Highly Efficient Separation of BTEX via Amide Naphthotube Cavity-Confined Tandem C/N-H···π Interactions.

The separation of BTEX [benzene, toluene, ethylbenzene (EB), and xylene isomers] poses a huge challenge in the industry, attributed to their similar structures and physical properties. Supramolecular compounds show great promise for hydrocarbon separation. Herein, we designed two pairs of endo-functionalized amide naphthotubes with methyl and benzyl side chains, which were first employed as chromatographic separation materials and exhibited high shape-selectivity for BTEX. In particular, the amide naphthotubes with methyl side chains provided complete separation toward BTEX and anti-3a showed high selectivity for the p-xylene over other isomers with αPX/OX = 9.34, αPX/MX = 5.50, and αPX/EB = 4.30. The mechanism of BTEX separation originates from the synergistic effect of specially confined tandem N-H···π and C-H···π interactions toward aromatic compounds. The findings of this research show promise for practical applications in efficiently separating crucial aromatic isomers.

High-resolution self-corrected single-pixel imaging through dynamic and complex scattering media: erratum.

We correct typographical errors in our paper [Opt. Express31, 23027 (2023)10.1364/OE.489808]. The corrections have no influence on the results and conclusions of the original paper.

High-resolution ghost imaging through complex scattering media via a temporal correction: erratum.

We correct a typographical error in our Letter [Opt. Lett.47, 3692 (2022)10.1364/OL.463897]. The corrections have no influence on the results and conclusions of the original Letter.

Discriminatory fluorescence and FRET in the chiral-perovskite/RhB system.

Förster resonance energy transfer (FRET) holds a significant position in various natural and artificial systems, especially within donor-acceptor systems encompassing chiral components. Despite extensive investigations, a clear understanding of the effects of chirality and FRET on discriminatory fluorescence remains elusive. Here, chiral perovskite nanowires (CPNWs) and achiral rhodamine B (RhB) are employed to examine the FRET and discriminatory fluorescence behavior in a donor-acceptor system involving a chiral nanostructure. A notable FRET from the CPNWs to RhB is observed, along with circular dichroism (CD) and circularly polarized luminescence (CPL) activities in RhB. Although the FRET interaction remains consistent over time, a notable inversion in the polarity preference of the CD and CPL of RhB is observed. This reveals that the discriminatory fluorescence of the acceptor arises from the electromagnetic influence of the chiral donor. These findings elucidate that "chirality", as a property related to spatial orientation, cannot accompany the transfer of energy (which is a scalar) from chiral nanostructures to achiral molecules, which helps advance the understanding of the discriminatory fluorescence in the donor-acceptor system with a chiral nanostructure.

Activation of D2-like dopamine receptors improves the neuronal network and cognitive function of PPT1KI mice.

Palmitoyl-protein thioesterase 1 (PPT1) is a lysosomal depalmitoylation enzyme that mediates protein posttranslational modifications. Loss-of-function mutation of PPT1 causes a failure of the lysosomal degradation of palmitoylated proteins and results in a congenital disease characterized by progressive neuronal degeneration referred to as infantile neuronal ceroid lipofuscinosis (INCL). A mouse knock-in model of PPT1 (PPT1-KI) was established by introducing the R151X mutation into exon 5 of the PPT1 gene, which exhibited INCL-like pathological lesions. We previously reported that hippocampal γ oscillations were impaired in PPT1 mice. Hippocampal γ oscillations can be enhanced by selective activation of the dopamine D4 receptor (DR4), a dopamine D2-like receptor. In this study, we investigated the changes in DR expression and the effects of dopamine and various DR agonists on neural network activity, cognition and motor function in PPT1KI mice. Cognition and motor defects were evaluated via Y-maze, novel object recognition and rotarod tests. Extracellular field potentials were elicited in hippocampal slices, and neuronal network oscillations in the gamma frequency band (γ oscillations) were induced by perfusion with kainic acid (200 nM). PPT1KI mice displayed progressive impairments in γ oscillations and hippocampus-related memory, as well as abnormal expression profiles of dopamine receptors with preserved expression of DR1 and 3, increased membrane expression of DR4 and decreased DR2 levels. The immunocytochemistry analysis revealed the colocalization of PPT1 with DR4 or DR2 in the soma and large dendrites of both WT and PPT1KI mice. Immunoprecipitation confirmed the interaction between PPT1 and DR4 or DR2. The impaired γ oscillations and cognitive functions were largely restored by the application of exogenous dopamine, the selective DR2 agonist quinpirole or the DR4 agonist A412997. Furthermore, the administration of A412997 (0.5 mg/kg, i.p.) significantly upregulated the activity of CaMKII in the hippocampus of 5-month-old PPT1KI mice. Collectively, these results suggest that the activation of D2-like dopamine receptors improves cognition and network activity in PPT1KI mice and that specific DR subunits may be potential targets for the intervention of neurodegenerative disorders, such as INCL.

