Migratory Properties Research Articles

Exploring the Role of Epithelial–Mesenchymal Transcriptional Factors Involved in Hematological Malignancy and Solid Tumors: A Systematic Review

Background: The epithelial mesenchymal transition (EMT) is a biological process in which epithelial cells lose their polarity and adhesion characteristics, and adopt a mesenchymal phenotype. While the EMT naturally occurs during tissue fibrosis, wound healing, and embryonic development, it can be exploited by cancer cells and is strongly associated with cancer stem cell formation, tissue invasiveness, apoptosis, and therapy resistance. Transcription factors (TFs) such as SNAIL, ZEB, and TWIST play a pivotal role in driving the EMT. This systematic review aims to assess the impact of EMT-TFs on hematological malignancy and solid tumors. Methods: English-language literature published between 2010 and 2024 was systematically reviewed, utilizing databases such as PubMed and Google Scholar. Results: A total of 3250 studies were extracted. Of these, 92 publications meeting the inclusion criteria were analyzed to elucidate the role of EMT-TFs in cancer. The results demonstrated that the EMT-TFs play a critical role in both hematological and solid tumor development and progression. They promote invasive, migratory, and metastatic properties in these tumors, and contribute to therapeutic challenges by enhancing chemoresistance. A strong correlation between EMT-TFs and poor overall survival has been identified. Conclusions: Our research concluded that EMT-TFs may serve as important predictive and prognostic factors, as well as potential therapeutic targets to mitigate cancer progression.

Use of deep eutectic solvents based on choline chloride, urea, and lactic acid as plasticizers in low‐density polyethylene films

AbstractThis study aims to investigate the performance of deep eutectic solvents (DESs) as plasticizers in low‐density polyethylene (LDPE) films and to compare them with di(2‐ethylhexyl) phthalate (DEHP). DESs were produced by mixing choline chloride with lactic acid and urea in 1:1 and 1:2 molar ratios. The prepared DESs were added to LDPE at two different ratios (10% and 30%), and films with 10 different compositions were produced by the extrusion method. The densities, viscosities, pH, volatility, and thermal values of the produced DESs were determined between 1.14 and 1.18 g/cm3, 22 and 99 mPa.s, 0.05 and 9.02, 0.7% and 18.9%, and <−70 and 63°C, respectively. When the DESs were examined in terms of their bond structure, it was observed that they could be produced successfully. The LDPE films with DES were characterized by thickness, mechanical, barrier, optical, DSC, FTIR, SEM, water behavior properties, heat sealability, and overall migration (OM) properties. According to the results of some basic analyses performed on the films, the first three films with the best properties (CL1:30, CL2:30, and DEHP:30) were determined using TOPSIS from the multi‐criteria decision hierarchy techniques. It was determined that the DES films with the most suitable properties had better properties than the control and DEHP films in terms of tensile strength (10–12 MPa), elongation at break (500%–545%), water vapor permeance (0.03–0.04 g/m2/h/kPa), and oxygen transmission rate (13–14 cm3/m2/day), water contact angle (>99°), and UV light barrier analyses. DES did not cause any change in the DSC and OM values of LDPE films. In general, important results were obtained regarding the use of DES as effective plasticizers in LDPE films.Highlights DES is a sustainable alternative to DEHP for LDPE plasticization. DES‐plasticized films showed 400% better elongation performance. DES‐plasticized films showed 25% better water vapor and 80% better oxygen barriers. DES‐plasticized films have superior UV light barrier and hydrophobic properties. DES‐plasticized films did not affect thermal stability or OM.

Cyanidin-3-glucoside reduces cell migration and inflammatory profile of acute leukemia cells.

Anthocyanins, water-soluble flavonoids found in fruits and vegetables, exhibit diverse biological activities, with cyanidin being the most common pigment. While cyanidin's chemo preventive and -antioxidant activity is well-studied, its impact on inflammatory profile and migration capacity of leukemic cells are less understood. This study evaluates the effects of Cyanidin-3-glucoside (C3G) on the inflammatory mechanisms influencing leukemic cell migration. Results show that C3G doses up to 50 µM do not affect cell metabolism, viability, or cell cycle phases. C3G significantly reduces TNF-α, IL-8, CCL2 production, and the p-NFκB/NFκB ratio in LPS (Lipopolysaccharide)-challenged cells. It also diminishes migration rates in response to LPS or fMLP (N-formyl-methionyl-leucyl-phenylalanine) stimulation and reduces Rho-GTP expression. Thus, C3G modifies the inflammatory and migration properties of leukemic cells, highlighting the potential of anthocyanins as a complementary therapy and an avenue for further therapeutic intervention.

