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1.
Bioinspir Biomim ; 19(3)2024 Apr 03.
Article de Anglais | MEDLINE | ID: mdl-38467068

RÉSUMÉ

Bioinspired and biomimetic soft grippers are rapidly growing fields. They represent an advancement in soft robotics as they emulate the adaptability and flexibility of biological end effectors. A prominent example of a gripping mechanism found in nature is the octopus tentacle, enabling the animal to attach to rough and irregular surfaces. Inspired by the structure and morphology of the tentacles, this study introduces a novel design, fabrication, and characterization method of dielectric elastomer suction cups. To grasp objects, the developed suction cups perform out-of-plane deflections as the suction mechanism. Their attachment mechanism resembles that of their biological counterparts, as they do not require a pre-stretch over a rigid frame or any external hydraulic or pneumatic support to form and hold the dome structure of the suction cups. The realized artificial suction cups demonstrate the capability of generating a negative pressure up to 1.3 kPa in air and grasping and lifting objects with a maximum 58 g weight under an actuation voltage of 6 kV. They also have sensing capabilities to determine whether the grasping was successful without the need of lifting the objects.


Sujet(s)
Octopodiformes , Robotique , Animaux , Biomimétique/méthodes , Élastomères , Octopodiformes/anatomie et histologie , Robotique/méthodes
3.
Brain Struct Funct ; 228(5): 1283-1294, 2023 Jun.
Article de Anglais | MEDLINE | ID: mdl-37138199

RÉSUMÉ

Coleoid cephalopods have a high intelligence, complex structures, and large brain. The cephalopod brain is divided into supraesophageal mass, subesophageal mass and optic lobe. Although much is known about the structural organization and connections of various lobes of octopus brain, there are few studies on the brain of cephalopod at the molecular level. In this study, we demonstrated the structure of an adult Octopus minor brain by histomorphological analyses. Through visualization of neuronal and proliferation markers, we found that adult neurogenesis occurred in the vL and posterior svL. We also obtained specific 1015 genes by transcriptome of O. minor brain and selected OLFM3, NPY, GnRH, and GDF8 genes. The expression of genes in the central brain showed the possibility of using NPY and GDF8 as molecular marker of compartmentation in the central brain. This study will provide useful information for establishing a molecular atlas of cephalopod brain.


Sujet(s)
Octopodiformes , Animaux , Octopodiformes/génétique , Octopodiformes/anatomie et histologie , Octopodiformes/métabolisme , Encéphale/métabolisme , Neurones/métabolisme , Analyse de profil d'expression de gènes , Transcriptome
4.
Curr Biol ; 32(1): 97-110.e4, 2022 01 10.
Article de Anglais | MEDLINE | ID: mdl-34798049

RÉSUMÉ

Octopods are masters of camouflage and solve complex tasks, and their cognitive ability is said to approach that of some small mammals. Despite intense interest and some research progress, much of our knowledge of octopus neuroanatomy and its links to behavior and ecology comes from one coastal species, the European common octopus, Octopus vulgaris. Octopod species are found in habitats including complex coral reefs and the relatively featureless mid-water. There they encounter different selection pressures, may be nocturnal or diurnal, and are mostly solitary or partially social. How these different ecologies and behavioral differences influence the octopus central nervous system (CNS) remains largely unknown. Here we present a phylogenetically informed comparison between diurnal and nocturnal coastal and a deep-sea species using brain imaging techniques. This study shows that characteristic neuroanatomical changes are linked to their habits and habitats. Enlargement and division of the optic lobe as well as structural foldings and complexity in the underlying CNS are linked to behavioral adaptation (diurnal versus nocturnal; social versus solitary) and ecological niche (reef versus deep sea), but phylogeny may play a part also. The difference between solitary and social life is mirrored within the brain including the formation of multiple compartments (gyri) in the vertical lobe, which is likened to the vertebrate cortex. These findings continue the case for convergence between cephalopod and vertebrate brain structure and function. Notably, within the current push toward comparisons of cognitive abilities, often with unashamed anthropomorphism at their root, these findings provide a firm grounding from which to work.