A novel dual-epigenetic inhibitor enhances recombinant monoclonal antibody expression in CHO cells.

Epigenetic regulation plays a central role in the regulation of a number of cellular processes such as proliferation, differentiation, cell cycle, and apoptosis. In particular, small molecule epigenetic modulators are key elements that can effectively influence gene expression by precisely regulating the epigenetic state of cells. To identify useful small-molecule regulators that enhance the expression of recombinant proteins in Chinese hamster ovary (CHO) cells, we examined a novel dual-HDAC/LSD1 inhibitor I-4 as a supplement for recombinant CHO cells. Treatment with 2 µM I-4 was most effective in increasing monoclonal antibody production. Despite cell cycle arrest at the G1/G0 phase, which inhibits cell growth, the addition of the inhibitor at 2 µM to monoclonal antibody-expressing CHO cell cultures resulted in a 1.94-fold increase in the maximal monoclonal antibody titer and a 2.43-fold increase in specific monoclonal antibody production. In addition, I-4 significantly increased the messenger RNA levels of the monoclonal antibody and histone H3 acetylation and methylation levels. We also investigated the effect on HDAC-related isoforms and found that interference with the HDAC5 gene increased the monoclonal antibody titer by 1.64-fold. The results of this work provide an effective method of using epigenetic regulatory strategies to enhance the expression of recombinant proteins in CHO cells. KEY POINTS: • HDAC/LSD1 dual-target small molecule inhibitor can increase the expression level of recombinant monoclonal antibodies in CHO cells. • By affecting the acetylation and methylation levels of histones in CHO cells and downregulating HDAC5, the production of recombinant monoclonal antibodies increased. • It provides an effective pathway for applying epigenetic regulation strategies to enhance the expression of recombinant proteins.

Injectable ultrasound-powered bone-adhesive nanocomposite hydrogel for electrically accelerated irregular bone defect healing.

The treatment of critical-size bone defects with irregular shapes remains a major challenge in the field of orthopedics. Bone implants with adaptability to complex morphological bone defects, bone-adhesive properties, and potent osteogenic capacity are necessary. Here, a shape-adaptive, highly bone-adhesive, and ultrasound-powered injectable nanocomposite hydrogel is developed via dynamic covalent crosslinking of amine-modified piezoelectric nanoparticles and biopolymer hydrogel networks for electrically accelerated bone healing. Depending on the inorganic-organic interaction between the amino-modified piezoelectric nanoparticles and the bio-adhesive hydrogel network, the bone adhesive strength of the prepared hydrogel exhibited an approximately 3-fold increase. In response to ultrasound radiation, the nanocomposite hydrogel could generate a controllable electrical output (-41.16 to 61.82 mV) to enhance the osteogenic effect in vitro and in vivo significantly. Rat critical-size calvarial defect repair validates accelerated bone healing. In addition, bioinformatics analysis reveals that the ultrasound-responsive nanocomposite hydrogel enhanced the osteogenic differentiation of bone mesenchymal stem cells by increasing calcium ion influx and up-regulating the PI3K/AKT and MEK/ERK signaling pathways. Overall, the present work reveals a novel wireless ultrasound-powered bone-adhesive nanocomposite hydrogel that broadens the therapeutic horizons for irregular bone defects.

