The Morphological, Behavioral, and Transcriptomic Life Cycle of Anthrobots
Fascinating aspects of morphogenetic and behavioral plasticity of living material are revealed by novel constructs that self‐construct from genetically wild‐type cells. Anthrobots arise from cultured adult human airway epithelial cells, developing, becoming self‐motile, and acquiring neural repair capabilities without exogenous genetic circuits or inorganic scaffolds. Progress in bioengineering and regenerative medicine depends on developing a predictive understanding of collective cell behavior in novel circumstances. Toward that end, here a number of life cycle properties of Anthrobots, including their morphogenesis, maturation, and demise, are quantitatively characterized. A self‐healing capacity and a remarkable reduction of epigenetic age upon morphogenesis are uncovered. Transcriptomic analysis reveals that assembling into Anthrobots drives a massive remodeling of gene expression relative to their cellular source, including several embryonic patterning genes, and a shift toward more evolutionarily ancient gene expression. These data reveal new aspects of engineered multicellular configurations, in which wild‐type adult human cells self‐assemble into an active living construct with its own distinct transcriptome, morphogenesis, and life history.
Biobots have significant potential to impact discovery in biology, biomedical engineering, and biomedicine, emerging as a unique blend of biological and robotic concepts. Their relevance broadly falls across 3 categories. First, they contribute to basic evolutionary, cell, and developmental biology by revealing the developmental plasticity of cellular and tissue‐level morphogenesis in novel contexts, which are not apparent from stereotypical wild‐type development. Second, they can be used as a sandbox for bioengineering, active matter, and synthetic morphology efforts to understand the rules of self‐assembly of living materials for creation of novel synthetic living machines.[ 1 ] Finally, they show promise as a technology for sensing and delivery of stimuli and cargo in vivo, in biomedical settings.[ 2 ]
Biobots can be categorized into three types: noncellular biobots, hybrid biobots, and fully cellular biobots.[ 3 ] Noncellular biobots are entirely robotic but inspired by biological forms or behaviors. Examples include Wehner et al.’s fully autonomous soft “octobot,”[ 4 ] Ze et al.’s origami millibots,[ 5 ] Dillinger et al.’s micrometer‐scale ciliary biobots,[ 6 ] Miskin et al.’s electromicroscopic robots,[ 7 ] and several others[ 7 , 8 ] that can be controlled via magnetic, ultrasonic, or electrochemical actuation. A prime feature of noncellular biobots is their reductionist design approach, which seeks full control over structure and behavior. Hybrid biobots, a combination of biological and inanimate components,[ 9 ] are exemplified by Nawroth et al.’s 2012 tissue‐engineered jellyfish[ 10 ] as well as Park et al.’s 2016 biohybrid ray.[ 11 ] These and other following examples of biobots[ 7 , 9 , 10 , 11 , 12 ] integrate specialized tissues (e.g., muscle) with inert scaffolds, e.g., Polydimethylsiloxane (PDMS) gels, leveraging this synergy to drive form and function. By contrast, fully cellular biobots do not use inanimate material to shape and support the structure and resulting function, instead relying solely on the inherent capacity of biological cells to autonomously adopt new forms and functions, such as self‐motility. The first examples of these fully cellular biobots were Blackiston et al.’s different types of Xenobots,[ 13 ] self‐motile ciliated spheroids derived from frog embryo cells. These bots were followed by Gumuskaya et al.’s first fully cellular human‐derived nonembryonic biobots in 2023, dubbed “Anthrobots.”[ 3 ]
Anthrobots are self‐constructing fully cellular biobots derived from human tracheal epithelia by reprogramming the development of an airway organoid. Airway organoids are 3D structures grown in vitro that mimic the architecture and function of the human airway.[ 14 ] These organoids can derive from multiple sources, including stem cells, normal human bronchial epithelial cells (NHBEs), and human donors. Airway organoids are commonly characterized by their ability to replicate the cellular diversity of the airway epithelium, including ciliated cells, goblet cells, and basal cells. They exhibit key functional properties of the airway, such as mucus production, ciliary beating, and response to external stimuli, making them accurate models for studying respiratory physiology and pathophysiology—or, in our case, ciliated synthetic biological constructs. The main difference between Anthrobots and airway organoids is that while the primary goal of the organoids is to recapitulate the native tissue architecture and physiology, Anthrobots and other biobots demonstrate new living form and function that is not explored by evolution but is useful for engineering purposes. They are used not only to make useful synthetic living machines but also to explore motility‐enabled behavior that reveals plasticity and emergent features not apparent in organoid assays but may be of relevance to studies of evolution of behavior in basal forms of life and the emerging field of diverse (nonneural) intelligence.[ 15 ]
