Multi-step self-guided pathways for shape-changing metamaterials

Multi-step pathways, constituted of a sequence of reconfigurations, are central to a wide variety of natural and man-made systems. Such pathways autonomously execute in self-guided processes such as protein folding and self-assembly, but require external control in macroscopic mechanical systems, provided by, e.g., actuators in robotics or manual folding in origami. Here we introduce shape-changing mechanical metamaterials, that exhibit self-guided multi-step pathways in response to global uniform compression. Their design combines strongly nonlinear mechanical elements with a multimodal architecture that allows for a sequence of topological reconfigurations, i.e., modifications of the topology caused by the formation of internal self-contacts. We realized such metamaterials by digital manufacturing, and show that the pathway and final configuration can be controlled by rational design of the nonlinear mechanical elements. We furthermore demonstrate that self-contacts suppress pathway errors. Finally, we demonstrate how hierarchical architectures allow to extend the number of distinct reconfiguration steps. Our work establishes general principles for designing mechanical pathways, opening new avenues for self-folding media, pluripotent materials, and pliable devices in, e.g., stretchable electronics and soft robotics.Comment: 16 pages, 3 main figures, 10 extended data figures. See https://youtu.be/8m1QfkMFL0I for an explanatory vide

Discovery of Novel Small Molecule Activators of β-Catenin Signaling

Wnt/β-catenin signaling plays a major role in embryonic development and adult stem cell maintenance. Reduced activation of the Wnt/β-catenin pathway underlies neurodegenerative disorders and aberrations in bone formation. Screening of a small molecule compound library with a β-galactosidase fragment complementation assay measuring β-catenin nuclear entry revealed bona fide activators of β-catenin signaling. The compounds stabilized cytoplasmic β-catenin and activated β–catenin-dependent reporter gene activity. Although the mechanism through which the compounds activate β-catenin signaling has yet to be determined, several key regulators of Wnt/β-catenin signaling, including glycogen synthase kinase 3 and Frizzled receptors, were excluded as the molecular target. The compounds displayed remarkable selectivity, as they only induced β-catenin signaling in a human osteosarcoma U2OS cell line and not in a variety of other cell lines examined. Our data indicate that differences in cellular Wnt/β-catenin signaling machinery can be exploited to identify cell type-specific activators of Wnt/β-catenin signaling

Modelling hysteresis in the water sorption and drying shrinkage of cement paste

Shrinkage can be critical for the strength and durability of drying cement pastes. Shrinkage becomes particularly severe at very low relative humidity, < 20%, which can be met in some activities involving extreme temperatures. Experiments and simulations suggest that small pores in the cement paste, with approximate thickness ≤ 1 nm, stay saturated unless the humidity drops below 20%. Here we suggest that this pore size can define two different categories of pores in the paste: pores thicker than 1 nm, where the Kelvin's equation and the corresponding capillary (Laplace) pressure apply, and pores thinner than 1 nm, which can be considered as part of the solid skeleton if the humidity stays above 20%. We show that a continuum model, incorporating a pore-blocking mechanism for desorption and equilibrium thermodynamics for adsorption, explains well the sorption hysteresis for a paste that remains above ∼ 20%. At lower humidities, we assume that (1) during adsorpion water re-enters the smallest pores throughout the entire RH range (supported by experiments and simulations) and (2) there exists a simple linear relationship between water and strain in the smallest pores. These minimal assumptions are sufficient to explain the low-humidity hysteresis of water content and strain, but the underlying mechanistic explanation is still an open question. Combining the low-humidity and high-humidity models allows capturing the entire drying and rewetting hysteresis, and provides parameters to predict the corresponding dimensional changes

Citocinas e proteínas de fase aguda do soro como marcadores de regressão da resposta inflamatória ao tratamento da tuberculose pulmonar Cytokines and acute phase serum proteins as markers of inflammatory regression during the treatment of pulmonary tuberculosis

