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.

     

不同苹果砧穗组合的生长及光合特性

以‘垂丝海棠’（Malus halliana）和‘平邑甜茶’（Malus hupehensis）为基砧,分别嫁接品种‘烟富6号’和‘长富2号’接穗,测定4种砧穗组合的嫁接亲和性、接穗生长量、光合与荧光参数及叶绿素含量（SPAD）,并用主成分分析法综合评价砧穗组合的优劣,探讨不同苹果砧穗组合嫁接苗的生长及光合特性,为西北盐碱地选择适宜的苹果砧木提供理论依据。结果表明：（1）4种砧穗组合中‘垂丝海棠/烟富6号’的上下口粗度比最接近1,嫁接亲和性最好。（2）整个生长期内,以‘垂丝海棠’为基砧的2个组合嫁接苗的生长量、净光合速率（P_n）、最大荧光（F_m）、PSⅡ最大光能转化率（F_v/F_m）均显著大于‘平邑甜茶’为基砧的组合,但其胞间CO₂浓度（C_i）及初始荧光（F₀）显著低于‘平邑甜茶’为基砧的组合;光化学猝灭系数（qP）在4种砧穗组合中无显著差异。（3）在8月份光照强度较高时,‘垂丝海棠/烟富6号’ 嫁接苗的气孔导度（G_s）高于其他砧穗组合;以‘垂丝海棠’为基砧的2个组合嫁接苗叶片的蒸腾速率（T_r）和相对叶绿素含量（SPAD）显著高于‘平邑甜茶’ 基砧组合。（4）根据主成分分析对各项指标进行综合评价,按照4个砧穗组合的综合得分由高到低依次为：‘垂丝海棠/烟富6号’、‘垂丝海棠/长富2号’、‘平邑甜茶/长富2号’、‘平邑甜茶/烟富6号’。研究发现,基砧‘垂丝海棠’的适应性优于‘平邑甜茶’,且‘垂丝海棠/烟富6号’砧穗组合的嫁接亲和性高,长势强,光合能力优,为甘肃中部地区适宜的砧穗组合。     

Revealing the Inhibitory Effect of Ginseng on Mitochondrial Respiration through Synaptosomal Proteomics

Ginseng, the active ingredients of which are ginsenosides, is the most popular herbal medicine and has potential merit in the treatment of cerebral disorders. To better understand the function of Ginseng in the cerebral system, we examined changes in the protein expression profiles of synaptosomes extracted from the cerebral cortical and hippocampal tissues of rats administered a high or low dose of Ginseng for 2 weeks. More than 5000 proteins belonging to synaptosomes were simultaneously identified and quantitated by an approach combining tandem mass tags with 2D liquid chromatography‐mass spectrometry (LC‐MS). Regarding differentially expressed proteins, downregulated proteins were much more highly induced than upregulators in the cerebral cortical and hippocampal synaptosomes, regardless of the dose of Ginseng. Bioinformatic analysis indicated the majority of the altered proteins to be located in the mitochondria, directly or indirectly affecting mitochondrial oxidative respiration. Further functional experiments using the substrate‐uncoupler inhibitor titration approach confirmed that three representative ginsenosides were able to inhibit oxidative phosphorylation in mitochondria. Our results demonstrate that Ginseng can regulate the function of mitochondria and alter the energy metabolism of cells, which may be useful for the treatment of central nervous disorders.     

Structure-based design and structure-activity relationships of 1,2,3,4-tetrahydroisoquinoline derivatives as potential PDE4 inhibitors

This paper describes our medicinal chemistry efforts on 7-(cyclopentyloxy)-6-methoxy1,2,3,4-tetrahydroisoquinoline scaffold: design, synthesis and biological evaluation using conformational restriction approach and bioisosteric replacement strategy. Biological data revealed that the majority of the synthesized compounds of this series displayed moderate to potent inhibitory activity against PDE4B and strong inhibition of LPS-induced TNFα release. Among them, compound 19 exhibited the strongest inhibition against PDE4B with an IC₅₀ of 0.88?µM and 21 times more potent selectivity toward PDE4B over PDE4D when compared to rolipram. A primary structure-activity relationship study showed that the attachment of CH₃O group or CF₃O group to the phenyl ring at the para-position was helpful to enhance the inhibitory activity against PDE4B. Moreover, sulfonamide group played a key role in improving the inhibitory activity against PDE4B and subtype selectivity. In addition, the attachment of the additional rigid substituents at the C-3 position of 1,2,3,4-tetrahydroisoquinoline ring was favored to subtype selectivity, which was consistent well with the observed docking simulation.