Sujet(s)
Octopodiformes , Animaux , Encéphale/anatomie et histologie , Cognition , Écosystème , Mammifères , Octopodiformes/anatomie et histologie , Perception visuelle
5.
Elife ; 102021 08 24.
Article de Anglais | MEDLINE | ID: mdl-34425939

RÉSUMÉ

Cephalopods have evolved nervous systems that parallel the complexity of mammalian brains in terms of neuronal numbers and richness in behavioral output. How the cephalopod brain develops has only been described at the morphological level, and it remains unclear where the progenitor cells are located and what molecular factors drive neurogenesis. Using histological techniques, we located dividing cells, neural progenitors and postmitotic neurons in Octopus vulgaris embryos. Our results indicate that an important pool of progenitors, expressing the conserved bHLH transcription factors achaete-scute or neurogenin, is located outside the central brain cords in the lateral lips adjacent to the eyes, suggesting that newly formed neurons migrate into the cords. Lineage-tracing experiments then showed that progenitors, depending on their location in the lateral lips, generate neurons for the different lobes, similar to the squid Doryteuthis pealeii. The finding that octopus newborn neurons migrate over long distances is reminiscent of vertebrate neurogenesis and suggests it might be a fundamental strategy for large brain development.


Octopuses have evolved incredibly large and complex nervous systems that allow them to perform impressive behaviors, like plan ahead, navigate and solve puzzles. The nervous system of the common octopus (also known as Octopus vulgaris) contains over half a billion nerves cells called neurons, similar to the number found in small primates. Two thirds of these cells reside in the octopuses' arms, while the rest make-up a central brain that sits between their eyes. Very little is known about how this central brain forms in the embryo, including where the cells originate and which molecular factors drive their maturation in to adult cells. To help answer these questions, Deryckere et al. studied the brain of Octopus vulgaris at different stages of early development using various cell staining and imaging techniques. The experiments identified an important pool of dividing cells which sit in an area outside the central brain called the 'lateral lips'. In these cells, genes known to play a role in neural development in other animals are active, indicating that the cells had not reached their final, mature state. In contrast, the central brain did not seem to contain any of these immature cells at the point when it was growing the most. To investigate this further, Deryckere et al. used fluorescent markers to track the progeny of the dividing cells during development. This revealed that cells in the lateral lips take on a specific neuronal fate before migrating to their target region in the central brain. Newly matured neurons have also been shown to travel large distances in the embryos of vertebrates, suggesting that this mechanism may be a common strategy for building large, complex brains. Although the nervous system of the common octopus is comparable to mammals, they evolved from a very distant branch of the tree of life; indeed, their last common ancestor was a worm-like animal that lived about 600 million years ago. Studying the brain of the common octopus, as done here, could therefore provide new insights into how complex nervous systems, including our own, evolved over time.


Sujet(s)
Migration animale , Encéphale/croissance et développement , Mouvement cellulaire , Cellules souches neurales/physiologie , Neurones/physiologie , Octopodiformes/anatomie et histologie , Octopodiformes/physiologie , Animaux , Animaux nouveau-nés , Facteurs de transcription à motif basique hélice-boucle-hélice/génétique , Encéphale/cytologie , Encéphale/physiologie
6.
Zoology (Jena) ; 147: 125940, 2021 08.
Article de Anglais | MEDLINE | ID: mdl-34198204

RÉSUMÉ

Octopuses have eight radially symmetrical arms that surround the base of a bilaterally symmetrical body. These numerous appendages, which explore the environment, handle food, and defend the animal against predators, are highly susceptible to truncation or loss. Here, we used scaling relationships specific to the arms of three sympatric octopus species of the genus Octopus, to calculate the proportion of arm truncation. We then compared the frequency and proportion of arm losses between different body locations. Truncated arms were found in 59.8 % of specimens examined, with individuals bearing one to as many as seven injured arms. We found a significant left side bias for greater proportion of arm truncation for all species and sexes except in O. bimaculatus males. We also found that sister species O. bimaculatus and O. bimaculoides had a greater proportion of their anterior arms (pairs 1 and 2) truncated, while in O. rubescens, posterior arms (pairs 3 and 4) were more truncated. The mean percent of arm that was truncated was 28.1 % overall but varied between species and by sex and was highest in O. rubescens females (56 %). The arms of O. rubescens also exhibited the steepest scaling patterns, and showed a positive correlation between body size and number of truncated arms. Overall, we show that arm injuries in our sampling of three intertidal species are frequent and asymmetrical, and that when injured, octopus on average lose a considerable proportion of their arm. Through quantifying the variation in arm truncation, this study provides a new foundation to explore behavioral compensation for arm loss in cephalopods.