OBJETIVO: Analisar o padrão de citocinas pró- e antiinflamatórias e da resposta de fase aguda (RFA) como marcadores de resposta ao tratamento da tuberculose pulmonar. MÉTODOS: Determinação dos níveis de interferon-gama (IFN-&#947;), tumor necrosis factor-alpha (TNF-&#945;, fator de necrose tumoral-alfa), interleucina-10 (IL-10) e transforming growth factor-beta (TGF-&#946;, fator transformador de crescimento-beta), pelo método ELISA, em sobrenadante de cultura de células mononucleares do sangue periférico e monócitos, assim como dos níveis de proteínas totais, albumina, globulinas, alfa-1-glicoproteína ácida (AGA), proteína C reativa (PCR) e velocidade de hemossedimentação (VHS) em 28 doentes com tuberculose pulmonar, em três tempos: antes (T0), aos três meses (T3) e aos seis meses (T6) de tratamento, em relação aos controles saudáveis, em um único tempo. RESULTADOS: Os pacientes apresentaram valores maiores de citocinas e RFA que os controles em T0, com diminuição em T3 e diminuição (TNF-&#945;, IL-10, TGF-&#946;, AGA e VHS) ou normalização (IFN-&#947; e PCR) em T6. CONCLUSÕES: PCR, AGA e VHS são possíveis marcadores para auxiliar no diagnóstico de tuberculose pulmonar e na indicação de tratamento de indivíduos com baciloscopia negativa; PCR (T0 > T3 > T6 = referência) pode também ser marcador de resposta ao tratamento. Antes do tratamento, o perfil Th0 (IFN-&#947;, IL-10, TNF-&#945; e TGF-&#946;), indutor de e protetor contra inflamação, prevaleceu nos pacientes; em T6, prevaleceu o perfil Th2 (IL-10, TNF-&#945; e TGF-&#946;), protetor contra efeito nocivo pró-inflamatório do TNF-&#945; ainda presente. O comportamento do IFN-&#947; (T0 > T3 > T6 = controle) sugere sua utilização como marcador de resposta ao tratamento.<br>OBJECTIVE: To evaluate the pattern of pro-inflammatory cytokines, anti-inflammatory cytokines and the acute phase response (APR) as markers of the response to treatment of pulmonary tuberculosis. METHODS: Twenty-eight patients with pulmonary tuberculosis were evaluated at three time points: pretreatment (T0), treatment month 3 (T3) and treatment month 6 (T6). Levels of interferon-gamma (IFN-&#947;), tumor necrosis factor-alpha (TNF-&#945;), interleukine-10 (IL-10) and transforming growth factor-beta (TGF-&#946;) were determined using ELISA in the supernatant of peripheral blood mononuclear cell and monocyte culture. Levels of total protein, albumin, globulins, C-reactive protein (CRP), alpha-1-acid glycoprotein (AAG) and erythrocyte sedimentation rate (ESR) were also determined. All of these parameters were also evaluated, only once, in a group of healthy controls. RESULTS: In relation to controls, patients presented cytokine levels and APR that were higher at T0, lower at T3 and either lower (TNF-&#945;, IL-10, TGF-&#946;, AAG and ESR) or normal (IFN-&#947; and CRP) at T6. CONCLUSIONS: For individuals with negative smear sputum microscopy, CRP, AAG and ESR are potential markers of pulmonary tuberculosis and of the need for treatment; CRP (T0 > T3 > T6 = reference) can also be a marker of treatment response. In the patients, the Th0 profile (IFN-&#947;, IL-10, TNF-&#945; and TGF-&#946;), inducer of and protector against inflammation, predominated at T0, whereas the Th2 profile (IL-10, TNF-&#945; and TGF-&#946;), protecting against the harmful pro-inflammatory effect of the remaining TNF-&#945;, predominated at T6. The behavior of IFN-&#947; (T0 > T3 > T6 = controls) suggests its use as a marker of treatment response

Spectral band decomposition combined with nonlinear models: application to indoor formaldehyde concentration forecasting

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