Adhesion Of Cells Research Articles

Ethyl pyruvate attenuates cellular adhesion and proliferation of diffuse large B-cell lymphoma by targeting c-Jun.

Diffuse large B-cell lymphoma (DLBCL) stands out as the most common type of malignant cancer, representing the majority of cases of non-Hodgkin's lymphoma. Ethyl pyruvate (EP) is a derivative of pyruvic acid and found to have potent anti-tumor properties. Despite its potential benefits, the impact of EP on DLBCL remains ambiguous. Our objective is to elucidate the role of EP in modulating the development of DLBCL. Analysis of cholecystokinin-8 (CCK-8) revealed that treatment with EP significantly diminished the viability of DLBCL cells. Furthermore, EP administration suppressed colony formation and hindered cell adhesion and invasion in DLBCL cells. Examination of cell cycle progression showed that EP treatment induced arrest at the G1 phase and subsequently reduced the S phase population in DLBCL cells. EP treatment consistently exhibited apoptosis-inducing properties in Annexin-V assays, and notably downregulated the expression of Bcl-2 while increasing levels of proapoptotic cleaved caspase 3 and BAX in DLBCL cells. Additionally, EP treatment decreased the overexpression of c-Jun in c-Jun-transfected DLBCL cells. Further, EP demonstrated DNA-damaging effects in TUNEL assays. In vivo, xenograft animal models revealed that EP treatment significantly mitigated DLBCL tumor growth and suppressed DLBCL cell adhesion to bone marrow stromal cells. In summary, these findings suggest that EP mitigates DLBCL progression by inducing apoptosis, inducing cell cycle arrest, and promoting DNA damage.

Modification of The Bacterial Abundance Properties of Water by Immersed Non-Activated Charcoal

The present studies aim at reducing the planktonic bacterial load in drinking water using non-activated charcoal. The evaluation is dependent on the incubation time and the different physiological states of the bacterial cells. Three bacteria (Vibrio cholerae, Escherichia coli and Staphylococcus aureus) and two charcoal substrates (Okan and Tali) were used for the experimentation. The Bacteria adhered to charcoal fragments in varying degrees. Overall, the concentrations of fixed Vibrio cholerae reached 53.4x107 CFU/cm2 and 39.6x107 CFU/cm2 after 9 hours of contact in exponential phase on the Okan and Tali respectively. Those of fixed Staphylococcus aureus reached 5.8x106 CFU/cm2 after 3 hours of contact in exponential phase and 3.4x106 CFU/cm2 after 3 and 6 hours of contact in the same phase, on the Okan and the Tali, respectively. The highest abundances of Escherichia coli adhered to the charcoal fragments were 50.4x107 CFU/cm² on Okan and 53.2x107 CFU/cm² on Tali after 9 hours of contact in the exponential phase. The highest adsorption coefficient (639.06 adhered cells/cm2) was noted on Okan in the exponential phase with Vibrio cholerae cells; and the lowest (1.02 adhered cells/cm2) on Tali in stationary phase with Staphylococcus aureus. The incubation time significantly (P<0.01) influenced the adhesion of bacterial cells to charcoal substrates. Although the adsorption capacity and intensity of Okan were relatively higher, the comparison of the adsorption potential of the two substrates considered did not reveal any significant difference (P>0.05), reflecting the absence of the influence of the physical properties of these substrates on cell retention.