Cell fusion as a driver of metastasis: re-evaluating an old hypothesis in the age of cancer heterogeneity

Numerous studies have investigated the molecular mechanisms and signalling pathways underlying cancer metastasis, as there is still no effective treatment for this terminal stage of the disease. However, the exact processes that enable primary cancer cells to acquire a metastatic phenotype remain unclear. Increasing attention has been focused on the fusion of cancer cells with myeloid cells, a phenomenon that may result in hybrid cells, so-called Tumour Hybrid Cells (THCs), with enhanced migratory, angiogenic, immune evasion, colonisation, and metastatic properties. This process has been shown to potentially drive tumour progression, drug resistance, and cancer recurrence. In this review, we explore the potential mechanisms that govern cancer cell fusion, the molecular mediators involved, the metastatic characteristics acquired by fusion-derived hybrids, and their clinical significance in human cancer. Additionally, we discuss emerging pharmacological strategies aimed at targeting fusogenic molecules as a means to prevent metastatic dissemination.

Synthesis mechanisms, property characterization, and environmental applications of biogenic FeS: A review.

Iron sulfide (FeS) exhibits superior reactivity toward a wide range of contaminants, making it a promising candidate for environmental remediation in various media, including surface water, wastewater, soil, and groundwater. Driven by green and sustainable development principles, efficient, low-cost, and environmentally friendly biosynthesis has attracted considerable attention and has great environmental remediation potential. This review provides a comprehensive overview of the recent advances in biogenic FeS (bio-FeS), focusing on its synthesis mechanisms, performance characterization, and environmental applications. To the best of our knowledge, this is the first review exclusively dedicated to this emerging field. This review begins with an in-depth description of the four bio-FeS biosynthetic pathways, the primary actors of which are sulfate-reducing bacteria (SRB), iron-reducing bacteria (IRB), coupled SRB and IRB, and bio-extracts. Notably, SRB account for approximately half of the bio-FeS synthesis. Various characterization techniques, including scanning electron microscopy, X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, Raman spectroscopy, Fourier transform infrared spectroscopy, and Brunauer-Emmett-Teller analysis, have been discussed in depth to better understand the structure and properties of bio-FeS. In terms of morphological structure, the bio-FeS synthesized by SRB exhibited primarily flakes (similar to mackinawite), whereas the bio-FeS synthesized by IRB was chiefly spherical. Bio-FeS transportation, migration, and permeation properties were also explored. Furthermore, bio-FeS application in the removal of various contaminants, including arsenic, chromium, uranium, complex pollutants, rare earth elements, chlorinated hydrocarbons, and antibiotics, and their underlying mechanisms were discussed. Finally, the challenges and future research directions related to bio-FeS environmental applications were discussed. This review aims to provide valuable insights into bio-FeS synthesis and environmental applications, thereby supporting the development of innovative and sustainable technologies for environmental remediation.

Thermosensitive-based synergistic antibacterial effects of novel LL37@ZPF-2 loaded poloxamer hydrogel for infected skin wound healing.