Sujet(s)
Membres/traumatismes , Octopodiformes/anatomie et histologie , Animaux , Femelle , Mâle , Octopodiformes/classification , Spécificité d'espèce
7.
Vet Ophthalmol ; 24(3): 218-228, 2021 May.
Article de Anglais | MEDLINE | ID: mdl-33596337

RÉSUMÉ

PURPOSE: Review octopus ocular anatomy and describe the histopathologic findings in three octopuses diagnosed with phakitis and retinitis. ANIMALS: Two common octopuses (Octopus vulgaris) and one giant Pacific octopus (Enteroctopus dofleini) with a history of ophthalmic disease. METHODS: A literature search was performed for the ocular anatomy section. Both eyes from all three octopuses, and two control eyes, were submitted for histopathologic evaluation. Hematoxylin and eosin stain was used for standard histopathologic evaluation; GMS stain was used to screen for fungi, gram stain for bacteria; and Fite's acid fast stain for acid fast bacteria. RESULTS: Anatomically, the anterior chamber of the octopus has direct contact with ambient water due to an opening in the dorsal aspect of a pseudocornea. The octopus lens is divided into anterior and posterior segments. The anterior half is exposed to the environment through the opening into the anterior chamber. Neither part of the lens has a lens capsule. The retina is everted, unlike the inverted vertebrate retina, and consists of just two layers. Histopathology revealed inflammatory phakitis and retinitis of varying severity in all six eyes of the study animals. No intraocular infectious organisms were recognized but one common octopus eye had clusters of coccidian parasites, identified as Aggregata sp., in extraocular tissues and blood vessels. CONCLUSION: We describe inflammatory phakitis and retinitis in two species of octopuses. The underlying cause for the severe intraocular response may be direct intraocular infection, water quality, an ocular manifestation of a systemic disease, or natural senescence.


Sujet(s)
Octopodiformes/anatomie et histologie , Rétinite/médecine vétérinaire , Animaux , Techniques de diagnostic ophtalmologique/médecine vétérinaire , Femelle , Mâle , Rétinite/diagnostic
8.
Cell ; 183(3): 594-604.e14, 2020 10 29.
Article de Anglais | MEDLINE | ID: mdl-33125889

RÉSUMÉ

Animals display wide-ranging evolutionary adaptations based on their ecological niche. Octopuses explore the seafloor with their flexible arms using a specialized "taste by touch" system to locally sense and respond to prey-derived chemicals and movement. How the peripherally distributed octopus nervous system mediates relatively autonomous arm behavior is unknown. Here, we report that octopus arms use a family of cephalopod-specific chemotactile receptors (CRs) to detect poorly soluble natural products, thereby defining a form of contact-dependent, aquatic chemosensation. CRs form discrete ion channel complexes that mediate the detection of diverse stimuli and transduction of specific ionic signals. Furthermore, distinct chemo- and mechanosensory cells exhibit specific receptor expression and electrical activities to support peripheral information coding and complex chemotactile behaviors. These findings demonstrate that the peripherally distributed octopus nervous system is a key site for signal processing and highlight how molecular and anatomical features synergistically evolve to suit an animal's environmental context.


Sujet(s)
Cellules chimioréceptrices/métabolisme , Octopodiformes/physiologie , Toucher/physiologie , Acétylcholine/pharmacologie , Séquence d'acides aminés , Animaux , Comportement animal , Femelle , Cellules HEK293 , Humains , Octopodiformes/anatomie et histologie , Octopodiformes/génétique , Récepteurs de surface cellulaire/composition chimique , Récepteurs de surface cellulaire/métabolisme , Récepteurs cholinergiques/métabolisme , Transduction du signal
9.
Curr Biol ; 30(21): 4322-4327.e3, 2020 11 02.
Article de Anglais | MEDLINE | ID: mdl-32916119

RÉSUMÉ

Octopuses are active predators with highly flexible bodies and rich behavioral repertoires [1-3]. They display advanced cognitive abilities, and the size of their large nervous system rivals that of many mammals. However, only one third of the neurons constitute the CNS, while the rest are located in an elaborate PNS, including eight arms, each containing myriad sensory receptors of various modalities [2-4]. This led early workers to question the extent to which the CNS is privy to non-visual sensory input from the periphery and to suggest that it has limited capacity to finely control arm movement [3-5]. This conclusion seemed reasonable considering the size of the PNS and the results of early behavioral tests [3, 6-8]. We recently demonstrated that octopuses use visual information to control goal-directed complex single arm movements [9]. However, that study did not establish whether animals use information from the arm itself [9-12]. We here report on development of two-choice, single-arm mazes that test the ability of octopuses to perform operant learning tasks that mimic normal tactile exploration behavior and require the non-peripheral neural circuitry to use focal sensory information originating in single arms [1, 10]. We show that the CNS of the octopus uses peripheral information about arm motion as well as tactile input to accomplish learning tasks that entail directed control of movement. We conclude that although octopus arms have a great capacity to act independently, they are also subject to central control, allowing well-organized, purposeful behavior of the organism as a whole.


