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categories: ["bodies"]categories: ["bodies"]tags: ["synthetic biology", "morphogenesis", "biorobotics", "regeneration", "self-assembly", "michael levin"]tags: ["synthetic biology", "morphogenesis", "biorobotics", "regeneration", "self-assembly", "michael levin"]summary: "Sub-millimetre motile constructs assembled from frog embryonic cells and shaped by an evolutionary algorithm, classed as neither robots nor organisms in any settled sense."summary: "Sub-millimetre motile constructs assembled from frog embryonic cells and shaped by an evolutionary algorithm, classed as neither robots nor organisms in any settled sense."updated: "2026-07-27"updated: "2026-10-29"humanEvidence: "No xenobot has been placed in an animal or a person; the human-cell version, anthrobots, has been tested only in culture dishes, including on sheets of cultured human neurons."humanEvidence: "No xenobot has been placed in an animal or a person; the human-cell version, anthrobots, has been tested only in culture dishes, including on sheets of cultured human neurons."access: "Not a product. Built in a small number of academic laboratories from frog embryos or donor-derived human airway cells; none are sold, licensed, or approved for any use."access: "Not a product. Built in a small number of academic laboratories from frog embryos or donor-derived human airway cells; none are sold, licensed, or approved for any use."reversibility: "reversible"reversibility: "reversible"lines 32–72 → 32–7417 unchanged lines not shown
}}`````` **Xenobots** are motile constructs, under a millimetre across, made by sculpting clumps of**Xenobots** are motile constructs, under a millimetre across, made by sculpting clumps of embryonicembryonic cells from the African clawed frog *Xenopus laevis* into shapes selected by ancells from the African clawed frog *Xenopus laevis* into shapes selected by an evolutionaryevolutionary algorithm running in a physics simulator. They carry no engineered hardware, noalgorithm running in a physics simulator. They carry no engineered hardware, no circuitry and nocircuitry, and no edited DNA; motion comes from beating cilia or from contracting embryonic heartedited DNA. They move by beating cilia or by contracting embryonic heart muscle, and they run onmuscle, and the energy comes from yolk the cells carried out of the egg. The first were reported inyolk the cells carried out of the egg. The first were reported in 2020 by Sam Kriegman, Douglas2020 by Sam Kriegman, Douglas Blackiston, Michael Levin and Josh Bongard, working between TuftsBlackiston, Michael Levin and Josh Bongard, working between Tufts University and the University ofUniversity and the University of Vermont.[^kriegman2020] The name joins the genus *Xenopus* to theVermont.[^kriegman2020] The name joins the genus *Xenopus* to the back half of *robot*, and thatback half of *robot*, and that second half has caused most of the trouble since.second half accounts for most of the misunderstanding since. ## How they are made## How they are made The pipeline has two halves that never touch. In the first, an evolutionary algorithm searches aThe process has two stages that do not interact. In the first, an evolutionary algorithm searches aspace of soft-body designs built from voxels of two kinds — passive tissue and contractile tissue —space of soft-body designs built from voxels of two kinds, passive tissue and contractile tissue. Itscoring each candidate in simulation on a task such as travelling in a straight line or pushing ascores each candidate in simulation on a task such as travelling in a straight line or pushing aparticle, then filtering the survivors for robustness, since a design that collapses under smallparticle, then filters the survivors for robustness, since a design that collapses under smallperturbations will not survive transfer to tissue.perturbations will not survive transfer to tissue. In the second half a person builds the winning shape by hand. Animal cap tissue is dissected fromIn the second stage a person builds the winning shape by hand. Animal cap tissue is dissected fromblastula-stage frog embryos, dissociated, and left to reaggregate into a coherent ball.blastula-stage frog embryos, dissociated, and left to reaggregate into a coherent ball.Microsurgical forceps and a cautery electrode then carve that ball to match the design, and in theMicrosurgical forceps and a cautery electrode then carve that ball to match the design, and in theoriginal constructs a graft of cardiac progenitor tissue supplies the contractions that push theoriginal constructs a graft of cardiac progenitor