Trauma healing is the process of healing after the body has been subjected to an external force and the skin and other tissues have become dissected or defective, showing the synergistic effect of various processes. Therefore, the investigation of innovative wound dressings has significant research and clinical implications. In this study, we constructed a zinc based metal-organic framework (MOF) and loaded with antimicrobial peptide LL37 to prepare LL37@ZPF-2 (ZPF = zeolite pyrimidine backbone), which was subsequently integrated with Poloxamer 407 to fabricate LL37@ZPF-2 thermosensitive hydrogel. Our study showed that in-situ packaging method can achieve encapsulation rate of 98 % and 15 % of drug loading for LL37. LL37@ZPF-2 demonstrated a higher inhibitory potency against S.aureus compared to E.coli. The Poloxamer 407-gel exhibits thermo-responsive sol-to-gel phase transition behaviors with a phase transition temperature (Tsol/gel) of ∼ 28.01℃, making it an appropriate material for wound healing. The composite hydrogel has excellent biocompatibility and hemocompatibility. A full-thickness skin defect model was built to confirm that LL37@ZPF-2 thermosensitive hydrogel dressing could inhibit bacterial growth, reduce the risk of wound infection, and stimulate angiogenesis and collagen deposition, resulting in a wound healing rate of 94.4 % on day 7 and complete healing on day 10. Our findings demonstrate that the novel thermosensitive LL37@ZPF-2 hydrogel confers good antibacterial activity, promoting cell migration and infected-wound healing properties, providing a promising platform for wound healing.

Spatial transcriptomics reveals cancer and stromal cell heterogeneity between center and invasive front of pancreatic cancer.

Intratumor heterogeneity is considered a major cause of treatment failure in pancreatic ductal adenocarcinoma (PDAC). In recent years, marked heterogeneity at the genomic and transcriptional level has been revealed, but the spatial distribution of the heterogeneous cell populations has not been considered. Yet, it is assumed that cancer cells at the invasive front are endowed with enhanced migratory and invasive properties, although evidence is scanty, and cancer-associated fibroblasts (CAFs) in this location have not been characterized. In this study, digital spatial profiling was used to compare the transcriptional profiles of cancer cells and CAFs in the tumor center versus the invasive front of human PDAC. Four well differentiated PDACs with conventional morphology were investigated with the GeoMx system (Nanostring). Regions of interest were analyzed in the tumor center and at the invasive front using a whole transcriptome assay in cancer cell and CAF segments separately. Three of the PDACs harbored mutated KRAS, while the fourth case was confirmed wild-type KRAS. Substantial inter-regional heterogeneity was identified, with increased activity of pathways associated with cellular stress (including TNFα-signaling via NFκB, hypoxia, P53 pathway), proliferation (MYC targets, mitotic spindle), glycolysis, and epithelial-mesenchymal transition at the invasive front in both the cancer cell and CAF segments compared to the center of the tumor. Immunohistochemical validation on 17 PDACs of well, moderate and poor differentiation confirmed significant inter-regional heterogeneity in the expression level of markers of EMT and glycolysis. The results of this study show that in PDAC, transcriptional profiles of both cancer cells and CAFs differ between the center of the tumor and the invasive front.

Canid alphaherpesvirus 1 infection alters the gene expression and secretome profile of canine adipose-derived mesenchymal stem cells in vitro

BackgroundCanine adipose-derived mesenchymal stem cells (cAD-MSCs) demonstrate promising tissue repair and regeneration capabilities. However, the procurement and preservation of these cells or their secreted factors for therapeutic applications pose a risk of viral contamination, and the consequences for cAD-MSCs remain unexplored. Consequently, this research sought to assess the impact of canid alphaherpesvirus 1 (CHV) on the functional attributes of cAD-MSCs, including gene expression profiles and secretome composition.MethodsTo this end, abdominal adipose tissue from 12 healthy dogs was harvested to isolate cAD-MSCs. These samples were tested for CHV contamination before introducing a wild-type CHV strain via serial passages. Following CHV infection, real-time reverse transcription-polymerase chain reaction array and liquid chromatography with tandem mass spectrometry assessments enabled analyses of gene expression and secretome’s proteomic profile, respectively.ResultsThis study showed that the initial cAD-MSC populations were devoid of CHV. cAD-MSCs showed susceptibility to infection with wild-type CHV, leading to notable modifications in gene expression and secretome profile. The observed genomic variations in gene expression indicate potential impacts on the stemness, migration, and other functional properties of cAD-MSCs, highlighting the need for further studies to evaluate their functional capacity post-infection. Moreover, gene expression and secretome analyses suggest a shift in stem cell differentiation toward an adipogenic phenotype.ConclusionTo the best of our knowledge, this is the first study of the effects of virus infection on gene expression and secretome composition in cAD-MSCs. The outcomes of our study underscore the imperative of routine viral screening prior to the therapeutic use of cAD-MSCs. Moreover, these findings provide novel insights into the pathogenic mechanisms of CHV and pave the way for future canine stem cell and virus research.