Sujet(s)
Comportement animal/physiologie , Système nerveux central/physiologie , Membres/physiologie , Mouvement/physiologie , Octopodiformes/physiologie , Animaux , Comportement d'exploration/physiologie , Membres/innervation , Apprentissage/physiologie , Octopodiformes/anatomie et histologie , Proprioception/physiologie , Perception du toucher/physiologie
10.
Sci Rep ; 10(1): 15480, 2020 09 23.
Article de Anglais | MEDLINE | ID: mdl-32968184

RÉSUMÉ

In medical robotics, micromanipulation becomes particularly challenging in the presence of blood and secretions. Nature offers many examples of adhesion strategies, which can be divided into two macro-categories: morphological adjustments and chemical adaptations. This paper analyzes how two successful specializations from different marine animals can converge into a single biomedical device usable in moist environments. Taking inspiration from the morphology of the octopus sucker and the chemistry of mussel secretions, we developed a protein-coated octopus-inspired micro-sucker device that retains in moist conditions about half of the adhesion it shows in dry environments. From a robotic perspective, this study emphasizes the advantages of taking inspiration from specialized natural solutions to optimize standard robotic designs.


Sujet(s)
Micromanipulation , Octopodiformes , Robotique , Adhésivité , Animaux , Matériaux biomimétiques , Micromanipulation/instrumentation , Micromanipulation/méthodes , Mytilus edulis , Octopodiformes/anatomie et histologie , Robotique/instrumentation , Robotique/méthodes , Eau
11.
Anat Histol Embryol ; 49(4): 502-510, 2020 Jul.
Article de Anglais | MEDLINE | ID: mdl-32198901

RÉSUMÉ

The development of the epidermis of octopus, Octopus vulgaris, throughout its life cycle was studied by conventional staining and histochemical techniques using lectins. The mantle, the arm and the two parts of the suckers: the infundibulum and the acetabulum were analysed independently. With the exception of the suckers, the general morphology of the epidermis does not vary from the first days post-hatching to adulthood. In general terms, histochemical techniques do not indicate changes in the composition of glycoconjugates of the epidermis main cells, epithelial and secretory cells. The epithelial cells of the mantle and arm show positivity for mannose (ConA+) in their apical portions, indicating the presence of n-glycoproteins that, among other things, provide lubrication to the surface of the body. In the suckers, the apical surface of the infundibulum contains sulphated glycosaminoglycans of the N-acetylglucosamine type that provide adhesive properties. In addition to observing three types of mucocytes, m1 and m2 are characteristic of the mantle and arm, and m3 is found in the suckers. The paralarva epidermis is characterised by the presence of Kölliker's organs whose exact function is unknown. In this study, the absence of staining with alcian blue/periodic acid-Schiff(AB/PAS) prevents the possibility of attributing a secretory function. Nevertheless, the linkage of three lectins (WGA, LEL and GSL-I) in the fascicle of the organ suggests the presence of proteoglycans rich in N-acetylglucosamine that would mainly have a structural role.


Sujet(s)
Étapes du cycle de vie , Mucus/physiologie , Octopodiformes/anatomie et histologie , Peau/anatomie et histologie , Animaux , Épiderme/anatomie et histologie , Épiderme/composition chimique , Épiderme/physiologie , Glycoconjugués/analyse , Histocytochimie/médecine vétérinaire , Lectines , Mucus/composition chimique , Octopodiformes/composition chimique , Octopodiformes/croissance et développement , Peau/composition chimique , Peau/croissance et développement
12.
Proc Inst Mech Eng H ; 233(12): 1250-1261, 2019 Dec.
Article de Anglais | MEDLINE | ID: mdl-31617793