tissue supplies the contractions that push theobject along. Nothing is loaded into the finished construct afterwards. The design step delivers aobject along. Nothing is loaded into the finished construct afterwards: the design step delivers abody plan and stops, which is the first respect in which the word "robot" misleads.body plan and stops. That is the first respect in which the word "robot" misleads. A later generation dispensed with the surgery and the heart muscle. Animal cap cells left toA later generation dispensed with the surgery and the heart muscle. Animal cap cells left tothemselves form spheroids that place their cilia on the outside — the same cilia that wouldthemselves form spheroids that place their cilia on the outside and swim, using the same cilia thatotherwise sweep mucus across frog skin — and swim. These constructs repair themselves withinwould otherwise sweep mucus across frog skin. These constructs repair themselves within minutes ofminutes of being lacerated, mill through fields of loose particles, and can be made to record anbeing lacerated and mill through fields of loose particles. They can also be made to record anexposure to light by expressing a photoconvertible fluorescent protein, injected into the embryo asexposure to light by expressing a photoconvertible fluorescent protein, injected into the embryo asmessenger RNA rather than written into the genome.[^blackiston2021] Nothing here involvesmessenger RNA rather than written into the genome.[^blackiston2021] No[[crispr-cas9|genome editing]]: the cells carry the frog's ordinary genome in an unfamiliar setting.[[crispr-cas9|genome editing]] is involved at any point; the cells carry the frog's ordinary genomein an unfamiliar setting. Lifespan is set by the maternally loaded yolk platelets the cells inherited. Unfed, the ciliatedLifespan is set by the maternally loaded yolk platelets the cells inherited. Unfed, the ciliatedconstructs move for roughly ten days and then break down; in frog culture medium they have been keptconstructs move for roughly ten days and then break down. In frog culture medium they have been keptalive for months, since the cells retain ordinary metabolic machinery. None can find its own food.alive for months, because the cells retain ordinary metabolic machinery, but none can find its ownfood. ## Development history## Development history lines 84–198 → 86–20411 unchanged lines not shown
## Kinematic self-replication## Kinematic self-replication The 2021 report that xenobots "self-replicate" is the most misread result in theThe 2021 report that xenobots "self-replicate" is the most misread result in thefield.[^kriegman2021] What was observed is mechanical. A parent construct swimmingfield.[^kriegman2021] The observed process is mechanical. A parent construct swimming through a dishthrough a dish strewn with dissociated stem cells pushes them into heaps; a heap that reaches astrewn with dissociated stem cells pushes them into heaps; a heap that reaches a threshold sizethreshold size compacts, grows cilia, and swims off as a new construct. An evolutionary search foundcompacts, grows cilia, and swims off as a new construct. An evolutionary search found a C-shapeda C-shaped parent, widely described in coverage as AI-designed, that gathers cells more efficientlyparent, widely described in coverage as AI-designed, that gathers cells more efficiently than athan a sphere and sustains the cycle for more rounds.sphere and sustains the cycle for more rounds. Nothing is copied. No genome is read or written, no template is used, and the offspring areNo genome is read or written and no template is used. The offspring are spheroids that do notspheroids that do not inherit the parent's shape, so the very feature that made a good replicator isinherit the parent's shape, so the feature that made the parent a good replicator is lost in thelost in the first generation. The dish must be restocked with fresh cells by an experimenter; takefirst generation. An experimenter has to keep restocking the dish with fresh cells, and without thatthat away and the process stops immediately. This is replication in von Neumann's kinematic sense —supply the process stops immediately. This is replication in von Neumann's kinematic sense, theassembly of a copy from parts already present — rather than in the biological sense of heredity withassembly of a copy from parts already present, rather than in the biological sense of heredity withvariation.[^vonneumann1966]variation.