Lung adenocarcinoma discovered during the follow-up of lung-dominant connective tissue disease: a case report and literature review.

Interstitial lung disease (ILD) can lead to lung cancer, which brings great challenges to differential diagnosis and comprehensive treatment. However, the clinical features of lung-dominant connective tissue disease (LD-CTD) related ILD combined with lung cancer has not been validated. We report the case of an 80-year-old woman with LD-CTD treated regularly with nintedanib who presented progressive dyspnoea and hypoxemia after recurrent viral infections. Her chest computed tomography (CT) showed aggravated interstitial fibrosis in both lower lungs with moderate right pleural effusion. Clinicians should be alert to lung cancer in patients who are experiencing poor responsiveness to treatment or acute progression of ILD. The available literatures about the differential diagnosis of clinical manifestations, imaging, treatment and prognosis of LD-CTD are reviewed and discussed in this study.

[Research progress on the mechanism of the impact of maternal childhood trauma on intergenerational transmission]. / æ¯äº²ç«¥å¹´æœŸåˆ›ä¼¤å¯¹ä»£é™ ä¼ é€’å½±å“æœºåˆ¶çš„ç ”ç©¶è¿›å±•.

Childhood trauma refers to trauma experiences encountered during childhood and adolescence. Maternal childhood trauma experiences have a lasting impact on the next generation, affecting their physical and mental well-being. The mechanisms involved include the hypothalamic-pituitary-adrenal axis, inflammatory factors, brain structure and function, gene interactions, and parenting styles. This paper systematically reviews the mechanisms of the impact of maternal childhood trauma on intergenerational transmission, providing insights for the prevention of intergenerational transmission of childhood trauma.

Virus-inspired strategies for cancer therapy.

The intentional use of viruses for cancer therapy dates back over a century. As viruses are inherently immunogenic and naturally optimized delivery vehicles, repurposing viruses for drug delivery, tumor antigen presentation, or selective replication in cancer cells represents a simple and elegant approach to cancer treatment. While early virotherapy was fraught with harsh side effects and low response rates, virus-based therapies have recently seen a resurgence due to newfound abilities to engineer and tune oncolytic viruses, virus-like particles, and virus-mimicking nanoparticles for improved safety and efficacy. However, despite their great potential, very few virus-based therapies have made it through clinical trials. In this review, we present an overview of virus-inspired approaches for cancer therapy, discuss engineering strategies to enhance their mechanisms of action, and highlight their application for overcoming the challenges of traditional cancer therapies.

High-resolution self-corrected single-pixel imaging through dynamic and complex scattering media.

Imaging with single-pixel detectors becomes attractive in many applications where pixelated detectors are not available or cannot work. Based on a correlation between the probing patterns and the realizations, optical imaging with single-pixel detector offers an indirect way to recover a sample. It is well recognized that single-pixel optical imaging through dynamic and complex scattering media is challenging, and dynamic scaling factors lead to serious mismatches between the probing patterns and the realizations. In this paper, we report self-corrected imaging to realize high-resolution object reconstruction through dynamic and complex scattering media using a parallel detection with dual single-pixel detectors. The proposed method can supervise and self-correct dynamic scaling factors, and can implement high-resolution object reconstruction through dynamic and complex scattering media where conventional methods could not work. Spatial resolution of 44.19 µm is achieved which approaches diffraction limit (40.0 µm) in the designed optical setup. The achievable spatial resolution is dependent on pixel size of spatial light modulator. It is experimentally validated that the proposed method shows unprecedented robustness against complex scattering. The proposed self-corrected imaging provides a solution for ghost recovery, enabling high-resolution object reconstruction in complex scattering environments.