The Impact of Carbon on Electronic Structure of N-Doped ZnO Films: Scanning Photoelectron Microscopy Study and DFT Calculations.

A Scanning Photoelectron Microscopy (SPEM) experiment has been applied to ZnO:N films deposited by Atomic Layer Deposition (ALD) under O-rich conditions and post-growth annealed in oxygen at 800 °C. State-of-the-Art spatial resolution (130 nm) allows for probing the electronic structure of single column of growth. The samples were cleaved under ultra-high vacuum (UHV) conditions to open atomically clean cross-sectional areas for SPEM experiment. It has been shown that different columns reveal considerably different shape of the valence band (VB) photoemission spectra and that some of them are shifted towards the bandgap. The shift of the VB maximum, which is associated with hybridization with acceptor states, was found to be correlated with carbon content measured as a relative intensity of the C1s and Zn3d core levels. Generalized Gradient Approximation (GGA) supplemented by +U correction was applied to both Zn3d and O2p orbitals for calculation of the VZn migration properties by the Nudged Elastic Band (NEB) method. The results suggest that interstitial -CHx groups facilitate the formation of acceptor complexes due to additional lattice perturbation.

Carvacrol is a Novel Natural Therapeutic Approach Through the Inhibition of Proliferation, Autophagy and Migration in Pancreatic Ductal Adenocarcinoma Cells

Objective: Pancreatic ductal adenocarcinoma, which is the most common and aggressive pancreatic cancer, has the highest mortality rate of cancers because of difficulties in diagnosis and chemoresistance. As the chemotherapeutic options are very limited and insufficient for PDAC, novel effective therapeutic approaches are urgently needed for pancreatic cancer patients. Carvacrol naturally found in thyme (Thymus vulgaris), wild bergamot (Citrus aurantium var. bergamia Loisel), black cumin (Nigella sativa), marjoram (Origanum scabrum, Origanum microphyllum, Origanum onites, Origanum vulgare) and black pepper (Lepidium flavum) plants is shown to have antibacterial and antioxidant effects. In this study, we aimed to investigate the anticarcinogenic potential of carvacrol through proliferation and autophagy in PDAC cells. Material and Method: To determine the anti-proliferative effects of carvacrol in Panc-1 cells, we performed the MTS assay using different carvacrol doses of 100, 200, 300, 400, 500, 600, 700 and 800 μM at 24h, 48h, 72h. The gene and protein expressions of Atg16L1 and Beclin-1, autophagy key mediators, were analyzed by RT-PCR and western blot in Panc-1 cells treated with 300 and 400 μM for 24h, 48h. Additionally, the migrative property of PDAC cells was evaluated using a wound healing assay. Results: Based on MTS results, carvacrol significantly inhibited cell proliferation in the doses of 300 and 400 μM at 24h and 48 h in Panc-1. These same doses led to decreased autophagy and migration through Atg16L1, and Beclin-1 expressions. Conclusion: Our findings first revealed that carvacrol has promising value as a potential therapeutic approach for PDAC. We believe that further mechanistic investigations will be a guide for its clinical usage.

Solution Process–Based Facile Flame–Boosted Low‐Valence Transition Metal Doping on Pristine Oxide for Highly Enhanced Photoelectrochemical Solar Water Oxidation Reaction

ABSTRACTAs for the high sustainable solar hydrogen production via water splitting, transition metal doping on an oxide photoanode in photoelectrochemical (PEC) cells has been recognized as an effective approach. However, conventional thermal‐diffusion‐mediated doping strategies face the challenge of resolving sluggish catalytic kinetics for oxygen evolution reaction (OER) and its practical utilization for the synthesis of photoanode films. Herein, we introduce facile ultrafast flame‐boosted doping of Mo into a BiVO4 (FL MoBVO) film for 20 s to achieve an efficient PEC OER. Mo elements in a low‐valence state (i.e., Mo6−δ) and Mo6+ are successfully doped into the photoanode, which manipulate the energy band structure, facilitating the downward shift of band edges and promoting the surface catalytic kinetics. Consequently, the flame‐boosted Mo‐doping results in superior PEC performance in a mild environment with neutral electrolyte without introducing any other additives or co‐catalysts, where the photocurrent density at 1.23 VRHE under 1 sun illumination in pH 7 is outstandingly enhanced, over 9‐fold higher than that of a pristine BiVO4. The flame‐boosted doping induces significantly enhanced photoexcited charge transport and catalytic reaction kinetics performances simultaneously. Our report provides the effective strategy boosting both the thermodynamic and kinetic charge migration properties for sustainable materials.