RÉSUMÉ

The vacuum chuck is widely used in industrial and daily life. By observing the macroscopic and microscopic morphology of octopus sucker, it is found that the sucker surface has concave-convex continuous wave shape with large number of non-smooth morphologies. The sealing mechanism of octopus sucker is analyzed according to its surface morphology before and after adsorption, and the non-smooth morphology is found to greatly enhance the adsorption. Based on the bionics theory, the non-smooth surface morphology of octopus sucker is applied to improve the sucker adsorption. And the bionic suckers with three types of grooves are designed. According to the model of standard and bionic suckers, the sucker entities are obtained by the method of three-dimensional printing and casting. And the tensile tests of suckers are carried out. The stress of suckers is analyzed by finite element method, and the sealing mechanism is discussed. According to the test results, the bionic sucker has larger adsorption force. And the ring sucker possesses the best adsorption performance. Compared with the standard sucker, the maximum adsorption force of the bionic sucker is increased by 12.2% in the air and 25.2% underwater. The adsorption force of bionic sucker becomes larger with the increase in the groove number; when the groove number increases to a certain extent, the adsorption force becomes smaller. The deformation of non-smooth morphology during adsorption makes the bionic sucker have a larger contact area. That is the reason why the bionic sucker has good adsorption performance. The bionic design of sucker can provide a new method to improve its adsorption.


Sujet(s)
Biomimétique/instrumentation , Bionique , Phénomènes mécaniques , Octopodiformes/anatomie et histologie , Adsorption , Animaux , Phénomènes biomécaniques , Conception d'appareillage , Analyse des éléments finis , Impression tridimensionnelle , Contrainte mécanique , Propriétés de surface
13.
J Exp Biol ; 222(Pt 19)2019 10 09.
Article de Anglais | MEDLINE | ID: mdl-31527179

RÉSUMÉ

Spontaneous nerve regeneration in cephalopod molluscs occurs in a relative short time after injury, achieving functional recovery of lost capacity. In particular, transection of the pallial nerve in the common octopus (Octopus vulgaris) determines the loss and subsequent restoration of two functions fundamental for survival, i.e. breathing and skin patterning, the latter involved in communication between animals and concealment. The phenomena occurring after lesion have been investigated in a series of previous studies, but a complete analysis of the changes taking place at the level of the axons and the effects on the animals' appearance during the whole regenerative process is still missing. Our goal was to determine the course of events following injury, from impairment to full recovery. Through imaging of the traced damaged nerves, we were able to characterize the pathways followed by fibres during regeneration and end-target re-innervation, while electrophysiology and behavioural observations highlighted the regaining of functional connections between the central brain and periphery, using the contralateral nerve in the same animal as an internal control. The final architecture of a fully regenerated pallial nerve does not exactly mirror the original structure; however, functionality returns to match the phenotype of an intact octopus with no observable impact on the behaviour of the animal. Our findings provide new important scenarios for the study of regeneration in cephalopods and highlight the octopus pallial nerve as a valuable 'model' among invertebrates.


Sujet(s)
Régénération nerveuse/physiologie , Tissu nerveux/traumatismes , Tissu nerveux/physiopathologie , Octopodiformes/physiologie , Récupération fonctionnelle/physiologie , Animaux , Axones/physiologie , Comportement animal , Phénomènes électrophysiologiques , Femelle , Mâle , Octopodiformes/anatomie et histologie , Respiration , Peau/innervation
15.
Med Hypotheses ; 131: 109297, 2019 Oct.
Article de Anglais | MEDLINE | ID: mdl-31443774

RÉSUMÉ

Multiple sclerosis (MS) is an immune-mediated disease which can cause different symptoms due to the involvement of different regions of the central nervous system (CNS). Although this disease is characterized by the demyelination process, the most important feature of the disease is its degenerative nature. This nature is clinically manifested as progressive symptoms, especially in patients' walking, which can even lead to complete debilitation. Therefore, finding a treatment to prevent the degenerative processes is one of the most important goals in MS studies. To better understand the process and the effect of drugs, scientists use animal models which mostly consisting of mouse, rat, and monkey. In evolutionary terms, octopuses belong to the invertebrates which have many substantial differences with vertebrates. One of these differences is related to the nervous system of these organisms, which is divided into central and peripheral parts. The difference lies in the fact that the main volume of this system expands in the limbs of these organisms instead of their brain. This offers a kind of freedom of action and processing strength in the octopus limbs. Also, the brain of these organisms follows a non-somatotopic model. Although the complex actions of this organism are stimulated by the brain, in contrast to the human brain, this activity is not related to a specific region of the brain; rather the entire brain area of the octopus is activated during a process. Indeed, the brain mapping or the topological perception of a particular action, such as moving the limbs, reflects itself in how that activity is distributed in the octopus brain neurons. Accordingly, various actions are known with varying degrees of activity of neurons in the brain of octopus. Another important feature of octopuses is their ability to regenerate defective tissues including the central and peripheral nervous system. These characteristics raise the question of what features can an octopus show when it is used as an organism to create experimental autoimmune encephalomyelitis (EAE). Can the immune system damage of the octopus brain cause a regeneration process? Will the autonomy of the organs reduce the severity of the symptoms? This article seeks to provide evidence to prove that use of octopuses as laboratory samples for generation of EAE may open up new approaches for researchers to better approach MS.


