Dihydromyricetin sensitizes human acute myeloid leukemia cells to retinoic acid-induced myeloid differentiation by activating STAT1

The success of all-trans retinoic acid (ATRA) in differentiation therapy for patients with acute promyelocytic leukemia (APL) highly encourages researches to apply a new combination therapy based on ATRA. Therefore, research strategies to further sensitize cells to retinoids are urgently needed. In this study, we showed that Dihydromyricetin (DMY), a 2,3-dihydroflavonol compound, exhibited a strong synergy with ATRA to promote APL NB4 cell differentiation. We observed that DMY sensitized the NB4 cells to ATRA-induced cell growth inhibition, CD11b expression, NBT reduction and myeloid regulator expression. PML-RARα might not be essential for DMY-enhanced differentiation when combined with ATRA, while the enhanced differentiation was dependent on the activation of p38-STAT1 signaling pathway. Taken together, our study is the first to evaluate the synergy of DMY and ATRA in NB4 cell differentiation and to assess new opportunities for the combination of DMY and ATRA as a promising approach for future differentiation therapy.     

Structural Basis of Protein Kinase Cα Regulation by the C-Terminal Tail

Protein kinase C (PKC) isoenzymes are multi-modular proteins activated at the membrane surface to regulate signal transduction processes. When activated by second messengers, PKC undergoes a drastic conformational and spatial transition from the inactive cytosolic state to the activated membrane-bound state. The complete structure of either state of PKC remains elusive. We demonstrate, using NMR spectroscopy, that the isolated Ca²⁺-sensing membrane-binding C2 domain of the conventional PKCα interacts with a conserved hydrophobic motif of the kinase C-terminal region, and we report a structural model of the complex. Our data suggest that the C-terminal region plays a dual role in regulating the PKC activity: activating, through sensitization of PKC to intracellular Ca²⁺ oscillations; and auto-inhibitory, through its interaction with a conserved positively charged region of the C2 domain.     

交联酶聚集体制备中钙离子的结构调控作用

以葡萄糖氧化酶(GOx)为研究对象,系统地研究了钙离子对交联酶聚集体(CLEA)粒子尺寸和微观结构的调控作用以及酶催化性能和实用性的影响。研究结果表明,GOx酶沉淀过程中引入钙离子可显著降低CLEA粒子尺寸并导致粒子内纳米孔道结构逐步消失。在0.1 mmol/L钙离子浓度下,GOx酶的CLEA仍保有清晰的纳米孔道结构。以葡萄糖为底物的GOx酶CLEA催化结果显示,该CLEA粒子的酶活性为对照CLEA粒子的2.69倍。即便1.0 mmol/L钙离子浓度下制备的CLEA粒子的GOx酶活性仍高出对照CLEA粒子约42%。此外,0.1 mmol/L钙离子浓度下制备的CLEA不仅具有更高的底物转化速率和很好的操作稳定性,而且CLEA中GOx酶的最大反应速度显著提高。这些实验结果明确了钙离子对CLEA粒子尺寸和微观结构的调控作用,为制备具有高效生物催化活性的CLEA粒子奠定了基础。     

城市化对合肥蝶类多样性的影响

2010年3—10月,沿城市发展梯度选取了合肥市3个区域(城市、城郊和农村),进行蝴蝶调查。共采集蝴蝶1484只,隶属7科28属34种。结果表明:研究区域优势种蝶类为菜粉蝶(Pieris rapae)、酢浆灰蝶(Pseudozizeeria maha)、黄钩蛱蝶(Polygonia c-aureum);合肥不同城市化区域蝶类多样性存在差异,其多样性指数变化趋势为农村城郊城市;农村和城郊的多样性指数和丰富度指数在7月最高,城市8月最高;城市和城郊的优势度指数在8月最高,农村7月最高;3种不同城市化区域的均匀度指数均是8月最高。在快速城市化过程中,应根据不同城市化水平、不同生境类型采取不同的措施,保护和促进城市生物多样性。     

长白山白桦林不同演替阶段土壤有机碳组分的变化

为了解长白山天然针阔混交林群落恢复演替土壤碳储量的变化,采用空间代替时间的方法,选取白桦幼龄林、白桦中龄林、白桦成熟林、阔叶红松成熟林和阔叶红松过熟林5个不同演替序列,研究其土壤总有机碳(SOC)、易氧化有机碳(ROC)、微生物生物量碳(MBC)及颗粒有机碳(POC)含量。结果表明:随着白桦林从早期到晚期的演替,SOC、MBC、ROC、POC以及土壤全氮、全磷和碳氮比(C/N)均呈现先逐渐增加后保持稳定的规律。随着土层深度的增加,SOC、MBC、ROC和POC含量均显著降低(P0.05),5个演替序列内ROC/SOC和POC/SOC的变化范围分别为12.91%~47.95%和14.21%~69.46%。相关分析表明:MBC、ROC和POC含量与土壤总有机碳(SOC)含量呈极显著正相关(P0.01),SOC、MBC、ROC和POC含量与全氮、全磷及碳氮比呈极显著正相关(P0.01)。研究结果为了解白桦林在演替过程中土壤有机碳的稳定性变化和固碳潜力提供数据支持。