[^vonneumann1966] > [!caution] Not replication in the biological sense> [!caution] Not replication in the biological sense> Constructs that genuinely propagate a design through a population, such as a [[gene-drive]], do it> Constructs that genuinely propagate a design through a population, such as a [[gene-drive]], do it> by copying DNA — the mechanism absent here. Without heredity there is no variation for selection to> by copying DNA, which is the mechanism missing here. Without heredity there is no variation for> act on, so the process cannot evolve, and the runaway scenarios of the [[grey-goo]] literature> selection to act on, so the process cannot evolve. The runaway scenarios of the [[grey-goo]]> require a closure over materials and energy that nothing in this work approaches.> literature also require a closure over materials and energy that nothing in this work approaches. ## Anthrobots and human cells## Anthrobots and human cells The same laboratory has reported an equivalent construct made from adult human cells. AnthrobotsThe same laboratory has reported an equivalent construct made from adult human cells. Anthrobotsself-assemble from donated tracheal epithelial cells, which under the right culture conditions turnself-assemble from donated tracheal epithelial cells, which under the right culture conditions turntheir cilia outward and become motile spheroids ranging from tens to a few hundred micrometrestheir cilia outward and become motile spheroids ranging from tens to a few hundred micrometresacross.[^gumuskaya2023] They are made without reprogramming, unlike constructs built onacross.[^gumuskaya2023] Unlike constructs built on [[induced-pluripotent-stem-cells]], they are made[[induced-pluripotent-stem-cells]], and without an external scaffold, unlike [[organ-bioprinting]]without reprogramming, and unlike [[organ-bioprinting]] or [[decellularized-scaffolds]], without anor [[decellularized-scaffolds]]. Nothing is imposed on the cells except the medium they sit in.external scaffold. The only thing imposed on the cells is the medium they sit in. In the reported experiment, clusters of anthrobots placed across a scratch in a monolayer ofIn the reported experiment, clusters of anthrobots were placed across a scratch in a monolayer ofcultured human neurons were followed by regrowth across the gap that untreated controls did notcultured human neurons, and regrowth followed across the gap in a way that untreated controls didshow. That is a result in a dish. No mechanism has been established and no animal has been treated,not show. That is a result in a dish. No mechanism has been established and no animal has beenand the distance between closing a scratch in culture and repairing tissue in a person is the onetreated. The step from closing a scratch in culture to repairing tissue in a person is one that mostmost of regenerative medicine has never crossed.of regenerative medicine has never managed. ## The morphogenesis claim## The morphogenesis claim The scientifically interesting argument attached to this work is not about robotics at all. LevinThe scientifically interesting argument attached to this work concerns development rather thanholds that the genome specifies cellular hardware rather than anatomy directly, that cells androbotics. Levin holds that the genome specifies cellular hardware rather than anatomy directly, thattissues coordinate through bioelectric signalling toward target morphologies, and that a group ofcells and tissues coordinate through bioelectric signalling toward target morphologies, and that acells removed from the signalling context of an embryo will settle into a different but stable bodygroup of cells removed from the signalling context of an embryo will settle into a different butplan.[^levin2021] On that reading a xenobot is not a machine made of tissue but a frog cellstable body plan.[^levin2021] On that reading a xenobot is a frog cell collective exercising ancollective exercising an option its genome always contained. Levin and Daniel Dennett have pressed aoption its genome always contained, rather than a machine made of tissue. Levin and Daniel Dennettstronger version of the framing, in which goal-directedness is a property found at every scale ofhave pressed a stronger version of the framing, in which goal-directedness is a property found atbiology rather than only in nervous systems.[^dennett2020] Supporting work outside the xenobotevery scale of biology rather than only in nervous systems.[^dennett2020]programme comes from planarian flatworms: after a brief disruption of gap-junction signalling aminority regenerate two heads, and those animals go on yielding two-headed worms through lateramputations in plain water, with no change to their DNA.