Sujet(s)
Encéphalomyélite auto-immune expérimentale/immunologie , Sclérose en plaques/physiopathologie , Phénomènes physiologiques du système nerveux , Système nerveux/anatomie et histologie , Octopodiformes/anatomie et histologie , Animaux , Axones/physiologie , Membres/traumatismes , Membres/innervation , Membres/physiologie , Hémocytes/physiologie , Humains , Immunité innée , Protéines et peptides de signalisation intercellulaire/physiologie , Sclérose en plaques/immunologie , Phénomènes physiologiques du système nerveux/immunologie , Plasticité neuronale , Octopodiformes/immunologie , Octopodiformes/physiologie , Régénération/physiologie , Spécificité d'espèce , Traumatismes du système nerveux/physiopathologie
16.
Invert Neurosci ; 19(2): 5, 2019 05 10.
Article de Anglais | MEDLINE | ID: mdl-31073644

RÉSUMÉ

Here, we report the findings after application of neurobiotin tracing to pallial and stellar nerves in the mantle of the cephalopod mollusk Octopus vulgaris and to the axial nerve cord in its arm. Neurobiotin backfilling is a known technique in other molluscs, but it is applied to octopus for the first time to be best of our knowledge. Different neural tracing techniques have been carried out in cephalopods to study the intricate neural connectivity of their nervous system, but mapping the nervous connections in this taxon is still incomplete, mainly due to the absence of a reliable tracing method allowing whole-mount imaging. In our experiments, neurobiotin backfilling allowed: (1) imaging of large/thick samples (larger than 2 mm) through optical clearing; (2) additional application of immunohistochemistry on the backfilled tissues, allowing identification of neural structures by coupling of a specific antibody. This work opens a series of future studies aimed to the identification of the neural diagram and connectome of octopus nervous system.


Sujet(s)
Immunohistochimie/méthodes , Voies nerveuses/anatomie et histologie , Octopodiformes/anatomie et histologie , Animaux , Biotine/analogues et dérivés , Agents colorants
17.
Results Probl Cell Differ ; 65: 585-598, 2018.
Article de Anglais | MEDLINE | ID: mdl-30083937

RÉSUMÉ

Octopus vulgaris underwent a radical modification to cope with the benthic lifestyle. It diverged from other cephalopods in terms of body plan, anatomy, behavior, and intelligence. It independently evolved the largest and most complex nervous system and sophisticated behaviors among invertebrates in a separate evolutionary lineage. It is equipped with unusual traits that confer it an incredible evolutionary success: arms capable of a wide range of movements with no skeletal support; developed eyes with a complex visual behavior; vestibular system; primitive "hearing" system; chemoreceptors located in epidermis, suckers, and mouth; and a discrete olfactory organ. As if these were not enough, the occurrence of recently discovered adult neurogenesis and the high level of RNA editing give it a master key to face environmental challenges. Here we provide an overview of some of the winning evolutionary inventions that octopus puts in place such as the capacity to see color, smell by touch, edit own genes, and rejuvenate own brain.


