage neural growth, surprisingly the unmodified Anthrobots triggered substantial regrowth, creating a bridge of neurons as thick as the rest of the healthy cells on the plate. Neurons did not grow in the wound where the Anthrobots were absent. At least in the simplified 2D world of the lab dish, the Anthrobot assemblies encouraged efficient healing of live neural tissue.
According to the researchers, further development of the biobots could lead to other applications, including clearing plaque buildup in the arteries of atherosclerosis patients, repairing spinal cord or retinal nerve damage, recognizing bacteria or cancer cells, or delivering drugs to targeted tissues. The Anthrobots could in theory assist in healing tissues, while also laying down pro-regenerative drugs.
Making new blueprints, restoring old ones
Gumuskaya explained that cells have the innate ability to self-assemble into larger structures in certain fundamental ways. “The cells can form layers, fold, make spheres, sort and separate themselves by type, fuse together, or even move,” she said. “Two important differences from inanimate bricks are that cells can communicate with each other and create these structures dynamically, and each cell is programmed with many functions, like movement, secretion of molecules, detection of signals and more. We are just figuring out how to combine these elements to create new biological body plans and functions – different than those found in nature.”
Taking advantage of the inherently flexible rules of cellular assembly helps the scientists construct the biobots, but it can also help them understand how natural body plans assemble, how the genome and environment work together to create tissues, organs and limbs, and how to restore them with regenerative treatments.
This research was supported by Astonishing Labs and grant 62212 from the John Templeton Foundation.