During maturation, various environmental cues can guide airway organoids toward certain morphologies, of which one of the most relevant is the topology of the cell's apicobasal polarity; this is important because active structures known as cilia form on the cells’ apical surface, and these can be oriented toward the inside of the sphere or the outside. By maintaining cell aggregates in growth media and Matrigel, airway organoids will develop a membrane with its apical (ciliated) surface facing inward. However, an apical‐out phenotype has recently been shown, resulting in cilia covering the exterior of the organoids. This phenotype has been accomplished using a variety of techniques, including air–liquid interfaces (ALI) with cells embedded in collagen,[ 16 ] microwells that mold individual cell aggregates,[ 17 ] U‐bottom wells without any extracellular matrix present,[ 18 ] as well as in the case of Anthrobots, by way of sudden environmental phase shift from a semisolid to a liquid state.[ 3 ] All these different approaches can trigger bronchial epithelium samples from humans to spontaneously form ciliated spheroids with self‐motility.
Anthrobots acquire shapes and behaviors quite different from any stage of human development or organogenesis; thus, they represent a fascinating opportunity to study the form and function of a new living configuration that had never been the subject of evolutionary selection in this form factor. Learning to predict and exploit emergent functionality of cellular materials is of critical importance to developing rational control in bioengineering and regenerative medicine contexts; Anthrobots are a new model system in which our nascent ability to predict novel life functions can be improved, specifically using an adult human cell source to study how much of the plasticity remains and can be functionally recovered in nonembryonic, complex life forms. Such synthetic examples of life are also interesting model systems from the perspective of evolutionary developmental biology and exobiology, as they are a unique context in which to understand “life as it could be,” as they differ from any known naturally evolved organism. Finally, because their morphogenesis and behavior are emergent in the context of wild‐type human cells, and not under control of exogenous synthetic circuits, molecular reprogramming factors, or nanomaterials, they can teach us much about the plasticity of the molecular hardware encoded by the genome.
Past work[ 3 ] characterized Anthrobots’ shape, motility, and most strikingly, ability to induce repair in neural wounds in vitro. However, many aspects of their life history remained unknown, including the details of their formation process, the dynamics of their maturation and death, and their ability to respond to mechanical damage (regenerative capacity, as occurs in numerous organisms). While the bots come from adult (including elderly) donors, we wondered what their age was: could the process of morphogenesis reverse the clock? Epigenetic clock analysis[ 19 ] revealed a significant reduction of age in the bots compared to their cellular source.
We also sought to characterize their transcriptome. While others study airway organoids as a model of human in vivo biology, we pursued a complementary perspective: as a new type of creature navigating an environment for which it was not directly selected, what genes would it express? We found massive alterations in the transcriptome of Anthrobots compared to their cells of origin, notably the upregulation of evolutionarily ancient genes. This reveals unexpected ways in which emergent morphogenesis regulates gene expression, including the appearance of embryonic patterning genes despite the adult origin of the cells and lack of genomic editing or transgenes. Taken together, these data shed light onto the natural history, at the molecular, cellular, tissue, physiological, and behavioral levels, of this novel synthetic architecture.