Role of ICAM1 on Immune Cells in Glioblastoma: A Review Study

Introduction: Glioblastoma, also known as glioblastoma multiforme (GBM), is a highly aggressive and incurable form of brain tumor that grows rapidly. Intracellular cell adhesion molecule 1 (ICAM1) is a glycoprotein and adhesion receptor that plays a multifaceted role in immune response and can serve as a therapeutic target. Due to the severity and poor prognosis associated with GBM, the interaction between ICAM1 and GBM has been a topic of interest in the hope of providing therapeutic value. Methods: This review synthesizes existing literature and studies through searches in the PubMed, Google Scholar, Web of Science, Ovid-Medline, and EBSCO databases to explore the role of ICAM1 on immune cells in the context of GBM. Search terms such as “GBM,” “ICAM1,” “tumor microenvironment,” as well as “adhesion molecules” and “GBM treatment” were employed. Literature was selected based on its applicability to key aspects of the research topic. Results: This comprehensive review anticipated uncovering the complex role of ICAM1 in immune cell adhesion in GBM. By promoting the adhesion of immune cells, such as T lymphocytes and natural killer cells, ICAM1 can potentially enhance the body's natural defense mechanisms against GBM. However, the tumor microenvironment (and interaction with other molecules) can also manipulate and alter ICAM1 in ways that inhibits an effective immune response, potentially resulting in tumor progression. Discussion: Understanding the role of ICAM1 in GBM can present new strategies for immune-based therapies in GBM, potentially leading to improved treatment outcomes. Moreover, gaining insight into how adhesion molecules, such as ICAM1, respond to the tumor microenvironment can advance GBM therapy and also provide insights into treatment options for various cancers. Conclusion: ICAM1 exerts both pro-tumorigenic and anti-tumorigenic effects, shaping tumor progression and immune evasion. Understanding these dual roles can guide the development of targeted therapies for GBM.

In vitro investigations on interference of selected probiotic candidates with Campylobacter jejuni adhesion and invasion of primary chicken derived cecal and Caco-2 cells

BackgroundCampylobacter (C.) jejuni is one of the most important bacterial foodborne pathogens worldwide. Probiotics such as Lactobacillus or Bacillus species are considered one option for reducing the colonization rate and magnitude in poultry, the most frequent source of human infections. Due to the lack of suitable avian in vitro models such as chicken intestinal cell lines, especially those derived from the cecum, most in vitro studies on C. jejuni host interaction have been conducted with human intestinal cell lines. In this study, we compared C. jejuni-cell interactions between primary chicken cecal cells and the human intestinal cell line Caco-2, which is derived from colorectal adenocarcinoma, and investigated possible interfering effects of selected probiotic candidates.ResultsWe detected differences in adhesion and invasion between the two tested gut cell types and between different C. jejuni strains. The probiotic inhibition of C. jejuni adhesion and invasion of human and avian gut cells was affected by host cell type, investigated C. jejuni strain and time points of probiotic treatment. Additionally, our results suggest a possible correlation between C. jejuni invasion and the detected increase in IL-6 mRNA expression.ConclusionsOur results indicate distinct differences between avian and human gut cells in their interaction with C. jejuni. Therefore, data obtained in one host species on C. jejuni-host interaction may not easily be transferrable to another one. The factors influencing the variable efficacy of probiotic intervention in chicken and human derived cells should be investigated further.

Sulfonamide-chalcone hybrid compound suppresses cellular adhesion and migration: Experimental and computational insight

In the present study, the effect of sulfonamide-chalcone 185 (SSC185) was investigated against B16–F10 metastatic melanoma cells aggressive actions, besides migration and adhesion processes, by in silico and in vitro assays. In silico studies were used to characterize the pharmacokinetic profile and possible targets of SSC185, using the pkCSM web server, and docking simulations with AutoDock Tools. Furthermore, the antimetastatic effect of SSC185 was investigated by in vitro experiments using MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide), colony, scratch, and cell adhesion assays, and atomic force microscopy (AFM). The molecular docking results show better affinity of SSC185 with the metalloproteinases-2 (MMP-2) and α5β1 integrin. SSC185 effectively restricts the formation of colonies, migration, and adhesion of B16–F10 metastatic melanoma cells. Through the AFM images changes in cells morphology was identified, with a decrease in the filopodia and increase in the average cellular roughness. The results obtained demonstrate the potential of this molecule in inhibit the primordial steps for metastasis, which is responsible for a worse prognosis of late stage cancer, being the main cause of morbidity among cancer patients.

