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Characterization of quercetin and its glycoside derivatives in Malus germplasm
Lei Zhang,Qipeng Xu,Yaohua You,Weifeng Chen,Zhengcao Xiao,Pengmin Li,Fengwang Ma 한국원예학회 2018 Horticulture, Environment, and Biotechnology Vol.59 No.6
Quercetin and its glycoside derivatives were identifi ed and quantifi ed using high-performance liquid chromatograph (HPLC)and liquid chromatograph/mass spectrometer/mass spectrometer (LC/MS/MS) in the leaves, flowers, and fruits of 22 Malusgenotypes. In all genotypes, small amounts of quercetin aglycone were present, with water-soluble glycoside forms were themost abundant in diff erent Malus plant tissues, including quercetin-3-galactoside, quercetin-3-rutinoside, quercetin-3-glucoside,quercetin-3-xyloside, quercetin-3-arabinoside, and quercetin-3-rhamnoside. Among these six quercetin glycosides,quercetin-3-galactoside was the common form in Malus plants, except in the leaves and flowers of M. ceracifolia and M. magdeburgensis , and in the fruits of M. micromalus ‘Haihong Fruit’, where there was a higher concentration of quercetin-3-glucoside. Among the diff erent tissues tested, leaves contained the highest concentration of quercetin and its glycosides,while fruits contained the lowest concentrations of these compounds. Among the genotypes we analyzed, no specifi c genotypeconsistently contained the highest concentration of quercetin and its glycoside derivatives. M. domestica ‘Honeycrisp’had the highest total compound concentration (approximately 1600 mg kg −1 ), whereas M. hupehensis contained the lowestin its fruits. In contrast, the concentration of total quercetin and its glycosides was more than 5000 mg kg −1 in the leaves ofeight genotypes and greater than 2500 mg kg −1 in the flowers of seven species. In general, the concentration of quercetinand its glycoside derivatives depended on the species and tissue type. These results may provide useful information for theevaluation and selection of edible Malus fruits and the materials for quercetin glycoside extraction.
Ying Yang,Dong Wang,Lei Cui,Hong-Hao Ma,Li Zhang,Hong-Yun Lian,Qing Zhang,Xiao-Xi Zhao,Li-Ping Zhang,Yun-Ze Zhao,Na Li,Tian-You Wang,Zhi-Gang Li,Rui Zhang 대한암학회 2021 Cancer Research and Treatment Vol.53 No.1
Purpose We sought to investigate the effectiveness and safety of dabrafenib in children with BRAFV600E-mutated Langerhans cell histiocytosis (LCH). Materials and Methods A retrospective analysis was performed on 20 children with BRAFV600E-mutated LCH who were treated with dabrafenib. Results The median age at which the patients started taking dabrafenib was 2.3 years old (range, 0.6 to 6.5 years). The ratio of boys to girls was 2.3:1. The median follow-up time was 30.8 months (range, 18.9 to 43.6 months). There were 14 patients (70%) in the risk organ (RO)+ group and six patients (30%) in the RO– group. All patients were initially treated with traditional chemotherapy and then shifted to targeted therapy due to poor control of LCH or intolerance to chemotherapy. The overall objective response rate and the overall disease control rate were 65% and 75%, respectively. During treatment, circulating levels of cell-free BRAFV600E (cfBRAFV600E) became negative in 60% of the patients within a median period of 3.0 months (range, 1.0 to 9.0 months). Grade 2 or 3 adverse effects occurred in five patients. Conclusion Some children with BRAFV600E-mutated LCH may benefit from monotherapy with dabrafenib, especially high-risk patients with concomitant hemophagocytic lymphohistiocytosis and intolerance to chemotherapy. The safety of dabrafenib is notable. A prospective study with a larger sample size is required to determine the optimal dosage and treatment duration.
Rana Naveed Ur Rehman,Yaohua You,Sajid Ali,Yule Wang,Lei Zhang,Pengmin Li,Fengwang Ma 한국원예학회 2018 Horticulture, Environment, and Biotechnology Vol.59 No.1
Polyphenol intermediates accumulate predominantly in peripheral parts of floral tissues and play various roles in tissuehomeostasis. A limited ornamental flower shelf life is caused by early tissue senescence, otherwise known as programmedcell death (PCD), which is characterized by processes such as DNA degradation, reduction in protein content and others. However, the role of polyphenols during PCD is poorly understood. In this study, we evaluated polyphenols as potentialbiochemical markers during developmental changes associated with PCD. Malus crabapple flowers were exposed to low(LT = 13 ± 2 °C), room (RT = 23 ± 2 °C), and high (HT = 30 ± 2 °C) temperatures to induce different levels of PCD. HTtreatment was associated with enhanced H2O2and MDA content, which subsequently caused lower protein concentrationand induced DNA degradation. Conversely, substantially higher protein content, lesser DNA degradation, and lower H2O2and MDA accumulation were observed following RT and LT treatments. Furthermore, significantly higher concentrationsof phenolic acids, flavanols, and anthocyanins were observed following both RT and LT treatments, more so for the latter,due to up-regulation of structural genes such as MpPAL, MpDFR, MpLDOX, and MpUFGT. Similarly, following HT treatmentthat induced a higher rate of PCD, the accumulation of dihydrochalcone and flavonols was significantly enhanced andassociated with increased expression of MpCHS and MpFLS. Phenolic contents are determined via precise regulation of ahighly conserved set of structural genes, indicating their functional importance. Therefore, it was assumed that individualphenolic intermediates or discrete diverse classes of polyphenol compounds may be utilized as biochemical markers of PCDin woody ornamental flowers of Malus crabapple.
Kan Hao,Zhang Ka,Mao Aiqin,Geng Li,Gao Mengru,Feng Lei,You Qingjun,Ma Xin 생화학분자생물학회 2021 Experimental and molecular medicine Vol.53 No.-
The aorta contains numerous cell types that contribute to vascular inflammation and thus the progression of aortic diseases. However, the heterogeneity and cellular composition of the ascending aorta in the setting of a high-fat diet (HFD) have not been fully assessed. We performed single-cell RNA sequencing on ascending aortas from mice fed a normal diet and mice fed a HFD. Unsupervised cluster analysis of the transcriptional profiles from 24,001 aortic cells identified 27 clusters representing 10 cell types: endothelial cells (ECs), fibroblasts, vascular smooth muscle cells (SMCs), immune cells (B cells, T cells, macrophages, and dendritic cells), mesothelial cells, pericytes, and neural cells. After HFD intake, subpopulations of endothelial cells with lipid transport and angiogenesis capacity and extensive expression of contractile genes were defined. In the HFD group, three major SMC subpopulations showed increased expression of extracellular matrix-degradation genes, and a synthetic SMC subcluster was proportionally increased. This increase was accompanied by upregulation of proinflammatory genes. Under HFD conditions, aortic-resident macrophage numbers were increased, and blood-derived macrophages showed the strongest expression of proinflammatory cytokines. Our study elucidates the nature and range of the cellular composition of the ascending aorta and increases understanding of the development and progression of aortic inflammatory disease.