We first wanted to learn more about Anthrobots' self‐construction process and specifically investigated whether this process unfolds through a single path or whether there are different ways for Anthrobots to self‐construct as embedded in Matrigel, which may shine light onto their emergent morphological and behavioral differences.[ 3 ] To this end, we collected microscopy images of 28 Anthrobots every 2 days to track their growth in Matrigel throughout a 14 days developmental process. We analyzed these time‐course data through three major metrics: number of cellular collisions (“merge_events”), final spheroid area (“fin_area”), and the average standard deviation of area across the entire growth process (“sd_area”), as shown in Figure 1A. When this 3D data cloud was clustered with the WardD2 unsupervised clustering algorithm, we observed the emergence of three statistically orthogonal (Figure 1B) groups, each representing an Anthrobot growth type, which we named as dormant, merger expander, and monoclonal expander. The dormant typology consists of progenitor cells that start out as individual cells and never proliferate and develop into a multicellular spheroid (Figure 1C,c‐1). The merger expanders consist of the spheroids that result from the merging of one or multiple spheroids, each expanding from single cells through cellular proliferation (Figure 1C,c‐2). Finally, the monoclonal expanders are multicellular spheroids that can be tracked to a single ancestral cell (Figure 1C,c‐3). These classes are statistically distinct (as determined by the unsupervised WardD2 algorithm, p < 0.01). Thus, we conclude that Anthrobots have three different developmental fates.
Anthrobots undergo morphogenesis into a unique functional form despite their completely wild‐type human genome. What genes do Anthrobots express, and how do they compare to those of their parent tissue (airway epithelium) or to human embryos? To understand the plasticity of cell groups in the absence of genomic editing, we next sought to characterize their transcriptome. We first performed RNA‐seq on progenitor cells and day 0 Anthrobots (Figure 2A), and computationally identified differentially expressed genes (DEGs) that were unique to Anthrobots. Biological replicates of the samples clustered tightly, but showed very clear separation between the source cells and Anthrobots (Figure 2B). Remarkably, plotting the transcripts with a strict cutoff (log2 FC > 4) for significance revealed massive remodeling of the transcriptome (Figure 2C). Out of 22 518 transcripts, 8992 showed significant up‐ or downregulation. Thus, becoming an Anthrobot has a major effect on the expressed genetic information.
Anthrobots self‐assemble, but they are made of adult, not embryonic, cells. Does this process involve any transcriptional programs normally driving embryonic development? We applied pathway analysis through the Gene Ontology (GO) database[ 20 ] and found that the “embryonic patterning” gene category was highly represented when Anthrobot DEGs were compared to transcriptomic data of a human morula. We found that 13.4% of the overexpressed genes in Day0 bots compared to progenitor cells are genes activated at the morula stage. In addition, we found an enrichment in “multicellular organism development” (p < 0.005). We conclude that the formation of Anthrobots involves the activation of some embryonic transcriptional programs.
While Anthrobots appear to be spherically symmetric, and their source cells originate from the endodermal lineage, the embryonic‐like transcriptional signature led us to ask whether they expressed any embryonic markers of axial patterning[ 21 ] and germ layer formation[ 22 ] (Figure 2D). We observed the differential expression of both endoderm‐driver genes like Forkhead Box A1 (FOXA1) and Forkhead Box A2 (FOXA2)[ 23 ] as well as mesoderm drivers such as Forkhead Box C1 (FOXC1)[ 24 ] and Bone Morphogenetic Protein 7 (BMP7)[ 25 ] in the earlier phase of the developmental process from progenitor cells to a 3D Anthrobot precursor spheroid. Key genes associated with ectoderm formation, such as Forkhead Box P2 (FOXP2),[ 26 ] were not yet upregulated. Furthermore, while BMP7,[ 25 ] which is also a marker of dorsal–ventral (DV) patterning, as well as the Homeobox Gene Expressed in ES Cells (HESX),[ 27 ] driver of anterior–posterior (AP) patterning, were seen to be upregulated in this stage, Sonic Hedgehog (SHH),[ 28 ] driver of left–right (LR) patterning, remained silenced. These findings indicate that Anthrobots, although not initiated from embryonic cells, demonstrate some molecular hallmarks of embryonic development as they display transcriptomic signatures that align with endoderm and mesoderm induction, as well as DV and AP patterning during this initial developmental stage, while the ectoderm genes, along with a LR patterning marker continuing to stay downregulated.