Biocompatibility characterisation of CMOS-based Lab-on-Chip electrochemical sensors for in vitro cancer cell culture applications

Lab-on-Chip electrochemical sensors, such as Ion-Sensitive Field-Effect Transistors (ISFETs), are being developed for use in point-of-care diagnostics, such as pH detection of tumour microenvironments, due to their integration with standard Complementary Metal Oxide Semiconductor (CMOS) technology. With this approach, the passivation of the CMOS process is used as a sensing layer to minimise post-processing, and Silicon Nitride (Si3N4) is the most common material at the microchip surface. ISFETs have the potential to be used for cell-based assays however, there is a poor understanding of the biocompatibility of microchip surfaces. Here, we quantitatively evaluated cell adhesion, morphogenesis, proliferation and mechano-responsiveness of both normal and cancer cells cultured on a Si3N4, sensor surface. We demonstrate that both normal and cancer cell adhesion decreased on Si3N4. Activation of the mechano-responsive transcription regulators, YAP/TAZ, are significantly decreased in cancer cells on Si3N4 in comparison to standard cell culture plastic, whilst proliferation marker, Ki67, expression markedly increased. Non-tumorigenic cells on chip showed less sensitivity to culture on Si3N4 than cancer cells. Treatment with extracellular matrix components increased cell adhesion in normal and cancer cell cultures, surpassing the adhesiveness of plastic alone. Moreover, poly-l-ornithine and laminin treatment restored YAP/TAZ levels in both non-tumorigenic and cancer cells to levels comparable to those observed on plastic. Thus, engineering the electrochemical sensor surface with treatments will provide a more physiologically relevant environment for future cell-based assay development on chip.

Cytotoxicity of Polymer Scaffolds Suitable for Manufacturing of Small-Diameter Vascular Grafts

Aim.To evaluate the cytotoxicity of poly(ε-caprolactone) and polyurethane scaffolds in vitro.Materials and Methods. Polymer scaffolds were made by electrospinning from a 12% solution of poly(ε-caprolactone) or a 12% solution of polyurethane. Surface structure was examined by scanning electron microscopy, whilst cytotoxicity was evaluated by seeding EA.hy 926 endothelial cells on scaffold surface for 72 hours. Cell culture viability and proliferation was assessed by MTT assay and by quantifying cell culture density. On the xCELLigence device, cells were cultured in the presence of the studied matrix samples, and the dynamics of cell culture growth was evaluated in real time.Results. Poly(ε-caprolactone) scaffolds were characterised by a higher variability in the filament thickness and by a significantly larger pore size. Polyurethane filaments formed a dense web with a smoother surface. Poly(ε-caprolactone) scaffolds had significantly higher biocompatibility in comparison with polyurethane. Adhesion of cells to poly(ε-caprolactone) scaffolds did not differ from the cell culture plastic, and poly(ε-caprolactone) supported cell proliferation in the MTT test. Poly(ε-caprolactone) and polyurethane did not differ significantly in terms of inducing cell proliferation. Both poly(ε-caprolactone) and polyurethane scaffolds did not pose considerable cytotoxicity.Conclusion. Poly(ε-caprolactone) and polyurethane scaffolds did not exhibit cytotoxic effects and can be used for manufacturing polymer scaffolds of vascular grafts.

Experimental investigation of adhesion force, folding factor and surface roughness of chronic lymphocytic leukemia cell using AFM

In this paper, the Morphological properties, Contact Mechanics, Adhesion, Roughness and Folding of Chronic Lymphocytic Leukemia (CLL) cells have been examined utilizing Atomic Force Microscopy (AFM). The results show that the morphology of the CLL cell is spherical, with an average surface roughness of 23.06 nm and 5.34% folds. Adhesion force and work of adhesion of CLL cells is in the range of 23.2 ± 15.6% nN and 1484.6 ± 13.1% nJ, respectively. DMT and BCP contact theories have been more accurate than Hertz theory in characterizing the mechanical contact behavior of CLL cells due to the consideration of adhesion properties. Also, applying the folding factor in the Hertz, DMT and BCP contact theories, for the same contact force predicts a larger contact radius and a smaller indentation depth, and the accuracy of its results has increased compared to the smooth state.