[^durant2017] The result bears on[[limb-regeneration]] and on what a genome does and does not determine. Supporting work outside the xenobot programme comes from planarian flatworms. After a briefdisruption of gap-junction signalling a minority regenerate two heads, and those animals go onyielding two-headed worms through later amputations in plain water, with no change to theirDNA.[^durant2017] The result bears on [[limb-regeneration]] and on what a genome does and does notdetermine. > [!debate] How much does the construct actually show> [!debate] How much does the construct actually show> Critics accept the observations and dispute the interpretation. Dissociated amphibian cells were> Critics accept the observations and dispute the interpretation. Dissociated amphibian cells were> known to reaggregate and sort by tissue type in the 1950s, and ciliated epithelium swims because> known to reaggregate and sort by tissue type in the 1950s, and ciliated epithelium swims because> that is what ciliated epithelium does.[^townes1955] On the sceptical reading, a xenobot is a motile> that is what ciliated epithelium does.[^townes1955] On the sceptical reading, a xenobot is a> explant with a haircut, and the language of body plans, goals and reconfigurable organisms is> motile explant with a haircut, and the language of body plans, goals and reconfigurable organisms> doing work the data do not require. The reply from Levin's side is that a stable, reproducible,> is doing work the data do not require. Levin's side replies that a stable, reproducible,> functional morphology absent from the frog's life cycle is precisely what needs explaining. The> functional morphology absent from the frog's life cycle is exactly what needs explaining. The two> disagreement is about the explanatory frame, not the images.> camps disagree about the explanatory frame; neither disputes the images. ## Limitations## Limitations Two misreadings are near-universal in coverage. These are sub-millimetre objects, orders ofCoverage repeats two misreadings almost without exception. The first concerns scale. These aremagnitude larger than the constructions in the [[medical-nanorobots]] tradition and comparable tosub-millimetre objects, orders of magnitude larger than the constructions in thethe larger devices in [[microrobots-in-medicine]]; and they are not machines, containing no sensor,[[medical-nanorobots]] tradition and comparable to the larger devices inno actuator, no controller, and no program. The evolutionary search runs on a computer before any[[microrobots-in-medicine]]. The second is that they are machines. They contain no sensor, actuator,cells are touched, and the resulting object cannot be reprogrammed, updated, or told what to do.controller or program. The evolutionary search runs on a computer before any cells are touched, andthe resulting object cannot be reprogrammed, updated, or told what to do. The transfer from simulation to tissue is loose. The simulator treats cells as voxels of passive orThe transfer from simulation to tissue is loose. The simulator treats cells as voxels of passive orcontractile material, omitting adhesion, signalling, and the tendency of tissue to remodel itself,contractile material and omits adhesion, signalling, and the tendency of tissue to remodel itself,so built constructs approximate their designs rather than instantiate them. Batch variation isso built constructs approximate their designs rather than instantiate them. Batch variation issubstantial, in the manner familiar from [[organoids]], and nothing can be steered: motion issubstantial, as it is with [[organoids]], and nothing can be steered: a shape biases where a swimmerdirected only in the statistical sense that a shape biases where a swimmer tends to go.tends to go, so motion is directed only in a statistical sense. No therapeutic application exists. Proposals in circulation — clearing microplastics from water,No therapeutic application exists. The proposals in circulation, such as clearing microplastics fromscraping plaque from vessels, carrying a payload in the manner of [[targeted-drug-delivery]] — arewater, scraping plaque from vessels, or carrying a payload in the manner ofspeculative in the strict sense that none has been attempted in an animal. A construct that runs out[[targeted-drug-delivery]], are speculative in the strict sense that none has been attempted in anof fuel in days, cannot be located once released, and consists of foreign frog cells has no obviousanimal. A construct that runs out of fuel in days, cannot be located once released, and consists ofroute into a body.foreign frog cells has no obvious route into a body. ## Risk and governance## Risk and governance