Ginkgo biloba Extract Individually Inhibits JNK Activation and Induces c-Jun Degradation in Human Chondrocytes: Potential Therapeutics for Osteoarthritis

Osteoarthritis (OA) is a common joint disorder with varying degrees of inflammation. The ideal anti-OA drug should have immunomodulatory effects while at the same time having limited or no toxicity. We examined the anti-inflammatory effects of Ginkgo biloba extract (EGb) in interleukin-1 (IL-1)-stimulated human chondrocytes. Chondrocytes were prepared from cartilage specimens taken from patients with osteoarthritis who had received total hip or total knee replacement. The concentrations of chemokines and the degree of cell migration were determined by ELISA and chemotaxis assays, respectively. The activation of inducible nitric oxide synthase (iNOS), mitogen-activated protein kinases (MAPKs), activator protein-1 (AP-1), and nuclear factor-kappaB (NF-κB) was determined by immunoblotting, immunohistochemistry, and electrophoretic mobility shift assay. We found that EGb inhibited IL-1-induced production of chemokines, which in turn resulted in attenuation of THP-1 cell migration toward EGb-treated cell culture medium. EGb also suppressed IL-1-stimulated iNOS expression and release of nitric oxide (NO). The EGb-mediated suppression of the iNOS-NO pathway correlated with the attenuation of activator protein-1 (AP-1) but not nuclear factor-kappaB (NF-κB) DNA-binding activity. Of the mitogen-activated protein kinases (MAPKs), EGb inhibited only c-Jun N-terminal kinase (JNK). Unexpectedly, EGb selectively caused degradation of c-Jun protein. Further investigation revealed that EGb-mediated c-Jun degradation was preceded by ubiquitination of c-Jun and could be prevented by the proteosome inhibitor MG-132. The results imply that EGb protects against chondrocyte degeneration by inhibiting JNK activation and inducing ubiquitination-dependent c-Jun degradation. Although additional research is needed, our results suggest that EGb is a potential therapeutic agent for the treatment of OA.     

Chondroprotective effects and mechanisms of resveratrol in advanced glycation end products-stimulated chondrocytes

Introduction  

Accumulation of advanced glycation end products (AGEs) in joints contributes to the pathogenesis of cartilage damage in osteoarthritis (OA). We aim to explore the potential chondroprotective effects of resveratrol on AGEs-stimulated porcine chondrocytes and cartilage explants.     

The Walker B motif of the second nucleotide-binding domain (NBD2) of CFTR plays a key role in ATPase activity by the NBD1-NBD2 heterodimer

CFTR (cystic fibrosis transmembrane conductance regulator), a member of the ABC (ATP-binding cassette) superfamily of membrane proteins, possesses two NBDs (nucleotide-binding domains) in addition to two MSDs (membrane spanning domains) and the regulatory 'R' domain. The two NBDs of CFTR have been modelled as a heterodimer, stabilized by ATP binding at two sites in the NBD interface. It has been suggested that ATP hydrolysis occurs at only one of these sites as the putative catalytic base is only conserved in NBD2 of CFTR (Glu1371), but not in NBD1 where the corresponding residue is a serine, Ser573. Previously, we showed that fragments of CFTR corresponding to NBD1 and NBD2 can be purified and co-reconstituted to form a heterodimer capable of ATPase activity. In the present study, we show that the two NBD fragments form a complex in vivo, supporting the utility of this model system to evaluate the role of Glu1371 in ATP binding and hydrolysis. The present studies revealed that a mutant NBD2 (E1371Q) retains wild-type nucleotide binding affinity of NBD2. On the other hand, this substitution abolished the ATPase activity formed by the co-purified complex. Interestingly, introduction of a glutamate residue in place of the non-conserved Ser573 in NBD1 did not confer additional ATPase activity by the heterodimer, implicating a vital role for multiple residues in formation of the catalytic site. These findings provide the first biochemical evidence suggesting that the Walker B residue: Glu1371, plays a primary role in the ATPase activity conferred by the NBD1-NBD2 heterodimer.     

辽东山地古石河冰缘地貌森林生态系统苔藓物种多样性研究

基于9个20 m×30 m森林群落样地的调查数据,采用物种丰富度、α和β多样性指数,对辽东山地古石河冰缘地貌不同林型石生、树生苔藓植物物种多样性进行定量研究,采用皮尔逊相关分析方法对其影响因素进行分析。结果显示,古石河冰缘地貌苔藓植物共有26科46属59种;不同林型石生、树生苔藓植物物种丰富度和α多样性指数均为:暗针叶林针阔混交林落叶阔叶林;石生苔藓植物β多样性指数最高为落叶阔叶林-针阔混交林间(0.44),最低为落叶阔叶林-暗针叶林间(0.33);树生苔藓植物β多样性指数最高为针阔混交林-暗针叶林间(0.40),最低为落叶阔叶林-暗针叶林间(0.25);分析表明,林冠层郁闭度、海拔高度是影响辽东山地古石河冰缘地貌森林生态系统苔藓物种多样性的重要因子。     

基于EPG的三种刺吸式害虫在苹果苗上的取食行为比较

【目的】苹果绵蚜Eriosoma lanigerum、绣线菊蚜Aphis citricola和梨网蝽Stephanitis nashi是苹果园的一类重要害虫,它们以刺吸式口器对苹果树造成不同程度的危害。本研究旨在明确这3种刺吸式昆虫在苹果树上取食行为差异。【方法】利用刺吸电位(electrical penetration graph, EPG)技术对苹果绵蚜和绣线菊蚜成虫在苹果苗韧皮部和非韧皮部上的EPG指标,以及苹果绵蚜、绣线菊蚜和梨网蝽成虫苹果苗上的取食行为进行了比较分析,分析了这3种害虫的成虫在苹果苗上取食8 h各种波形平均持续时间的占比。【结果】结果表明,苹果绵蚜和绣线菊蚜成蚜在苹果苗上均产生6种取食波形,即非刺探波(np)、路径波(C)、意外穿刺细胞非主动取食细胞波(pd)、木质部取食波(G)、韧皮部唾液分泌波(E1)和韧皮部取食波(E2);而梨网蝽成虫取食过程中只产生非刺探波(np)、表皮刺穿波(A)、叶肉细胞取食波(Gc)和木质部取食波(E)4种波形。从蚜虫在苹果苗非韧皮部上取食的EPG指标看,苹果绵蚜成蚜pd波平均时间显著高于绣线菊蚜的,而刺探次数、np波总时间和pd波次数均显著低于绣线菊蚜的。从蚜虫在苹果苗韧皮部上取食的EPG指标来看,除第1次出现E2波的时间外,各指标没有显著差异。从3种害虫在苹果苗上取食8 h各波形的占比来看,梨网蝽成虫的np波总时间所占比例最高(53%),其次是绣线菊蚜成虫的(24%),苹果绵蚜成虫的最低(为1%)。同时,苹果绵蚜和绣线菊蚜成虫取食波为E2波,所占总时间比例分别为35%和25%,而梨网蝽的取食波为Gc波(占总时间比例为36%)和E波(占总时间比例为11%)。【结论】本研究阐释了苹果园刺吸式口器害虫的生态位分离和取食行为学机制,为果园刺吸式口器害虫的综合治理提供了理论依据。