Optimizing alkaline hydrothermal treatment for biomimetic smart metallic orthopedic and dental implants

Orthopedic and dental implant failure continues to be a significant concern due to localized bacterial infections. Previous studies have attempted to improve implant surfaces by modifying their texture and roughness or coating them with antibiotics to enhance antibacterial properties for implant longevity. However, these approaches have demonstrated limited effectiveness. In this study, we attempted to engineer the titanium (Ti) alloy surface biomimetically at the nanometer scale, inspired by the cicada wing nanostructure using alkaline hydrothermal treatment (AHT) to simultaneously confer antibacterial properties and support the adhesion and proliferation of mammalian cells. The two modified Ti surfaces were developed using a 4 h and 8 h AHT process in 1 N NaOH at 230 °C, followed by a 2-hour post-calcination at 600 °C. We found that the control plates showed a relatively smooth surface, while the treatment groups (4 h & 8 h AHT) displayed nanoflower structures containing randomly distributed nano-spikes. The results demonstrated a statistically significant decrease in the contact angle of the treatment groups, which increased wettability characteristics. The 8 h AHT group exhibited the highest wettability and significant increase in roughness 0.72 ± 0.08 µm (P < 0.05), leading to more osteoblast cell attachment, reduced cytotoxicity effects, and enhanced relative survivability. The alkaline phosphatase activity measured in all different groups indicated that the 8 h AHT group exhibited the highest activity, suggesting that the surface roughness and wettability of the treatment groups may have facilitated cell adhesion and attachment and subsequently increased secretion of extracellular matrix. Overall, the findings indicate that biomimetic nanotextured surfaces created by the AHT process have the potential to be translated as implant coatings to enhance bone regeneration and implant integration.Graphical

Phytoconstituent-derived zingerone nanoparticles disrupt the cell adhesion mechanism and suppress cell motility in melanoma B16F10 cells

Combining phytochemicals and nanotechnology to improve the unfavorable innate properties of phytochemicals and develop them into potent nanomedicines to enhance antitumor efficacy has become a novel strategy for cancer chemoprevention. Melanoma is the most aggressive, metastatic, and deadly disease of the primary cutaneous neoplasms. In this study, we fabricated phytoconstituent-derived zingerone nanoparticles (NPs) and validated their effects on cell adhesion and motility in melanoma B16F10 cells. Our data indicated that zingerone NPs significantly induced cytotoxicity and anti-colony formation and inhibited cell migration and invasion. Moreover, zingerone NPs dramatically interfered with the cytoskeletal reorganization and markedly delayed the period of cell adhesion. Our results also revealed that zingerone NPs-mediated downregulation of MMPs (matrix metalloproteinases) activity is associated with inhibiting cell adhesion and motility. We further evaluated the effects of zingerone NPs on Src/FAK /Paxillin signaling, our data showed that zingerone NPs significantly inhibited the protein activities of Src, FAK, and Paxillin, indicating that they play important roles in zingerone NP-mediated anti-motility and anti-invasion in melanoma cells. Accordingly, the phytoconstituent-zingerone NPs can strengthen the inhibition of tumor growth, invasion, and metastasis in malignant melanoma. Altogether, these multi-pharmacological benefits of zingerone NPs will effectively achieve the purpose of melanoma prevention and invasion inhibition.

Preparation and Immobilization Mechanism on a Novel Composite Carrier PDA-CF/PUF to Improve Cells Immobilization and Xylitol Production.

The preparation of a novel composite carrier of polydopamine-modified carbon fiber/polyurethane foam (PDA-CF/PUF) was proposed to improve cell immobilization and the fermentation of xylitol, which is an important food sweetener and multifunctional food additive. Candida tropicalis was immobilized on the composite carrier by adsorption and covalent binding. The properties and immobilization mechanism of the composite carrier and its effect on immobilized cells were investigated. It showed that the modification of PDA enhanced the loading of CF on the PUF surface and the adhesion of cells on the composite carrier surface. Also, the biocompatibility of carriers to cells was improved. In addition, the introduction of PDA increased the active groups on the surface of the carrier, enhanced the hydrophilicity, promoted the cells immobilization, and increased the xylitol yield. It was also found that expression of the related gene XYL1 in cells was significantly increased after the immobilization of the PDA-CF/PUF composite carrier during the fermentation. The PDA-CF/PUF was an immobilized carrier with the excellent biocompatibility and immobilization performance, which has great development potential in the industrial production of xylitol.