Decoding the role of SLC25A5 in osteosarcoma drug resistance and CD8+ T cell exhaustion: The therapeutic potential of phyllanthin.

Osteosarcoma is an aggressive malignant bone tumor with an obscure etiology, as well as high prevalence and poor prognosis in children and adolescents. We aimed to investigate the pathogenesis of osteosarcoma through a comprehensive analysis of the tumor immune microenvironment (TIME) using multiple single-cell RNA sequencing datasets. SLC25A5, a gene implicated in cellular aging, significantly influenced osteosarcoma development by altering the TIME and promoting CD8+ T cell exhaustion, which contributed to reduced chemosensitivity. Experimental validation demonstrated that SLC25A5 enhanced the proliferative, migratory, invasive, and osteolytic properties of drug-resistant osteosarcoma cells while reducing apoptosis, intensifying cisplatin resistance. Phyllanthin inhibited the malignant phenotype of cisplatin-resistant osteosarcoma cells and enhanced their sensitivity to cisplatin by suppressing SLC25A5 expression. This study highlights a novel pathogenic role of SLC25A5 in osteosarcoma and presents Phyllanthin as a promising therapeutic agent. Our study offers a pioneering exploration of the single-cell spatiotemporal evolution of osteosarcoma and identifies SLC25A5 as a critical factor in drug resistance and immune evasion. By integrating advanced single-cell technologies and functional assays, we provided novel insights into the molecular mechanisms underlying osteosarcoma progression and treatment resistance, facilitating innovative therapeutic strategies.

Effect of combination of polyphenols, polysaccharide, and sodium selenite on bortezomib anti-cancer action.

Combinatorial drug delivery has shown promising results over single drug for cancer therapy. Here, we aimed to explore combination of proteasome inhibitor; bortezomib (BTZ) with natural antioxidants (AOs); polyphenols like caffeic acid (CFA), resveratrol (RES), fucoidan (FD), and synthetic AO; sodium selenite (Na2SeO3) for cellular cytotoxicity in breast cancer cell lines; MCF-7 and MDA MB-231. The combination of RES + BTZ, FD + BTZ, and Na2SeO3 + BTZ showed synergism while CFA showed antagonism with BTZ. The EC50 values of different combinations were found to be significantly less than the individual AOs in ABTS and DPPH assay. Furthermore, the effect of combination of drugs on migratory properties of MCF-7 cells were evaluated by in-vitro wound healing assay, resulting in the reduction of such behavior. In support of this, RT-qPCR was performed to analyze differential gene expressions of apoptotic and Epithelial-Mesenchymal Transition (EMT) markers with and without treatment. In results, the combination of Na2SeO3 + BTZ reduced the expression of Bcl-XL and N-Cad causing cytotoxicity and suggested that the combination of Na2SeO3 + BTZ (IC50 = 1.40 ± 0.45 μM) could be a better option among other combinations for breast cancer therapy. Overall, the outcome indicates that the combination of BTZ with AOs may yield potential therapeutic benefit.

Anti-migration of DOS by Using HTPB/GO liner and GO film

Abstract The enhancement of anti-migration performance in insulation materials is critical for the stability and reliability of solid rocket motors (SRMs). This study explores two innovative methods to improve the barrier properties of Ethylene Propylene Diene Monomer (EPDM) insulation layers. Firstly, a composite liner combining Hydroxyl-Terminated Polybutadiene (HTPB) and Graphene Oxide (GO) was synthesized through a solution blending method. Additionally, a GO film was fabricated and integrated with the HTPB liner and EPDM to create a multilayer sandwich structure. The incorporation of these materials was found to significantly enhance the anti-migration performance, with the composite samples showing a 16.89% improvement over standard samples. The layered structure of GO effectively impedes the migration of dioctyl sebacate (DOS), enhancing the anti-plasticizer migration properties of the EPDM. While the multilayer sandwich samples also demonstrated improved performance, issues with adhesion between the GO film and EPDM lead to reduce its effectiveness. Future research will focus on improving the adhesion between the GO film and EPDM to further enhance anti-migration performance. This study provides valuable insights for developing high-performance EPDM insulation materials with enhanced anti-migration properties for aerospace applications.