Sujet(s)
Évolution biologique , Octopodiformes/anatomie et histologie , Octopodiformes/physiologie , Animaux , Neurogenèse , Octopodiformes/cytologie , Octopodiformes/génétique
18.
J R Soc Interface ; 15(141)2018 04.
Article de Anglais | MEDLINE | ID: mdl-29643223

RÉSUMÉ

Octopus and cephalopods are able to regenerate injured tissues. Recent advancements in the study of regeneration in cephalopods appear promising encompassing different approaches helping to decipher cellular and molecular machinery involved in the process. However, lack of specific markers to investigate degenerative/regenerative phenomena and inflammatory events occurring after damage is limiting these studies. Label-free multiphoton microscopy is applied for the first time to the transected pallial nerve of Octopus vulgaris Various optical contrast methods including coherent anti-Stokes Raman scattering (CARS), endogenous two-photon excited fluorescence (TPEF) and second harmonic generation (SHG) have been used. We detected cells and structures often not revealed with classical staining methods. CARS highlighted the involvement of haemocytes in building up scar tissue; CARS and TPEF facilitated the identification of degenerating fibres; SHG allowed visualization of fibrillary collagen, revealing the formation of a connective tissue bridge between the nerve stumps, likely involved in axon guidance. Using label-free multiphoton microscopy, we studied the regenerative events in octopus without using any other labelling techniques. These imaging methods provided extremely helpful morpho-chemical information to describe regeneration events. The techniques applied here are species-specific independent and should facilitate the comparison among various animal species.


Sujet(s)
Régénération nerveuse/physiologie , Octopodiformes/physiologie , Animaux , Femelle , Mâle , Microscopie de fluorescence multiphotonique/méthodes , Octopodiformes/anatomie et histologie , Octopodiformes/cytologie , Lésions des nerfs périphériques/imagerie diagnostique , Lésions des nerfs périphériques/anatomopathologie
19.
Curr Biol ; 28(4): R144-R145, 2018 02 19.
Article de Anglais | MEDLINE | ID: mdl-29462576

RÉSUMÉ

Cirrate octopods (Cephalopoda: Cirrata) are among the largest invertebrates of the deep sea. These organisms have long been known to lay single, large egg capsules on hard substrates on the ocean bottom [1], including cold-water octocorals (Anthozoa: Octocorallia). The egg capsule is comprised of an external egg case as well as the chorion and developing embryo. Development in cirrates proceeds for an extended time without parental care [2]. Although juveniles have previously been collected in the midwater [3], cirrate hatchlings have so far never been observed. Here, we provide the first video of a living hatchling and use magnetic resonance imaging (MRI) to analyze its anatomy and assign the specimen to the genus Grimpoteuthis, the so-called dumbo octopods. The specimen's behavior and advanced state of organ development show that cirrate hatchlings possess all morphological features required for movement via fin-swimming, for visually and chemically sensing their environment, and for prey capture. In addition, the presence of a large internal yolk sac reduces the risk of failure at first feeding. These data provide evidence that dumbo octopods hatch as competent juveniles.


Sujet(s)
Animaux nouveau-nés/croissance et développement , Octopodiformes/croissance et développement , Animaux , Animaux nouveau-nés/anatomie et histologie , Animaux nouveau-nés/physiologie , Imagerie par résonance magnétique , Octopodiformes/anatomie et histologie , Octopodiformes/physiologie , Perception olfactive , Comportement prédateur , Natation , Enregistrement sur magnétoscope , Perception visuelle
20.
Bioinspir Biomim ; 12(6): 066003, 2017 Oct 16.
Article de Anglais | MEDLINE | ID: mdl-28767049

RÉSUMÉ

The soft capabilities of biological appendages like the arms of Octopus vulgaris and elephants' trunks have inspired roboticists to develop their robotic equivalents. Although there have been considerable efforts to replicate their morphology and behavior patterns, we are still lagging behind in replicating the dexterity and efficiency of these biological systems. This is mostly due to the lack of development and application of dynamic controllers on these robots which could exploit the morphological properties that a soft-bodied manipulator possesses. The complexity of these high-dimensional nonlinear systems has deterred the application of traditional model-based approaches. This paper provides a machine learning-based approach for the development of dynamic models for a soft robotic manipulator and a trajectory optimization method for predictive control of the manipulator in task space. To the best of our knowledge this is the first demonstration of a learned dynamic model and a derived task space controller for a soft robotic manipulator. The validation of the controller is carried out on an octopus-inspired soft manipulator simulation derived from a piecewise constant strain approximation and then experimentally on a pneumatically actuated soft manipulator. The results indicate that such an approach is promising for developing fast and accurate dynamic models for soft robotic manipulators while being applicable on a wide range of soft manipulators.


Sujet(s)
Biomimétique/méthodes , Algorithmes , Animaux , Éléphants/anatomie et histologie , Éléphants/physiologie , , Octopodiformes/anatomie et histologie , Octopodiformes/physiologie
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