Nanofibrous electroconductive scaffolds composed of poly(vinyl alcohol) and modified polyaniline for skin tissue engineering application

AbstractNanofibrous electroconductive scaffolds were designed and fabricated using electrospinning approach based on a poly(vinyl alcohol)‐grafted polyaniline (PVA‐g‐PANI) and neat PVA with various PVA‐g‐PANI content for skin tissue engineering (STE) application. At first, phenylamine‐functionalized PVA macromonomer was synthesized, and then aniline was grafted onto macromonomer by an oxidation polymerization technique. The resultant PVA‐g‐PANI with different ratios was co‐electrospun with PVA to afford PVA‐g‐PANI/PVA electrically conductive nanofibrous scaffolds. Physicochemical features of the scaffolds, including water uptake properties, surface wettabilities, and morphologies as well as biological properties such as biodegradabilities, cytocompatibilities, cells adhesion and proliferation potentials, hemolysis rates, and protein adsorption capacities were investigated. Surface wettabilities of the scaffolds were altered from 55.7° for pure PVA up to 105.1° for the scaffold with the highest PVA‐g‐PANI content (30 wt%). It was found that the biodegradation rates of the scaffolds were decreased by increasing PVA‐g‐PANI content owing to very low biodegradation nature of PANI. Hemolysis assay revealed that all scaffolds were nonhemolytic (hemolysis rate &lt;2%), except the scaffold that fabricated with 30 wt% of PVA‐g‐PANI. As results, the constructed scaffolds with 15 and 20 wt% of PVA‐g‐PANI (S3 and S4, respectively) exhibited higher potentials in both physicochemical and biological properties for STE application.

Bio-refinery of palm kernel expeller waste into attached microalgal biodiesel, the life cycle analysis of waste biomass-to-energy

The exploitation of solid carbon waste in the form of palm kernel expeller served two purposes: (i) providing nutrients for microalgal growth and (ii) serving as a medium for the adhesion of microalgal cells. This study examined the life cycle assessment of biodiesel production from attached microalgae, a less explored domain as compared with conventional microalgal system focusing on energy and environmental feasibility aspect. The computed environmental impact indicated that harvesting and lipid production had contributed significantly to the overall impact, though the global warming potential remained low (5.2 × 10−4 kg CO2 eq.). The establishment of scenario analysis had revealed that solvent recovery options resulted in about 48–55 % damage recovery, giving significant decline in the environmental impacts. In terms of energy sustainability, the study revealed a net energy ratio of 0.52, suggesting that the energy output is less than the energy invested. While falling short of ideal energy sustainability, the ratio surpassed that of conventional petroleum diesel and many previous microalgal technologies. Despite challenges, the findings accentuated the importance of continuous improvement in microalgal biofuel processes for enhancing energy efficiency and reducing environmental impact.

Effect of Fibroblast Growth Factor 2 and Low-Level Laser Therapy on the Adhesion and Proliferation of Periodontal Ligament Stem Cells.

Introduction: The adhesion ability of mesenchymal stem cells can significantly affect their viability and is considered a prerequisite for cell therapy. The current study sought to evaluate the effect of fibroblast growth factor 2 (FGF2) and low-level laser therapy (LLLT), either individually or in conjunction, on the adhesion and proliferation of periodontal ligament stem cells (PDLSCs) when applied on the first day of cell seeding. Methods: The experimental groups of this study comprised a control group and different combinations of adjunctive FGF2 (50 ng/mL) and LLLT with an 808 nm diode laser in one (LLLT-1) or two sessions (LLLT-2) of irradiation. The proliferation and adhesion of cells were evaluated by using the methylthiazolyl tetrazolium (MTT) assay and 4',6-diamidino-2-phenylindole (DAPI) staining. All experiments were done in triplicates on the first, third, and fifth days after cell seeding. Two-way ANOVA and post hoc Tukey tests were used to analyze the data of the MTT assay. P<0.05 was considered statistically significant. Results: One-day post-culture, only significant differences were found between the control group and the FGF2 (P=0.04) and FGF2+LLLT-2 application (P=0.04) groups. After three days post-cell culture, only a significantly higher proliferation rate was found in the control group than in the FGF2 group (P=0.01). After five days, the control group and LLLT-2 groups showed significantly higher amounts of proliferation compared to the other groups (P<0.05). DAPI staining qualitatively confirmed the results of the MTT assay. Conclusion: The LLLT can be applied to PDLSCs on the day of seeding without causing a notable decrease in their viability and adhesion. Conversely, the administration of FGF2 should be restricted on the seeding day and postponed to subsequent days as it may have adverse effects on their adhesion and proliferation.