High-fidelity and high-robustness free-space ghost transmission in complex media with coherent light source using physics-driven untrained neural network.

It is well recognized that it is challenging to realize high-fidelity and high-robustness ghost transmission through complex media in free space using coherent light source. In this paper, we report a new method to realize high-fidelity and high-robustness ghost transmission through complex media by generating random amplitude-only patterns as 2D information carriers using physics-driven untrained neural network (UNN). The random patterns are generated to encode analog signals (i.e., ghost) without any training datasets and labeled data, and are used as information carriers in a free-space optical channel. Coherent light source modulated by the random patterns propagates through complex media, and a single-pixel detector is utilized to collect light intensities at the receiving end. A series of optical experiments have been conducted to verify the proposed approach. Experimental results demonstrate that the proposed method can realize high-fidelity and high-robustness analog-signal (ghost) transmission in complex environments, e.g., around a corner, or dynamic and turbid water. The proposed approach using the designed physics-driven UNN could open an avenue for high-fidelity free-space ghost transmission through complex media.

High-fidelity ghost diffraction through complex scattering media using a modified Gerchberg-Saxton algorithm.

In this paper, we propose a modified Gerchberg-Saxton (GS) algorithm to generate random amplitude-only patterns as information carriers in ghost diffraction. With the generated random patterns, high-fidelity ghost diffraction through complex scattering media can be realized with a single-pixel detector. The modified GS algorithm adopts a support constraint in the image plane, which is divided into a target region and a support region. In the Fourier plane, amplitude of the Fourier spectrum is scaled to regulate the sum of the image function. A random amplitude-only pattern can be generated to encode a pixel of the data to be transmitted using the modified GS algorithm. Optical experiments are conducted to verify the proposed method in complex scattering environments, e.g., dynamic and turbid water with non-line-of-sight (NLOS). Experimental results demonstrate that the proposed ghost diffraction is of high fidelity and high robustness against complex scattering media. It is expected that an avenue could be opened up for ghost diffraction and transmission in complex media.

Optical analog-signal transmission system in a dynamic and complex scattering environment using binary encoding with a modified differential method.

High-fidelity optical transmission through dynamic scattering media is challenging, since transmission errors are induced due to dynamic scattering media. In this paper, a new scheme is proposed to realize high-fidelity free-space optical analog-signal transmission in dynamic and complex scattering environments using binary encoding with a modified differential method. Each pixel of an analog signal to be transmitted is first divided into two values, and each of them is encoded into a random matrix. Then, a modified error diffusion algorithm is utilized to transform the random matrix into a 2D binary array. Each pixel of the analog signal to be transmitted is eventually encoded into only two 2D binary arrays, and transmission errors and dynamic scaling factors induced by dynamic and complex scattering media can be temporally corrected. Dynamic smoke and non-line-of-sight (NLOS) are created as a dynamic and complex scattering environment to verify the proposed method. It is experimentally demonstrated that analog signals retrieved at the receiving end are always of high fidelity using the proposed method, when average path loss (APL) is less than 29.0 dB. Only the half number of measurements is used compared to that in conventional methods. The proposed method could open up a novel research perspective for high-fidelity free-space optical analog-signal transmission through dynamic and complex scattering media.

Securing 2D information carriers over dynamic and turbulent media in a free-space optical channel.

In this Letter, a new, to the best of our knowledge, scheme is proposed to realize high-fidelity secured free-space optical information transmission through dynamic and turbulent media by encoding 2D information carriers. The data are transformed into a series of 2D patterns as information carriers. A novel differential method is developed to suppress noise, and a series of random keys are also generated. A different number of absorptive filters are arbitrarily combined to be placed in the optical channel to generate ciphertext with high randomness. It is experimentally demonstrated that the plaintext can be retrieved only when correct security keys are applied. Experimental results demonstrate that the proposed method is feasible and effective. The proposed method provides an avenue for securing high-fidelity optical information transmission over dynamic and turbulent media in a free-space optical channel.

