Thermal storage/management system with phase change materials for building

Peer reviewe

An exact solution of spherical mean-field plus orbit-dependent non-separable pairing model with two non-degenerate j-orbits

An exact solution of nuclear spherical mean-field plus orbit-dependent non-separable pairing model with two non-degenerate j-orbits is presented. The extended one-variable Heine-Stieltjes polynomials associated to the Bethe ansatz equations of the solution are determined, of which the sets of the zeros give the solution of the model, and can be determined relatively easily. A comparison of the solution to that of the standard pairing interaction with constant interaction strength among pairs in any orbit is made. It is shown that the overlaps of eigenstates of the model with those of the standard pairing model are always large, especially for the ground and the first excited state. However, the quantum phase crossover in the non-separable pairing model cannot be accounted for by the standard pairing interaction.Comment: 5 pages, 1 figure, LaTe

γ -soft rotor with configuration mixing in the O(6) limit of the interacting boson model

To describe obvious intruder states and nonzero quadrupole moments of γ-soft nuclei such as Pt194, a rotor extension plus intruder configuration mixing with 2n-particle and 2n-hole configurations from n=0 up to n→ in the O(6) (γ-unstable) limit of the interacting boson model is proposed. It is shown that the configuration mixing scheme keeps the lower part of the γ-unstable spectrum unchanged and generates the intruder states due to the mixing. It is further shown that almost all low-lying levels below 2.17 MeV in Pt194 can be well described by modifying the O(6) quadrupole-quadrupole interaction into an exponential form. The third-order term needed for a rotor realization in the interacting boson model seems necessary to produce nonzero quadrupole moments with the correct sign

Clustered microRNAs' coordination in regulating protein-protein interaction network

<p>Abstract</p> <p>Background</p> <p>MicroRNAs (miRNAs), a growing class of small RNAs with crucial regulatory roles at the post-transcriptional level, are usually found to be clustered on chromosomes. However, with the exception of a few individual cases, so far little is known about the functional consequence of this conserved clustering of miRNA loci. In animal genomes such clusters often contain non-homologous miRNA genes. One hypothesis to explain this heterogeneity suggests that clustered miRNAs are functionally related by virtue of co-targeting downstream pathways.</p> <p>Results</p> <p>Integrating of miRNA cluster information with protein protein interaction (PPI) network data, our research supports the hypothesis of the functional coordination of clustered miRNAs and links it to the topological features of miRNAs' targets in PPI network. Specifically, our results demonstrate that clustered miRNAs jointly regulate proteins in close proximity of the PPI network. The possibility that two proteins yield to this coordinated regulation is negatively correlated with their distance in PPI network. Guided by the knowledge of this preference, we found several network communities enriched with target genes of miRNA clusters. In addition, our results demonstrate that the variance of this propensity can also partly be explained by protein's connectivity and miRNA's conservation.</p> <p>Conclusion</p> <p>In summary, this work supports the hypothesis of intra-cluster coordination and investigates the extent of this coordination.</p

Mechanical overloading induces GPX4-regulated chondrocyte ferroptosis in osteoarthritis via Piezo1 channel facilitated calcium influx

Introductions: Excessive mechanical stress is closely associated with cell death in various conditions. Exposure of chondrocytes to excessive mechanical loading leads to a catabolic response as well as exaggerated cell death. Ferroptosis is a recently identified form of cell death during cell aging and degeneration. However, it's potential association with mechanical stress remains to be illustrated. Objectives: To identify whether excessive mechanical stress can cause ferroptosis. To explore the role of mechanical overloading in chondrocyte ferroptosis. Methods: Chondrocytes were collected from loading and unloading zones of cartilage in patients with osteoarthritis (OA), and the ferroptosis phenotype was analyzed through transmission electron microscope and microarray. Moreover, the relationship between ferroptosis and OA was analyzed by GPX4-conditional knockout (Col2a1-CreERT: GPX4flox/flox) mice OA model and chondrocytes cultured with high strain mechanical stress. Furthermore, the role of Piezo1 ion channel in chondrocyte ferroptosis and OA development was explored by using its inhibitor (GsMTx4) and agonist (Yoda1). Additionally, chondrocyte was cultured in calcium-free medium with mechanical stress, and ferroptosis phenotype was tested. Results: Human cartilage and mouse chondrocyte experiments revealed that mechanical overloading can induce GPX4-associated ferroptosis. Conditional knockout of GPX4 in cartilage aggravated experimental OA process, while additional treatment with ferroptosis suppressor protein (FSP-1) and coenzyme Q10 (CoQ10) abated OA development in GPX4-CKO mice. In mouse OA model and chondrocyte experiments, inhibition of Piezo1 channel activity increased GPX4 expression, attenuated ferroptosis phenotype and reduced the severity of osteoarthritis. Additionally, high strain mechanical stress induced ferroptosis damage in chondrocyte was largely abolished by blocking calcium influx through calcium-free medium. Conclusions: Our findings show that mechanical overloading induces ferroptosis through Piezo1 activation and subsequent calcium influx in chondrocytes, which might provide a potential target for OA treatment

Association of polymicrobial interactions with dental caries development and prevention

Dental caries is a common oral disease. In many cases, disruption of the ecological balance of the oral cavity can result in the occurrence of dental caries. There are many cariogenic microbiota and factors, and their identification allows us to take corresponding prevention and control measures. With the development of microbiology, the caries-causing bacteria have evolved from the traditional single Streptococcus mutans to the discovery of oral symbiotic bacteria. Thus it is necessary to systematically organized the association of polymicrobial interactions with dental caries development. In terms of ecology, caries occurs due to an ecological imbalance of the microbiota, caused by the growth and reproduction of cariogenic microbiota due to external factors or the disruption of homeostasis by one’s own factors. To reduce the occurrence of dental caries effectively, and considering the latest scientific viewpoints, caries may be viewed from the perspective of ecology, and preventive measures can be taken; hence, this article systematically summarizes the prevention and treatment of dental caries from the aspects of ecological perspectives, in particular the ecological biofilm formation, bacterial quorum sensing, the main cariogenic microbiota, and preventive measures