Zwitterionic sulfobetaine methacrylate (SBMA) coating on hydrophobic acrylic intraocular lens material to prevent the adhesion of lens epithelial cells: Effect of SBMA concentration

Posterior capsular opacification (PCO), known as a prevalent complication of cataract surgery, occurs because of the attachment and abnormal proliferation of remaining lens epithelial cells (LECs) after cataract surgery. To reduce the PCO occurrence by improving cell adhesion resistance, we attempted zwitterionic sulfobetaine methacrylate (SBMA) coating through ultraviolet-induced graft polymerization on the surfaces of intraocular lens (IOL) materials. In this study, the effect of the concentration of SBMA monomers in the coating solutions adjusted from 10 wt% to 30 wt% was investigated on the chemical composition, morphology, and hydrophilicity of the IOL material surfaces modified with SBMA. Additionally, the effect of SBMA concentration on preventing adhesion to protein and LECs on the surfaces of SBMA-modified IOL materials was evaluated in vitro. Grafting of zwitterionic SBMA on the surfaces of hydrophobic acrylic IOL materials was confirmed by Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy and water contact angle (WCA). To evaluate the long-term hydrophilicity of coating films prepared with different concentrations of SBMA on the IOL material surfaces, the WCA of IOL materials stored in phosphate-buffered saline solution was measured as a function of time. The coating film prepared at a concentration of 20 wt% of SBMA showed the lowest WCA after 28 days, showing the best long-term hydrophilicity. Also, that prepared at a concentration of 20 wt% of SBMA exhibited the highest anti-adhesion effect on proteins and LECs.

Tandem Mass Tag-based proteomic analysis of protein changes in superchilled crayfish (Procambarus clarkii) presoaked with carrageenan oligosaccharides

To assess the effectiveness of carrageenan oligosaccharides (COs) in enhancing superchilling storage of crayfish, the physicochemical features of muscle and protein abundance in the refrigerated sample (RS), superchilled sample (SS) and COs soaked superchilled sample (CS) were evaluated. Microstructural and SDS-PAGE analyses suggested that CS exhibited fewer pores, with a microstructure and protein subunits distribution more similar to RS. Tandem Mass Tags quantitative proteomic analysis revealed 66 up-regulated differentially abundant proteins (DAPs) in the CS vs. SS batch, including myosin light chain 2, neural cadherin, integrin beta, lectin-like protein, toll-1, reticulon-1, and moesin/ezrin/radixin homolog 1, which facilitate cells adhesion and maintain membrane/cytoskeleton integrity. Eukaryotic Clusters of Orthologous Groups results confirmed that COs treatment increased the stability of crayfish myofibrillar proteins by up-regulating DAPs, which were concentrated in functional categories such as “posttranslation modification, protein turnover, chaperones”, “signal transduction mechanisms”, “energy production and conversion”, and “cytoskeleton”.

The Osteogenic Peptide P-15 for Bone Regeneration: A Narrative Review of the Evidence for a Mechanism of Action.

Bone regeneration is a complex multicellular process involving the recruitment and attachment of osteoprogenitors and their subsequent differentiation into osteoblasts that deposit extracellular matrixes. There is a growing demand for synthetic bone graft materials that can be used to augment these processes to enhance the healing of bone defects resulting from trauma, disease or surgery. P-15 is a small synthetic peptide that is identical in sequence to the cell-binding domain of type I collagen and has been extensively demonstrated in vitro and in vivo to enhance the adhesion, differentiation and proliferation of stem cells involved in bone formation. These events can be categorized into three phases: attachment, activation and amplification. This narrative review summarizes the large body of preclinical research on P-15 in terms of these phases to describe the mechanism of action by which P-15 improves bone formation. Knowledge of this mechanism of action will help to inform the use of P-15 in clinical practice as well as the development of methods of delivering P-15 that optimize clinical outcomes.