Next, we wondered whether the global transcriptomic changes associated with Anthrobot formation were associated with any phylogenetic shifts. To understand the age distribution of DEGs in Anthrobots under various conditions, we conducted a phylostratigraphic analysis[ 29 ] (see also Supplement S1 in the Supporting Information), which revealed important differences in the expression of ancient genes across conditions. We found that progenitor cells express 3812 and 1360 genes, respectively, in the evolutionary ages “All living organisms” and Eukaryota. For Day 0 and Day 10 bots, it is, respectively, 3987 and 1375, and 4004 and 1398 genes that are expressed in these two evolutionary ages. Thus, we observed an increase in the genetic expression for unicellular genes ranging from 175 to 209 genes in the category “All living organisms” age and from 15 to 38 in Eukaryota genes (see Figure 2E). In addition, we observed that this effect is even more pronounced when we analyzed the DEGs between the anthrobots and their progenitor cells. Indeed, in the “Day0 Bots versus Progenitor Cells” and “Day10 Bots versus Progenitor Cells” conditions, we observed, respectively, 429 and 602 overexpressed genes (logFC > 2) for “All living organisms” evolutionary age and 93 and 107 overexpressed genes (log fold change (FC) > 2) in the Eukaryota evolutionary age (see Figure 2F).
Thus, phylostratigraphic analysis reveals that in addition to their transcriptome becoming more similar to that of embryos (moving backward in an ontogenetic sense), they also shift toward more ancient gene expression (moving backward in a phylogenetic sense).
Anthrobots undergo eversion as they mature, which brings the cilia into an outward‐facing orientation.[ 3 ] To better characterize this process (Figure 1A), we next investigated whether this process unfolds through a single behavioral pattern or whether there are different paths for Anthrobots to undergo eversion upon their dissolution from Matrigel. We collected time‐lapse microscopy images from 27 Anthrobots during the first 48 h upon their dissolution from Matrigel with the goal of ascertaining its behavior over its entire trajectory. We analyzed these time course data (Figure 3A) through a principal components analysis (PCA) composed of 14 axes featuring major metrics: the mean, median, and standard deviation of the angular speed, linear distance, heading and linear speed, as well as the movement straightness and gyration. When this 3D data cloud was clustered using the WardD2 unsupervised clustering algorithm, we observed two statistically orthogonal (Figure 3B) groups, each representing a distinct Anthrobot behavior during the eversion process, which we called displacers and statics (Figure 3C). The main distinguishing factor between these two different modes of eversion is the fact that while one group (group#1: displacers) consists of bots that show some degree of motility during the eversion process (Figure 3D‐1), the other group (group #2: static bots) show no motility during this process (Figure 3D‐2). Displacement during eversion is a surprising behavior given Anthrobot motility is generated by ciliary activity, which only surfaces at the end of the eversion process.
This unexpected behavior, which may be due to some bots’ ability to displace mid‐eversion, thanks to partial localization of ciliated cells in the bot surface could grant Anthrobots with new capabilities, such as efficient engulfment of agents of interest in the environment, (e.g., particles, filament, or debris), as shown in Figure 3E.
Having characterized morphogenetic rearrangements in the maturing Anthrobots, we next sought to better understand the transcriptomic landscape of this synthetic self‐assembly process, as day 0 Anthrobots progress toward day 10 Anthrobots. RNA‐seq analysis (Figure 4A) revealed significant differences (Figure 4B) that show significant changes (Figure 4C) in the expression of FOXA1, FOXA2, Fibroblast Growth Factor 8 (FGF8), FOXP2, Homeobox Gene Expressed in ES Cells 1 (HESX1), SHH genes – a further remodeling of gene expression past the initial changes compared to their tissue of origin (Figure 2). We conclude that Anthrobots undergo a second massive transcriptomic rearrangement, during their maturation.