Neurotensin Conjugated Polymeric Porous Microparticles Suppress Inflammation and Improve Angiogenesis Aiding in Diabetic Wound Healing.

Neurotensin (NT), a bioactive tridecapeptide aids in diabetic wound healing by modulating inflammation and angiogenesis. However, its rapid degradation in peptidase-rich wound environment (plasma half-life <2 min) limits its efficacy. To address this, neurotensin-conjugated polymeric porous microparticles (NT-PMP) were developed and loaded in gelatin (hydrogel 15% w/v) for topical application, enabling sustained NT release to enhance therapeutic outcomes. NT-PMP exhibited a size range of 60 - 240 µm (mean: 120.63 ± 40.71 µm) and pore size of 5 - 16 µm (average: 10.68 ± 3.47 µm). In vitro studies demonstrated cytocompatibility of NT-PMP in fibroblasts and reduced TNF-α levels in inflammation-induced macrophages (1256 ± 167.02 pg/ml). Further NT-PMP scaffold depicted excellent cell adhesion and migration properties upon seeding of dermal fibroblasts on surface of PMPs. In vivo studies in diabetic wound rat model demonstrated effective wound management, characterized by notable regenerative and healing attributes in the presence of NT-PMP. This included complete re-epithelialization, reducing pro-inflammatory cytokine (TNF-α), and enhancing VEGF expression, ultimately leading to the development of a well-organized collagen matrix in diabetic wounds upon application of NT-PMP gel.Altogether, NT conjugated PMP loaded in hydrogel demonstrated significant regenerative and healing properties, suggesting its potential as an alternative treatment for diabetic wounds.

Potential Use of Exosomal Non-Coding MicroRNAs in Leukemia Therapy: A Systematic Review.

Leukemia is a heterogeneous group of hematological malignancies. Despite the enormous progress that has been made in the field of hemato-oncology in recent years, there are still many problems related to, among others, disease recurrence and drug resistance, which is why the search for ideal biomarkers with high clinical utility continues. Research shows that exosomes play a critical role in the biology of leukemia and are associated with the drug resistance, metastasis, and immune status of leukemias. Exosomes with their cargo of non-coding RNAs act as a kind of intermediary in intercellular communication and, at the same time, have the ability to manipulate the cell microenvironment and influence the reaction, proliferative, angiogenic, and migratory properties of cells. Exosomal ncRNAs (in particular, circRNAs and microRNAs) appear to be promising cell-free biomarkers for diagnostic, prognostic, and treatment monitoring of leukemias. This review examines the expression of exosomal ncRNAs in leukemias and their potential regulatory role in leukemia therapy but also in conditions such as disease relapse, drug resistance, metastasis, and immune status. Given the key role of ncRNAs in regulating gene networks and intracellular pathways through their ability to interact with DNA, transcripts, and proteins and identifying their specific target genes, defining potential functions and therapeutic strategies will provide valuable information.

Novel flexible and active expanded-starch films enriched with Agrifood waste via microwave irradiation

Expanded materials possess valuable properties for food packaging, including thermal insulation and lightweight. However, developing sustainable alternatives with the potential to replace lightweight petroleum-based plastics is highly challenging. Starch biopolymer is a promising sustainable candidate due to its compostable character, great foamability and processability. Moreover, its chemical characteristics allow its combination with agrifood wastes to promote the circular economy and provide active properties. Most of the starch foams reported with low density are processed via extrusion and they are notably brittle and rigid, restricting their application. In this work, different expanded starch biocomposites, without or enriched with 40 wt.% orange peel (OP), were fabricated using 30 s of microwave (MW) irradiation, acquiring different properties depending on the main blowing agent used (i.e., water, sodium bicarbonate or expandable microspheres). These samples were fully characterized in terms of morphology, density, expansion degree, water uptake and solubility, mechanical properties, migration and antioxidant properties. Remarkably, the final expanded materials reached a considerably low density of 0.3 g/cm3 and they exhibited exceptional flexibility, overcoming the important drawback of starch foams. Finally, the benefits of adding 40 wt.% of agrifood waste were not only environmental, but OP increased the expansion capacity and gave outstanding antioxidant properties.

