Transcriptome Analysis and Ultrastructure Observation Reveal that Hawthorn Fruit Softening Is due to Cellulose/Hemicellulose Degradation

Softening, a common phenomenon in many fruits, is a well coordinated and genetically determined process. However, the process of flesh softening during ripening has rarely been described in hawthorn. In this study, we found that ‘Ruanrou Shanlihong 3 Hao’ fruits became softer during ripening, whereas ‘Qiu JinXing’ fruits remained hard. At late developmental stages, the firmness of ‘Ruanrou Shanlihong 3 Hao’ fruits rapidly declined, and that of ‘Qiu JinXing’ fruits remained essentially unchanged. According to transmission electron microscopy (TEM), the middle lamella of ‘Qiu JinXing’ and ‘Ruanrou Shanlihong 3 Hao’ fruit flesh was largely degraded as the fruits matured. Microfilaments in ‘Qiu JinXing’ flesh were arranged close together and were deep in color, whereas those in ‘Ruanrou Shanlihong 3 Hao’ fruit flesh were arranged loosely, partially degraded and light in color. RNA-Seq analysis yielded approximately 46.72 Gb of clean data and 72,837 unigenes. Galactose metabolism and pentose and glucuronate interconversions are involved in cell wall metabolism, play an important role in hawthorn texture. We identified 85 unigenes related to the cell wall between hard- and soft-fleshed hawthorn fruits. Based on data analysis and real-time PCR, we suggest that β-GAL and PE4 have important functions in early fruit softening. The genes Ffase, Gns, α-GAL, PE63, XTH and CWP, which are involved in cell wall degradation, are responsible for the different textures of hawthorn fruits. Thus, we hypothesize that the different textures of ‘Qiu JinXing’ and ‘Ruanrou Shanlihong 3 Hao’ fruits at maturity mainly result from cellulose/hemicelluloses degradation rather than from lamella degradation. Overall, we propose that different types of hydrolytic enzymes in cells interact to degrade the cell wall, resulting in ultramicroscopic Structure changes in the cell wall and, consequently, fruit softening. These results provide fundamental insight regarding the mechanisms by which hawthorn fruits acquire different textures and also lay a solid foundation for further research

Training-Free Instance Segmentation from Semantic Image Segmentation Masks

In recent years, the development of instance segmentation has garnered significant attention in a wide range of applications. However, the training of a fully-supervised instance segmentation model requires costly both instance-level and pixel-level annotations. In contrast, weakly-supervised instance segmentation methods (i.e., with image-level class labels or point labels) struggle to satisfy the accuracy and recall requirements of practical scenarios. In this paper, we propose a novel paradigm for instance segmentation called training-free instance segmentation (TFISeg), which achieves instance segmentation results from image masks predicted using off-the-shelf semantic segmentation models. TFISeg does not require training a semantic or/and instance segmentation model and avoids the need for instance-level image annotations. Therefore, it is highly efficient. Specifically, we first obtain a semantic segmentation mask of the input image via a trained semantic segmentation model. Then, we calculate a displacement field vector for each pixel based on the segmentation mask, which can indicate representations belonging to the same class but different instances, i.e., obtaining the instance-level object information. Finally, instance segmentation results are obtained after being refined by a learnable category-agnostic object boundary branch. Extensive experimental results on two challenging datasets and representative semantic segmentation baselines (including CNNs and Transformers) demonstrate that TFISeg can achieve competitive results compared to the state-of-the-art fully-supervised instance segmentation methods without the need for additional human resources or increased computational costs. The code is available at: TFISegComment: 14 pages,5 figure

Characterizing the temporally stable structure of community evolution in intra-urban origin-destination networks

Intra-urban origin-destination (OD) network communities evolve throughout the day, indicating changing groups of closely connected regions. Under this variation, groups of regions with high consistency of community affiliation characterize the temporally stable structure of the evolution process, aiding in comprehending urban dynamics. However, how to quantify this consistency and identify these groups are open questions. In this study, we introduce the consensus OD network to quantify the consistency of community affiliation among regions. Furthermore, the temporally stable community decomposition method is proposed to identify groups of regions with high internal and low external consistency (named "stable groups"), where each group consists of temporally stable cores and attaching peripheries. Wuhan taxi data is used to verify our methods. On the hourly time scale, eleven stable groups containing 82.9% of regions are identified. This high percentage suggests that dynamic communities can be well organized via cores. Moreover, stable groups are spatially closed and more likely to distribute within a single district and separated by water bodies. Cores exhibit higher POI entropy and more healthcare and shopping services than peripheries. Our methods and empirical findings contribute to some practical issues, such as urban area division, polycentric evaluation and construction, and infectious disease control

Health monitoring device design and application for large synchronously excited multi-shaker vibration test facility

There are different kinds of equipments distributed in different locations for a large complicated multi-shaker vibration test facility, so it is challenging to monitor the real state of test facility thoroughly during its operation. Long-term operation of this test facility will lead to the degradation of reliability and malfunction, and sometimes the emergency stop of the whole test system that threatens the safety of the spacecraft seriously. This paper presents in detail the design and application of a set of health monitoring device for a large multi-shaker vibration test facility which is capable of monitoring the operation state in real time and predicting the potential malfunction of the whole test facility to ensure the reliability of this large test system and safety of the spacecraft during its environmental vibration test