Retracted] 2,3,5,4‑tetrahydroxy diphenylethylene‑2‑O‑glucoside inhibits the adhesion and invasion of A549 human lung cancer cells.

Following the publication of this paper, it was drawn to the Editor's attention by a concerned reader that the data featured in Figs. 1, 4 and 5 (including western blotting data) were strikingly similar to data that had appeared in a different form in a different article by different authors at different research institutes. Owing to the fact that the contentious data in the above article had already been accepted for publication in another article prior to its submission to Molecular Medicine Reports, the Editor has decided that this paper should be retracted from the Journal. The authors were asked for an explanation to account for these concerns, but the Editorial Office did not receive a reply. The Editor apologizes to the readership for any inconvenience caused. [Molecular Medicine Reports 16: 8900‑8906, 2017; DOI: 10.3892/mmr.2017.7680].

Development of novel hybrid nanomaterials with potential application in bone/dental tissue engineering: design, fabrication and characterization enriched-SAPO-34/CS/PANI scaffold

ABSTRACT Fe-Ca-SAPO-34/CS/PANI, a novel hybrid bio-composite scaffold with potential application in dental tissue engineering, was prepared by freeze drying technique. The scaffold was characterized using FT-IR and SEM methods. The effects of PANI on the physicochemical properties of the Fe-Ca-SAPO-34/CS scaffold were investigated, including changes in swelling ratio, mechanical behavior, density, porosity, biodegradation, and biomineralization. Compared to the Fe-Ca-SAPO-34/CS scaffold, adding PANI decreased the pore size, porosity, swelling ratio, and biodegradation, while increasing the mechanical strength and biomineralization. Cell viability, cytotoxicity, and adhesion of human dental pulp stem cells (hDPSCs) on the scaffolds were investigated by MTT assay and SEM. The Fe-Ca-SAPO-34/CS/PANI scaffold promoted hDPSC proliferation and osteogenic differentiation compared to the Fe-Ca-SAPO-34/CS scaffold. Alizarin red staining, alkaline phosphatase activity, and qRT-PCR results revealed that Fe-Ca-SAPO-34/CS/PANI triggered osteoblast/odontoblast differentiation in hDPSCs through the up-regulation of osteogenic marker genes BGLAP, RUNX2, and SPARC. The significance of this study lies in developing a novel scaffold that synergistically combines the beneficial properties of Fe-Ca-SAPO-34, chitosan, and PANI to create an optimized microenvironment for dental tissue regeneration. These findings highlight the potential of the Fe-Ca-SAPO-34/CS/PANI scaffold as a promising biomaterial for dental tissue engineering applications, paving the way for future research and clinical translation in regenerative dentistry.

Platelet-rich fibrin (PRF) modified nano-hydroxyapatite/chitosan/gelatin/alginate scaffolds increase adhesion and viability of human dental pulp stem cells (DPSC) and osteoblasts derived from DPSC

Bone tissue regeneration strategies have incorporated the use of natural polymers, such as hydroxyapatite (nHA), chitosan (CH), gelatin (GEL), or alginate (ALG). Additionally, platelet concentrates, such as platelet-rich fibrin (PRF) have been suggested to improve scaffold biocompatibility. This study aimed to develop scaffolds composed of nHA, GEL, and CH, with or without ALG and lyophilized PRF, to evaluate the scaffold's properties, growth factor release, and dental pulp stem cells (DPSC), and osteoblast (OB) derived from DPSC viability. Four scaffold variations were synthesized and lyophilized. Then, degradation, swelling profiles, and morphological analysis were performed. Furthermore, PDGF-BB and FGF-B growth factors release were quantified by ELISA, and cytotoxicity and cell viability were evaluated. The swelling and degradation profiles were similar in all scaffolds, with pore sizes ranging between 100 and 250 μm. FGF-B and PDGF-BB release was evidenced after 24 h of scaffold immersion in cell culture medium. DPSC and OB-DPSC viability was notably increased in PRF-supplemented scaffolds. The nHA-CH-GEL-PRF scaffold demonstrated optimal physical-biological characteristics for stimulating DPSC and OB-DPSC cell viability. These results suggest lyophilized PRF improves scaffold biocompatibility for bone tissue regeneration purposes.