Although the Anthrobots are made of adult human donor cells, they undergo significant morphogenetic processes, which raised the question of whether they expressed any genes associated with embryonic development despite their advanced age. The genes we were especially interested in were those involved in germ layer specification and establishment of primary body axes (Figure 4D). In this middle stage of Anthrobot development from day 0 to day 10, we observed no considerable change in the expression of endoderm‐associated genes such as FOXA1 and FOXA2, as well as a downregulation of mesoderm‐driver genes such as FOXC1,[ 24 ] BMP7.[ 25 ] We did, however, find upregulation of the key genes associated with ectoderm such as FOXP2 [ 26 ] in day 10 bots. Furthermore, HESX11,[ 27 ] a gene involved in anterior–posterior differentiation, becomes further upregulated in day 10 Anthrobots as well. Likewise, a key regulator of left–right patterning and neurogenesis – SHH [ 28 ] – which had been silent throughout earlier stages of Anthrobot formation, also gets upregulated at this later stage. Taken together, these findings indicate that Anthrobots, although not initiated from embryonic cells, demonstrate molecular hallmarks of embryonic development as they mature, including transcriptomic signatures associated with the mesoderm to ectoderm transition, as well as anterior–posterior and left–right patterning.
Having characterized the morphological and transcriptomic changes in developing and maturing Anthrobot populations, we next sought to characterize their aging profile. We collected weekly motility data from an arbitrarily chosen subset of Anthrobots to better understand behavioral profiles over time. The weekly counts of baseline behavioral activity, defined as any cilia‐induced movement, exhibited consistent levels (Figure 5A) despite the declining population. Anthrobots approaching weeks 4–8 in their life cycle experience visible structural degradation (Figure 5B; refer to Figure 6 for a more comprehensive analysis). However, the frequency of motile behavior among intact bots at any given time remains steady, indicating bots do not cease their movement as they age, but only stop when they die – we found no evidence of an increasing elderly, fully immobile phase of life.
These living constructs underwent spontaneous morphogenesis and massive transcriptional remodeling with some embryonic signatures but were made of adult patients’ cells. What is their actual age? We decided to use human methylation aging clocks[ 19 ] to better understand the impact of the Anthrobot life cycle on the age of the cells comprising them (Figure 5C). The experiment involved the use of cells from a 21 years old donor to create two sets of Anthrobots, aged 10 and 25 days, respectively. Methylation clock analysis was conducted to determine the tissue age of passage 1 primary cells, yielding a calculated tissue age of 25 years based on mean values. Remarkably, comparative analysis against the donor's recorded age and that of the cells revealed a substantial reversal in the methylation clock upon differentiation into Anthrobots. Specifically, the 10 days old Anthrobots displayed a mean age of 18.7 years, while the 25 days old Anthrobots exhibited a mean age of 20 years. These results suggest that the Anthrobots underwent a reversal in biological age – the process of development into bots reduced their epigenetic age by 25%.
Finally, we asked whether Anthrobots had the capacity to repair after damage, and if so, given that this was not a normal human target morphology for any endogenous tissue or organ, what shape would they repair to? In order to test morphogenetic robustness, we damaged Anthrobots with a hypodermic needle and collected time‐lapse videos to characterize the response (Figure 5D and Video S1 (Supporting Information)). We observed that within the first 10–20 min of damage, the Anthrobots flex, and slowly return to the original shape they were in prior to the damage. The majority of structural recovery is owed to this immediate attempt to return to the original shape. Following this immediate damage recovery, we continued imaging the damaged bots through long‐term time‐lapse over the course of 48–72 h and observed no further “healing” or return to original shape beyond what they had recovered in the first 20 min. Furthermore, we observed that Anthrobots separated into two halves by the needle do not return to a single shape by the end of the 72 h; they remain distinct bodies. However, the initial flexing is present in the first 20 min postdamage.
Out of the 23 Anthrobots that were time‐lapsed immediately after being damaged, 16 showed recovery to their original spheroid shape, and 6 remained at an intermediate state (not fully indistinguishable from their original shape). One Anthrobot clearly did not show any recovery. Anthrobots showed no further recovery during a longer 72 h time‐lapse, and if they suffered a separation or a split during this period, they did not reform into a single whole but stayed in distinct pieces.
