44 research outputs found

    A self-organized synthetic morphogenic liposome responds with shape changes to local light cues

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    Reconstituting artificial proto-cells capable of transducing extracellular signals into cytoskeletal changes can reveal fundamental principles of how non-equilibrium phenomena in cellular signal transduction affect morphogenesis. Here, we generated a Synthetic Morphogenic Membrane System (SynMMS) by encapsulating a dynamic microtubule (MT) aster and a light-inducible signaling system driven by GTP/ATP chemical potential into cell-sized liposomes. Responding to light cues in analogy to morphogens, this biomimetic design embodies basic principles of localized Rho-GTPase signal transduction that generate an intracellular MT-regulator signaling gradient. Light-induced signaling promotes membrane-deforming growth of MT-filaments by dynamically elevating the membrane-proximal tubulin concentration. The resulting membrane deformations enable recursive coupling of the MT-aster with the signaling system, which generates global self-organized morphologies that reorganize towards local external cues in dependence on prior shape. SynMMS thereby signifies a step towards bio-inspired engineering of self-organized cellular morphogenesis

    Response of prairie voles, Microtus ochrogaster (Rodentia, Arvicolidae), to scent over-marks of two same-sex conspecifics: A test of the scent-masking hypothesis

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    Previous work shows that after investigating a same-sex over-mark, two nonmonogamous species, meadow voles and golden hamsters, preferred the odor of the top-scent donor to that of the bottom-scent donor, and behaved as the odor of the bottom-scent donor was not familiar. This finding supported the scent-masking hypothesis; one of three hypotheses suggested previously to account for how an animal responds to the overlapping scent marks of two same-sex conspecifics. The present experiments tested whether one of these hypotheses, either scent-masking, scent-bulletin-board, or scent-blending, predicts how a monogamous species, the prairie vole, responds to such over-marks. Our data show that none of the three hypotheses adequately describes the way in which prairie voles respond to conspecific over-marks. Although prairie voles preferred the top scent to the bottom scent, they behaved as if the latter scent was familiar and less important than a novel scent (a scent not part of the over-mark). Overall, the data suggest that the manner in which males and females respond to same-sex over-marks reflects the different tactics they may use to attract and compete with conspecifics in monogamous and nonmonogamous species

    Meadow voles and prairie voles differ in the length of time they prefer the top-scent donor of an over-mark

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    Scent over-marking occurs when one individual places its scent mark on top of one deposited by a conspecific. Studies have shown that animals investigating an over-mark later behave as if the top-scent mark is more important than the bottom-scent mark. Differences in response to over-marks may reflect differences in social and mating systems. Here, we ascertained the length of time that meadow voles (Microtus pennsylvanicus) and prairie voles (Microtus ochrogaster), exposed to an over-mark, maintain a preference for the mark of the top-scent donor compared with that of the bottom-scent donor. If voles had no previous sexual experience with their top-scent and bottom-scent donors, male and female meadow voles maintained a preference for their top-scent donor\u27s mark over their bottom-scent donor\u27s mark for 48 h. In contrast, male and female prairie voles maintained such preferences for 24 h and 12 h, respectively. If voles had prior sexual experience with either their top- or bottom-scent donor, such experience did not affect the length of time meadow voles and male prairie voles maintained a preference for their top-scent donor. Female prairie voles maintained a 12-h preference for the top-scent mark if it belonged to the mate. If the mate was the bottom-scent donor, female prairie voles showed no preference for it or the top-scent mark. These findings are discussed within the framework that an association may exist between the manner in which voles respond to over-marks and their social and mating systems

    A synthetic morphogenic perceptory cell

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    We reconstituted a Synthetic Morphogenic Perceptory System (SynMPS) by encapsulating a dynamic cytoskeletal microtubule (MT)-aster together with a light-actuated signaling system in a liposome. SynMPS responds to light with self-organized morphological state transitions that manifest as self-amplifying membrane deformations generated by the MT-aster recursively interacting with the signaling system. We demonstrate that the perception and response to external light pattern stimuli are shaped by prior exposures and the ensuing morphological states. The interdependence between cytoskeletal dynamics, membrane shape, and signaling thus generated a minimal out-of-equilibrium ‘life-like’ system that mimics context dependent morphological responses of cells to external cues

    The function of embryonic stem cell-expressed Ras (E-Ras), a unique Ras family member, correlates with its additional motifs and its structural properties

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    E-RAS is a member of the RAS family specifically expressed in embryonic stem cells, gastric tumors, and hepatic stellate cells. Unlike classical RAS isoforms (H-, N-, and K-RAS4B), E-RAS has, in addition to striking and remarkable sequence deviations, an extended 38-amino acid-long unique N-terminal region with still unknown functions. We investigated the molecular mechanism of E-RAS regulation and function with respect to its sequence and structural features. We found that N-terminal extension of E-RAS is important for E-RAS signaling activity. E-RAS protein most remarkably revealed a different mode of effector interaction as compared with H-RAS, which correlates with deviations in the effector-binding site of E-RAS. Of all these residues, tryptophan 79 (arginine 41 in H-RAS), in the interswitch region, modulates the effector selectivity of RAS proteins from H-RAS to E-RAS features
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