The deterioration of calcified cartilage integrity reflects the severity of osteoarthritis-A structural, molecular, and biochemical analysis.

The calcified cartilage zone (CCZ) is a thin interlayer between the hyaline articular cartilage and the subchondral bone and plays an important role in maintaining the joint homeostasis by providing biological and mechanical support from unmineralized cartilage to the underlying mineralized subchondral bone. The hallmark of CCZ characteristics in osteoarthritis (OA) is less well known. The aim of our study is to evaluate the structural, molecular, and biochemical composition of CCZ in tissues affected by primary knee OA and its relationship with disease severity. We collected osteochondral tissue samples stratified according to disease severity, from 16 knee OA patients who underwent knee replacement surgery. We also used meniscectomy-induced rat samples to confirm the pathophysiologic changes of human samples. We defined the characteristics of the calcified cartilage layer using a combination of morphological, biochemical, proteomic analyses on laser micro-dissected tissue. Our results demonstrated that the Calcium/Phosphate ratio is unchanged during the OA progression, but the calcium-binding protein and cadherin binding protein, as well as carbohydrate metabolism-related proteins, undergo significant changes. These changes were further accompanied by thinning of the CCZ, loss of collagen and proteoglycan content, the occurrence of the endochondral ossification, neovasculature, loss of the elastic module, loss of the collagen direction, and increase of the tortuosity indicating an altered structural and mechanical properties of the CCZ in OA. In conclusion, our results suggest that the calcified cartilage changes can reflect the disease progression.

Investigation of the chiral recognition role of cyclodextrin hydroxyl moieties via high performance liquid chromatography.

Cyclodextrin (CD) is known to afford excellent enantioselectivities due to its hydrophobic cavity and external H-bonding sites from hydroxyl moieties. However, there is still a lack of direct and comprehensive evidence clearly illustrating the origin of the important H-bonding effect. Regarding this issue, herein, four allylimidazole CD derivatives by selective substitution of the primary (6-position) and/or secondary (2,3-position) CD were synthesized and clicked onto silica surfaces to afford the corresponding chiral stationary phases (CSPs). The chiral chromatographic performances were systematically evaluated by separating 35 racemic analytes including isoxazolines, dansyl-amino acids, flavonoids and other racemates under reversed-phase HPLC. The chiral selection factors (α) and retention times (k) of the analytes on the as-prepared CSPs were comprehensively compared and it reveals that the enantioseparation ability was significantly altered due to the selective substituents of CD hydroxyl groups. The natural allylimidazole CD CSP (AICDCSP) was superior to the 6-O-tert-butyldimethylsilyl AICDCSP (6-TBDMAICDCSP) for most analytes. Dansyl amino acids and Ar-Pys were well separated on AICDCSP and 6-TBDMAICDCSP, where dansyl amino leucine gained the highest resolution up to 4.72 on AICDCSP, and flavonoids and Ar-Oprs were only separated on AICDCSP. These interesting separation results demonstrate that the secondary hydroxyl groups play a pivotal role in the separation of chiral compounds. In addition, the size of the CD cavity and the choice of solute also have an effect on the separation of substances. The mechanism involved in enantioselective discrimination of the selectively substituted CDs was further investigated by the molecular docking simulation.

Surface-up click access to allylimidazolium bridged cyclodextrin dimer phase for efficient enantioseparation.