Anthrobots begin to degrade as they age, shrinking in size and losing displacement ability.[ 3 ] To better characterize Anthrobot aging and degradation, we next investigated whether this process unfolds through a single behavioral pattern or whether there are different paths for Anthrobots to degrade. We collected time‐lapse microscopy images from 36 Anthrobots during the first 35 days upon their dissolution from Matrigel with the goal of characterizing their degradation rate. We analyzed these time course data (Figure 6A) through a PCA analysis composed of 8 major metrics: Initial area (area of bot in 1st frame), fin area (area of bot in final trackable frame), change in area (difference between fin area and initial area), percent change (change in area/initial area × 100), standard deviation of difference in areas (SD of change in area between successive frames), mean of difference in areas (mean of change in area between successive frames), time to disintegrate (number of frames until the bot becomes untrackable), and changerate (the maximum difference in the difference of areas, akin to the second derivative for the area). When this 3D data cloud was clustered using the WardD2 unsupervised clustering algorithm, we observed two statistically orthogonal (Figure 6B) groups, revealing a positive correlation between bots’ initial morphology and their life span. Regardless of initial morphology, all Anthrobots are subject to a similar rate of degradation, resulting in large bots living longer than smaller Anthrobots (Figure 6C). This reveals that Anthrobot initial morphology has a significant impact on Anthrobot longevity, as opposed to there being a definite life span across the entire population.
Here, we focused on investigating the morphological, behavioral, and transcriptomic life stages of Anthrobots. We started by examining the self‐construction process of Anthrobots: as they mature, Anthrobots undergo eversion, bringing the cilia into an outward‐facing orientation. We found three distinct paths by which Anthrobots can self‐construct when embedded in Matrigel, illustrating a degree of variability/individuality in their morphogenesis. We also found that Anthrobots can recover their functional form after drastic mechanical injury (consistent with data in spheroids made from neonatal keratinocytes[ 30 ]). The fact that they self‐repair is likely an emergent feature of generic epithelial dynamics,[ 31 ] because Anthrobots were never part of an evolutionary process in which ability to repair themselves was selected for, which impacts our understanding of the evolution of traits such as regeneration.[ 32 ] This self‐repair process could make them a useful model for screening healing interventions or investigating the differences in self‐repair from cells of donors of different ages.[ 33 ] Moreover, it has relevance to studies of mechanisms of epithelial closure,[ 34 ] and also bodes well for the use of such biobots in vitro or in bioengineering settings, as they would not only be somewhat robust to damage from their environment, but could also positively affect nearby tissues via any secreted molecules that promote their own healing (as shown previously in their effects on neural scratch wounds[ 3 ]).
A key question in evolutionary developmental biology concerns the relationship between the molecular‐genetic and morphobehavioral information, and possible bidirectional control loops between them. Given that gene expression is under strong selection forces by a history in a specific environment, what would the transcriptome of a motile, self‐assembling novel living construct look like? We explored the genes expressed by Anthrobots and compared them to those of their parent tissue (airway epithelium) or human embryos to understand the plasticity of cell groups in the absence of genomic editing. We found that Anthrobots exhibit a much‐altered transcriptome and display embryonic markers, especially genes involved in axial patterning (consistent with other studies in the field, including nonhuman and salivary gland models[ 35 ]). Future studies using spatial transcriptomics will be needed to determine whether cryptic tissue‐level polarity or other kinds of biochemical patterning exist in the Anthrobots. More broadly, numerous kinds of synthetic constructs, such as more conventional scaffold‐based biobots,[ 1 , 12 , 36 ] should be examined via mRNA‐ and protein‐level omics approaches to look for novel gene expression profiles induced by morphological configuration and behavior alone.