Exploring mesenchymal stem cells homing mechanisms and improvement strategies.

Mesenchymal stem cells (MSCs) are multipotent cells with high self-renewal and multilineage differentiation abilities, playing an important role in tissue healing. Recent advancements in stem cell-based technologies have offered new and promising therapeutic options in regenerative medicine. Upon tissue damage, MSCs are immediately mobilized from the bone marrow and move to the injury site via blood circulation. Notably, allogenically transplanted MSCs can also home to the damaged tissue site. Therefore, MSCs hold great therapeutic potential for curing various diseases. However, one major obstacle to this approach is attracting MSCs specifically to the injury site following systemic administration. In this review, we describe the molecular pathways governing the homing mechanism of MSCs and various strategies for improving this process, including targeted stem cell administration, target tissue modification, in vitro priming, cell surface engineering, genetic modifications, and magnetic guidance. These strategies are crucial for directing MSCs precisely to the injury site and, consequently, enhancing their migration and local tissue repair properties. Specifically, our review provides a guide to improving the therapeutic efficacy of clinical applications of MSCs through optimized in vivo administration and homing capacities.

Potassium and Boron Co-Doping of g-C3N4 Tuned CO2 Reduction Mechanism for Enhanced Photocatalytic Performance: A First-Principles Investigation.

Graphitic phase carbon nitride (g-C3N4, abbreviated as CN) can be used as a photocatalyst to reduce the concentration of atmospheric carbon dioxide. However, there is still potential for improvement in the small band gap and carrier migration properties of intrinsic materials. K-B co-doped CN (KBCN) was investigated as a promising photocatalyst for carbon dioxide reduction via the Density Functional Theory (DFT) method. The electronic and optical properties of CN and KBCN indicate that doping K and B can improve the catalytic performance of CN by promoting charge migration and separation. In terms of the Gibbs free energy change, the CO2 reduction reaction catalysed by KBCN results in CH3OH, and its optimal pathway is CO2 → *CO2 → *COOH → CO → *OCH → HCHO → *OCH3 → CH3OH. Compared with CN, the doping elements K and B shift the rate-determining step from CO2 → *CO2 to *CO2 → *COOH. The K and B elements co-doping tuned the charge distribution between the catalyst and the adsorbate and reduced the Gibbs free energy of the rate-determining step from 1.571 to 0.861 eV, suggesting that the CO2 reduction activity of KBCN is superior to that of CN. Our work provides useful insights for the design of metallic-nonmetallic co-doped CN for photocatalytic CO2 reduction (CO2PR) reactions.

HERV-W envelope protein is present in microglial cells of the human glioma tumor microenvironment and differentially modulates neoplastic cell behavior

Gliomas are the most common parenchymal tumors of the central nervous system (CNS). With regard to their still unclear etiology, several recent studies have provided evidence of a new category of pathogenic elements called human endogenous retroviruses (HERVs) which seem to contribute to the evolution and progression of many neurological diseases such as amyotrophic lateral sclerosis (ALS), schizophrenia, chronic inflammatory polyneuropathy (CIDP) and, particularly, multiple sclerosis (MS). In these diseases, HERVs exert effects on cellular processes such as inflammation, proliferation, and migration. In previous studies, we demonstrated that in MS, the human endogenous retrovirus type-W envelope protein (HERV-W ENV) interferes with lesion repair through the activation of microglia (MG), the innate myeloid immune cells of the CNS. Here, we now show that HERV-W ENV is also present in the microglial cells (MG) of the tumor microenvironment (TME) in gliomas. It modulates the behavior of glioblastoma (GBM) cell lines in GBM/MG cocultures by altering their gene expression, secreted cytokines, morphology, proliferation, and migration properties and could thereby contribute to key tumor properties.