In this work, a novel allylimidazolium-bridged bis(ß-cyclodextrin) chiral stationary phase was fabricated via a surface-up thiol-ene click chemistry reaction between 7-SH-ß-cyclodextrin and 1-allylimidazole-ß-cyclodextrin bonded on a silica surface. The structure of the allylimidazolium-bridged bis(ß-cyclodextrin) chiral stationary phase was characterized by Fourier transform infrared spectra, 13 C nuclear magnetic resonance, thermogravimetric analysis, and elemental analysis. Its chiral chromatographic performances were systematically evaluated by separating 35 racemic analytes including isoxazolines, dansyl-amino acids, and flavanones under reversed-phase high-performance liquid chromatography. Compared with the corresponding bottom and top layer of the ß-cyclodextrin stationary phase, the allylimidazolium-bridged bis(ß-cyclodextrin) chiral stationary phase afforded significantly accentuated chiral recognition ability due to its abundant hydrogen bond sites, electrostatic interactions, and synergistic inclusion. Furthermore, the allylimidazolium-bridged bis(ß-cyclodextrin) chiral stationary phase showed better enantioseparation ability compared to other reported bridged cyclodextrin stationary phases. In particular, Ar-Phs and dansyl-amino acid could be completely separated by allylimidazolium-bridged bis(ß-mono-6A -deoxy-6-allylimidazolium-ß-cyclodextrin chiral stationary phase) chiral stationary phase with high resolutions of 1.14-7.20 and 3.16-5.82, respectively. Molecular docking reveals that good enantioseparation ability arises from the different interaction modes and the synergistic effect of allylimidazolium-bridged bis(ß-cyclodextrin) chiral stationary phase.

Retracted: Effects of Different Ratio of n-6/n-3 Polyunsaturated Fatty Acids on the PI3K/Akt Pathway in Rats With Reflux Esophagitis.

This publication has been retracted by the Editor due to non-original content and deficiencies in the conduct of the study. Reference: Jia-Yuan Zhuang, Zhi-Yao Chen, Tao Zhang, Du-Peng Tang, Xiao-Yin Jiang, Ze-Hao Zhuang. Effects of Different Ratio of n-6/n-3 Polyunsaturated Fatty Acids on the PI3K/Akt Pathway in Rats with Reflux Esophagitis. Med Sci Monit, 2017; 23: 542-547. DOI: 10.12659/MSM.898131.

Roles of lncRNAs in pancreatic ductal adenocarcinoma: Diagnosis, treatment, and the development of drug resistance.

BACKGROUND: Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal cancers, primarily due to its late diagnosis, high propensity to metastasis, and the development of resistance to chemo-/radiotherapy. Accumulating evidence suggests that long non-coding RNAs (lncRNAs) are intimately involved in the treatment resistance of pancreatic cancer cells via interacting with critical signaling pathways and may serve as potential diagnostic/prognostic markers or therapeutic targets in PDAC. DATA SOURCES: We carried out a systematic review on lncRNAs-based research in the context of pancreatic cancer and presented an overview of the updated information regarding the molecular mechanisms underlying lncRNAs-modulated pancreatic cancer progression and drug resistance, together with their potential value in diagnosis, prognosis, and treatment of PDAC. Literature mining was performed in PubMed with the following keywords: long non-coding RNA, pancreatic ductal adenocarcinoma, pancreatic cancer up to January 2022. Publications relevant to the roles of lncRNAs in diagnosis, prognosis, drug resistance, and therapy of PDAC were collected and systematically reviewed. RESULTS: LncRNAs, such as HOTAIR, HOTTIP, and PVT1, play essential roles in regulating pancreatic cancer cell proliferation, invasion, migration, and drug resistance, thus may serve as potential diagnostic/prognostic markers or therapeutic targets in PDAC. They participate in tumorigenesis mainly by targeting miRNAs, interacting with signaling molecules, and involving in the epithelial-mesenchymal transition process. CONCLUSIONS: The functional lncRNAs play essential roles in pancreatic cancer cell proliferation, invasion, migration, and drug resistance and have potential values in diagnosis, prognostic prediction, and treatment of PDAC.