The mainstream assessment of biosafety risk is that it is low, for a specific reason rather than aThe mainstream assessment is that the biosafety risk is low, and it rests on specific propertiesreassuring one: xenobots cannot feed themselves, cannot reproduce without cells supplied to them,rather than general reassurance. Xenobots cannot feed themselves, cannot reproduce without cellsand are built from vertebrate cells that die outside a controlled medium. That places them below thesupplied to them, and are built from vertebrate cells that die outside a controlled medium. Thatcontainment concerns motivating the safeguards in [[recoded-organisms]], and far below those aboutplaces them below the containment concerns behind the safeguards in [[recoded-organisms]], and far[[mirror-life]]. Invoking the [[precautionary-principle]] here is an argument about a researchbelow those about [[mirror-life]]. Invoking the [[precautionary-principle]] here amounts to anprogramme whose future forms cannot be specified, not about the constructs already made.argument about a research programme whose future forms cannot be specified; it says nothing aboutthe constructs already made. The harder questions are definitional. Whether these things are organisms, and what would be owed toThe harder questions are definitional. Whether these things are organisms, and what would be owed tothem if they were, meets the same absence of an agreed test that troublesthem if they were, runs into the same lack of an agreed test that troubles[[machine-consciousness]] — with less urgency than for cerebral organoids, since a xenobot contains[[machine-consciousness]], though with less urgency than for cerebral organoids, since a xenobotno neurons at all. Regulatory categories fit badly: a construct of unmodified animal cells is not acontains no neurons at all. Regulatory categories fit badly. A construct of unmodified animal cellsgenetically modified organism, not a medical device, and not a laboratory animal, the same gapis not a genetically modified organism, a medical device or a laboratory animal, the same gap that[[synthetic-embryos]] have opened from the other direction. The technique is also cheap and needs no[[synthetic-embryos]] have opened from the other direction. The technique is also cheap and needs nogene synthesis, so it sits outside most of the machinery built for [[dual-use-research]].gene synthesis, so it sits outside most of the machinery built for [[dual-use-research]]. ## Outlook## Outlook The near-term value of the work is as an experimental system rather than a product. It offers a wayIn the near term the work is worth more as an experimental system than as a product. It offers a wayto ask what a group of cells builds when the embryo's instructions are removed, on a timescale ofto ask what a group of cells builds when the embryo's instructions are removed, on a timescale ofdays and at a cost that permits many replicates, a question upstream of [[tissue-engineering]] anddays and at a cost that permits many replicates. That question sits upstream ofof every attempt at [[lab-grown-organs]]. Whether the constructs themselves ever do useful work is a[[tissue-engineering]] and of every attempt at [[lab-grown-organs]]. Whether the constructsseparate and longer bet: the missing pieces are a food supply, control, and a reason to prefer athemselves ever do useful work is a separate and longer bet, which would need a food supply, a meansliving object to an engineered one.of control, and a reason to prefer a living object to an engineered one. The claim that would matter most if it held is the one hardest to test. If anatomy is aThe claim that would matter most if it held is also the hardest to test. If anatomy is areconfigurable target rather than a fixed genomic output, then instructing cells at the level ofreconfigurable target rather than a fixed genomic output, then instructing cells at the level ofpattern, instead of editing the genes beneath it, becomes a legitimate strategy for regeneration.pattern, instead of editing the genes beneath it, becomes a legitimate strategy for regeneration.Frog cells arranged into something the frog never makes demonstrate that the option exists. They areFrog cells arranged into something the frog never makes show that the option exists. They do not yetnot yet evidence that anyone knows how to specify which option is taken.show that anyone knows how to specify which option is taken. ## See also## See also removed, struck through added, underlinedLine numbers count the serialised markdown of each revision, frontmatter included.
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