Myricetin alleviates H2O2-induced senescence and apoptosis in rat nucleus pulposus-derived mesenchymal stem cells

Introduction. Transplantation of mesenchymal stem cells (MSCs) has been reported to be a novel promising target for the regeneration of degenerated intervertebral discs (IVDs). However, the culture and survival limitations of MSCs remain challenging for MSC-based biological therapy. Myricetin, a common natural flavonoid, has been suggested to possess antiaging and antioxidant abilities. Therefore, we investigated the biological function of myricetin, and its related mechanisms involving cell senescence in intervertebral disc degeneration (IDD). Material and methods. The nucleus pulposus-derived mesenchymal stem cells (NPMSCs) were isolated from 4-month-old Sprague-Dawley (SD) rats and identified by examining surface markers and multipotent differentiation. Rat NPMSCs were cultured in an MSC culture medium or culture medium with different concentrations of H2O2. Myricetin or the combination of myricetin and EX527 were added to the culture medium to investigate the effects of myricetin. Cell viability was evaluated by cell counting kit-8 assays (CCK-8). The apoptosis rate was determined using Annexin V/PI dual staining. The mitochondrial membrane potential (MMP) was analyzed by a fluorescence microscope after JC-1 staining. The cell senescence was determined by SA-β-Gal staining. MitoSOX green was used to selectively estimate mitochondrial reactive oxygen species (ROS) Apoptosis-associated proteins (Bax, Bcl2, and cleaved caspase-3), senescence markers (p16, p21, and p53), and SIRT1/PGC-1α signaling pathway-related proteins (SIRT1 and PGC-1α) were evaluated by western blotting. Results. The cells isolated from nucleus pulposus (NP) tissues met the criteria for MSCs. Myricetin showed no cytotoxicity up to a concentration of 100 μM in rat NPMSCs cultured for 24 h. Myricetin pretreatment exhibited protective effects against H2O2-induced apoptosis. Myricetin could also alleviate H2O2-induced mitochondrial dysfunctions of increased mitochondrial ROS production and reduced MMP. Moreover, myricetin pretreatment delayed rat NPMSC senescence, as evidenced by decreased senescence indicators and reduced SA-β-Gal activity. Pretreatment of NPMSCs with 10 μM EX527, a selective inhibitor of SIRT1, prior to exposure to 100 μM H2O2, reversed the inhibitory effects of myricetin on cell apoptosis. Conclusions. Myricetin could affect the SIRT1/PGC-1α pathway to protect mitochondrial functions and alleviate cell senescence in H2O2-treated NPMSCs

The Ginger-shaped Asteroid 4179 Toutatis: New Observations from a Successful Flyby of Chang'e-2

On 13 December 2012, Chang'e-2 conducted a successful flyby of the near-Earth asteroid 4179 Toutatis at a closest distance of 770 $\pm$ 120 meters from the asteroid's surface. The highest-resolution image, with a resolution of better than 3 meters, reveals new discoveries on the asteroid, e.g., a giant basin at the big end, a sharply perpendicular silhouette near the neck region, and direct evidence of boulders and regolith, which suggests that Toutatis may bear a rubble-pile structure. Toutatis' maximum physical length and width are (4.75 $\times$ 1.95 km) $\pm$10$\%$, respectively, and the direction of the +$z$ axis is estimated to be (250$\pm$5$^\circ$, 63$\pm$5$^\circ$) with respect to the J2000 ecliptic coordinate system. The bifurcated configuration is indicative of a contact binary origin for Toutatis, which is composed of two lobes (head and body). Chang'e-2 observations have significantly improved our understanding of the characteristics, formation, and evolution of asteroids in general.Comment: 21 pages, 3 figures, 1 tabl

Crystal structure of rhodopsin bound to arrestin by femtosecond X-ray laser.

G-protein-coupled receptors (GPCRs) signal primarily through G proteins or arrestins. Arrestin binding to GPCRs blocks G protein interaction and redirects signalling to numerous G-protein-independent pathways. Here we report the crystal structure of a constitutively active form of human rhodopsin bound to a pre-activated form of the mouse visual arrestin, determined by serial femtosecond X-ray laser crystallography. Together with extensive biochemical and mutagenesis data, the structure reveals an overall architecture of the rhodopsin-arrestin assembly in which rhodopsin uses distinct structural elements, including transmembrane helix 7 and helix 8, to recruit arrestin. Correspondingly, arrestin adopts the pre-activated conformation, with a ∼20° rotation between the amino and carboxy domains, which opens up a cleft in arrestin to accommodate a short helix formed by the second intracellular loop of rhodopsin. This structure provides a basis for understanding GPCR-mediated arrestin-biased signalling and demonstrates the power of X-ray lasers for advancing the frontiers of structural biology

Qishen Yiqi dripping pills for chronic ischaemic heart failure:results of the CACT-IHF randomized clinical trial

10.1002/ehf2.12980ESC Heart Failure763881-389