Effect of substrate stiffness on proliferation and differentiation of periodontal ligament stem cells

Objectives

The aim of this study was to understand the effect of substrate stiffness (a mechanical factor of the extracellular matrix) on periodontal ligament stem cells (PDLSCs) and its underlying mechanism.

Materials and methods

Elastic substrates were fabricated by mixing 2 components, a base and curing agent in proportions of 10:1, 20:1, 30:1 or 40:1. PDLSC morphology was observed using scanning electron microscopy (SEM). Cell proliferation and differentiation were assessed after PDLSCs was cultured on various elastic substrates. Data were analysed using one‐way ANOVA.

Results

SEM revealed variations in the morphology of PDLSCs cultured on elastic substrates. PDLSC proliferation increased with substrate stiffness (P < .05). Osteogenic differentiation of PDLSCs was higher on stiff substrates. Notch pathway markers were up‐regulated in PDLSCs cultured on stiff substrates.

Conclusions

Results suggested that the osteogenic differentiation of PDLSCs might be promoted by culturing them in a stiffness‐dependent manner, which regulates the Notch pathway. This might provide a new method of enhancing osteogenesis in PDLSCs.

     

Aptamer‐mediated synthesis of multifunctional nano‐hydroxyapatite for active tumour bioimaging and treatment

ObjectivesThe nano‐hydroxyapatite (nHAp) is widely used to develop imaging probes and drug carriers due to its excellent bioactivity and biocompatibility. However, traditional methods usually need cumbersome and stringent conditions such as high temperature and post‐modification to prepare the functionalized nHAp, which do not benefit the particles to enter cells due to the increased particle size. Herein, a biomimetic synthesis strategy was explored to achieve the AS1411‐targeted tumour dual‐model bioimaging using DNA aptamer AS1411 as a template. Then, the imaging properties and the biocompatibility of the synthesized AS‐nFAp:Gd/Tb were further investigated.Materials and methodsThe AS‐nFAp:Gd/Tb was prepared under mild conditions through a one‐pot procedure with AS1411 as a template. Besides, the anticancer drug DOX was loaded to AS‐nFAp:Gd/Tb so as to achieve the establishment of a multifunctional nano‐probe that integrated the tumour diagnosis and treatment. The AS‐nFAp:Gd/Tb was characterized by transmission electron microscopy (TEM), energy disperse X‐ray Spectroscopy (EDS) mapping, X‐ray photoelectron spectroscopy (XPS) spectrum, X‐ray diffraction (XRD), fourier‐transformed infrared (FTIR) spectroscopy, capillary electrophoresis analyses, zeta potential and particle sizes. The in vitro magnetic resonance imaging (MRI) and fluorescence imaging were performed on an MRI system and a confocal laser scanning microscope, respectively. The potential of the prepared multifunctional nHAp for a targeted tumour therapy was investigated by a CCK‐8 kit. And the animal experiments were conducted on the basis of the guidelines approved by the Animal Care and Use Committee of Sichuan University, China.ResultsIn the presence of AS1411, the as‐prepared AS‐nFAp:Gd/Tb presented a needle‐like morphology with good monodispersity and improved imaging performance. Furthermore, due to the specific binding between AS1411 and nucleolin up‐expressed in cancer cells, the AS‐nFAp:Gd/Tb possessed excellent AS1411‐targeted fluorescence and MRI imaging properties. Moreover, after loading chemotherapy drug DOX, in vitro and in vivo studies showed that DOX@AS‐nFAp:Gd/Tb could effectively deliver DOX to tumour tissues and exert a highly effective tumour inhibition without systemic toxicity compared with pure DOX.ConclusionsThe results indicated that the prepared multifunctional nHAp synthesized by a novel biomimetic strategy had outstanding capabilities of recognition and treatment for the tumour and had good biocompatibility; hence, it might have a potential clinical application in the future.     