To understand the life cycle of this novel synthetic construct, we collected weekly motility data and behavioral profiles of aging Anthrobots; they displayed robust behavioral longevity, remaining motile until the very end of their lifespan, at which point they degrade by spontaneously dissociating. We investigated the aging and degradation of Anthrobots, finding that regardless of their initial size, Anthrobots degrade at a steady rate, resulting in larger bots living longer. Information on their end of life is important for potential in vivo uses of Anthrobots in patients for proregenerative applications.[ 37 ] We also believe in vitro Anthrobots provide an attractive platform for screening antiaging candidate interventions, because they can be made patient‐specific, and because unlike traditional cell culture and organoid models, they offer motility, which can be used to quantify effects of putative prolongevity reagents not only on anatomical and molecular markers, but on active behavior. Ongoing studies will characterize that behavior with respect to ability to follow gradients (preferences) and ability to learn in simple assays.[ 15 , 38 ]
The Anthrobots have a somewhat unique life history because the age of their cells does not match the age of their anatomical structure: they are made of adult (even elderly) cells, but their life as a multicellular creature begins anew. Anthrobots and similar systems stand to impact the field of longevity,[ 39 ] as they reveal scenarios beyond the meiosis of embryogenesis that provide the reset needed to reverse aging.[ 40 ] Thus, we sought to understand what impact their new morphogenetic configuration might have on cell‐level markers of aging, via an epigenetic clock approach;[ 41 ] molecular clocks (and especially epigenetic clocks) have proven to be a valuable window on the aging process.[ 41 , 42 ] We found that fully assembled and motile multicellular Anthrobots are younger than their cells of origin. This is notable because it did not require any of the expected rejuvenation treatment and occurred in the absence of up‐regulation (forced or natural) of the Yamanaka reprogramming factors. What might have caused it? A similar event has been found in embryos,[ 43 ] and it has been seen that senescence can be reduced by 3D culture.[ 44 ]
Our data with adult‐derived cells reveal that reduction of epigenetic age may not be an exclusive, programmed feature of embryonic development but could be generically induced by morphogenetic processes. One way to think about this is from the perspective of the cells as information‐processing agents which integrate signals from their internal and external environment. On the one hand, these cells had molecular components consistent with decades of adult life. On the other hand, all their current evidence – transcription of embryonic axial patterning genes, mechanical stresses of morphogenesis, etc., points to being part of an embryo. In the current protocol, this conflicting information induces a moderate roll‐back of the epigenetic clock (consistent with data[ 45 ] on substrates that can return pluripotent stem cells to a naïve state). Our data are consistent with psychogenic contributions to aging,[ 40b ] in the sense that the physiological, morphological, and behavioral inputs during self‐assembly into a coherent 3D structure provide a kind of “age evidencing” that can propagate to other cellular age endpoints. To enhance this effect, with possible implications for the field of longevity, we suggest a research roadmap that exploits recent advances in extending neural decision‐making dynamics to understand cell responses.[ 46 ] Frameworks such as active inference could be used to guide interventions to cell signaling[ 47 ] to modify cells’ internal model of their own age.
There were a number of limitations in this study. Still unknown are metabolic profiles and consequences of this self‐assembly process. Likewise, the factors responsible for the individuality of the bots (the variety of their behaviors, life span, etc.) are unknown. With respect to behavior, at this point we do not know the rules governing their motion, but experiments in enriched environments with living and nonliving features will help to probe their behavioral repertoire and thus expand our understanding of basal cognition (especially in evolutionarily novel forms), and provide additional endpoints for screening of antiaging and nootropic compounds. Future work will also characterize Anthrobots’ biomechanical and bioelectrical properties, and the use of stimuli during their self‐construction process to guide form and function.
Synthetic living constructs made of the patient's own cells have the potential to impact biomedicine and in vitro organ bioengineering. Especially important is to augment studies of native biology in organoid models with ones that examine the emergent motile behaviors and nascent life histories, so that their properties and competencies can be predicted, exploited, and shaped toward useful applications. This technology is a positive contribution to active discussions of ethics in bioengineering and organoid research[ 48 ] because they do not need to include brain tissue, are not derived from embryos, can be made from the patient's own cells with no heterologous animal material or nanomaterial components, and have a limited lifespan. This avoids some thorny issues that affect other related technologies.