Tunable Terahertz Plasmonic Perfect Absorber Based on T-Shaped InSb Array

High absorption efficiency is particularly desirable for various microtechnological applications. In this paper, a nearly perfect terahertz absorber for transverse magnetic (TM) polarization based on T-shaped InSb array is proposed and numerically investigated. Incident wave at the Fabry-Perot resonant frequency can be totally absorbed into the narrow grooves between the two adjacent T-shaped InSb arms. The absorption mechanism is theoretically and numerically studied by using the Fabry-Perot model and the finite element method (FEM), respectively. It is found that the proposed absorber has large angle tolerance. Moreover, the absorption peak can be controlled by varying the temperature. Furthermore, a new absorption peak will emerge while breaking the symmetry of the T-shaped InSb array. This tunable and angle-independent THz perfect absorber may find important applications in THz devices such as microbolometers, coherent thermal emitters, solar cells, photo detectors, and sensors.     

雅鲁藏布江流域NDVI变化与风沙化土地演变的耦合关系

运用1982-2010年的两种NDVI数据集（Pathfinder AVHRR和SPOT VEGETATION）,以及1975、1990、2000和2008年4期遥感数据,通过GIS技术、人工目视解译和灰色关联分析方法,研究了雅鲁藏布江流域NDVI变化和风沙化土地演变的耦合关系,结合1957-2007年降水和气温逐日气象资料,探讨了气候变化对其耦合关系的影响。结果表明：（1）流域内1982-2010年NDVI的年际变化总体上呈波动式增长的趋势。NDVI空间分布呈现由下游向中上游逐渐降低的趋势,以米林宽谷最大、马泉河宽谷最小。（2）2008年流域内共有风沙化土地273 697.54hm²,呈现由江源区马泉河宽谷向中下游递减的趋势。1975-2008年流域内风沙化土地呈缓慢增长趋势,以1990-1999年增长率最高,2000-2008年的增长率最小。（3）对于NDVI年变化和植被生长季（7-9月份）的变化,马泉河宽谷受平均气温的影响最大,日喀则宽谷和山南宽谷受年降水量的影响最大;米林宽谷NDVI的年变化受风沙化土地扩展的影响最大,植被生长季变化受年降水量的影响最大。（4）不同宽谷段NDVI与风沙化土地年变化的关联度自下游向中上游呈总体减小的趋势。流域尺度NDVI植被生长季变化主要受平均气温和年降水量的影响,非植被生长季（10月-翌年6月）变化主要受风沙化土地扩展的影响。     

Doxorubicin conjugated carbon dots as a drug delivery system for human breast cancer therapy

Objectives

Carbon dots (CDs) are one of the most promising carbon‐based materials in bioimaging and drug/gene delivery applications. In this study, we have attempted to study the drug carrying capacity of highly fluorescent CDs for delivery of doxorubicin (DOX) and investigate the therapeutic activity of the CDs‐DOX drug delivery system.

Materials and methods

Carbon dots were synthesized by means of a hydrothermal approach with mixing citric acid and ethylenediamine. The properties of CDs were characterized in respects of spectral property, zeta potential, particle morphology and chemical composition. The drug loading efficiency (DLE) and release profile of CDs‐DOX were determined by a fluorescence spectrophotometer. We investigated the cellular toxicity and pharmaceutical activity of CDs and CDs‐DOX in L929 cells and MCF‐7 cells by the CCK‐8 assay. We also studied the cellular uptake of CDs‐DOX with the methods of confocal microscopy and flow cytometry. In addition, the effect of CDs‐DOX on cell apoptosis was assessed by flow cytometry.

Results

The obtained CDs possessed good biocompatibility and showed a potential capacity of promoting proliferation. DOX was successfully conjugated to CDs through electrostatic interaction, and the results of the DLE and loading content (DLC) suggested a relatively high drug loading capacity of CDs. Compared with free DOX, the CDs‐DOX complex had a higher cellular uptake and better anti‐tumour efficacy on MCF‐7 cells.

Conclusions

The results of this study indicated that the CDs‐DOX drug delivery system had a potential value in cancer chemotherapeutic application.