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91.
92.
铁是植物生长发育的必需元素。由于土壤中的三价铁离子不能被植物直接利用, 使一些植物经常表现出缺铁症状。为探讨利用铁蛋白基因提高植物耐低铁胁迫的作用, 利用农杆菌介导法将大豆铁蛋白基因SoyFer1和内源反义铁蛋白基因NtFer2的cDNA分别导入烟草基因组, 采集转基因烟草种子。对T1转基因烟草的卡那霉素抗性分析表明, 整合到烟草基因组的外源基因多为单拷贝基因, 也有少数为多拷贝基因。对具有卡那霉素抗性的转基因植株进行PCR检测和Northern杂交分析表明, 外源基因已整合到烟草基因组中, 并且得到了正确表达。将转基因株系移栽到铁离子浓度不同的培养基中生长2个月后进行比较表明, 转大豆铁蛋白基因烟草株系的生长量明显高于非转基因烟草株系, 而转内源反义铁蛋白基因烟草株系的生长量则明显低于非转基因烟草株系。转大豆铁蛋白基因和转内源反义铁蛋白基因烟草株系的叶绿素含量、丙二醛(MDA)含量和过氧化物酶(POD)活性等生理性状也发生了明显变化, 表现为转大豆铁蛋白基因株系的叶绿素含量明显增加, POD活性明显增强, MDA含量明显降低; 而转内源反义铁蛋白基因株系的叶绿素含量、POD活性和MDA含量等则表现为与转大豆铁蛋白基因株系的相反。铁蛋白过量表达提高了烟草耐低铁能力, 而铁蛋白抑制表达则降低了烟草耐低铁能力。 相似文献
93.
Four different ratios of river sand, ceramic pellets, vermiculite and perlite (1:1), and field soil were selected as the
substrates in this experiment, and four gradient levels of root waterlogging, half waterlogging, full waterlogging
and normal were set to investigate the effects of different gradients of waterlogging stress on the root morphology
of Taxus chinensis var. mairei seedlings under different substrates. In this study, the root anatomical structure of
Taxus chinensis var. mairei under different waterlogging stress was observed by the paraffin section method. The
roots of T. chinensis var. mairei were diarch, with no pith and resin canals. There was a large number of tannins in
the pericycle of the aerial adventitious roots of seedlings adapted to waterlogging. Also, the endodermis has
obvious casparian strip thickening, and there were 4-5 layers of large parenchymatous cells in the close to the
inner side of the pericycle in the vascular cylinder, which could increase the storage capacity, and transport capacity of the root. Under the treatment of root waterlogging stress, the development of plant roots in the mixed
substrate of vermiculite and, perlite was the earliest. Under half waterlogging stress, T. chinensis var. mairei seedlings treated with various substrates all could better adapt to the environment of waterlogging stress. Under the
stress of fully waterlogging, the roots of seedlings planted in river sand substrate developed secondary growth. 相似文献
94.
基于集中参数模型的脑血管疾病数值模拟 总被引:3,自引:0,他引:3
脑血管疾病的血流动力研究一直是和脑血管疾病的预防和诊断密切相关的,由于脑部血流循环是一个四端输入的网络,其复杂性导致它的血液动力学规律和体循环有着本质的差别,讨论脑循环这模型和临床应用有着重要的意义,本文使用集中参数模型来模拟三种常见的脑血管疾病;脑动脉硬化,脑梗塞,锁骨下动脉盗血,考察其对相应脑血管的压力和流量的影响,结果显示脑部血液循环的代偿功能在发病情况下的重要作用,本文通过分析数值模拟结果,对不同疾病的血液动力学特征进行研究,给脑血管疾病的临床诊断提供血液动力学方面的参考。 相似文献
95.
Jiaming Tian Bingxin Dai Li Gong Pingping Wang Han Ding Siwei Xia Weice Sun Cuiping Ren Jijia Shen Miao Liu 《PLoS neglected tropical diseases》2022,16(8)
Schistosomiasis is a serious and widespread parasitic disease caused by infection with Schistosoma. Because the parasite’s eggs are primarily responsible for schistosomiasis dissemination and pathogenesis, inhibiting egg production is a potential approach to control the spread and severity of the disease. The bromodomain and extra-terminal (BET) proteins represent promising targets for the development of epigenetic drugs against Schistosoma. JQ-1 is a selective inhibitor of the BET protein family. In the present study, JQ-1 was applied to S. japonicum in vitro. By using laser confocal scanning microscopy and EdU incorporation assays, we showed that application of JQ-1 to worms in vitro affected egg laying and the development of both the male and female reproductive systems. JQ-1 also inhibited the expression of the reproductive-related genes SjPlk1 and SjNanos1 in S. japonicum. Mice infected with S. japonicum were treated with JQ-1 during egg granuloma formation. JQ-1 treatment significantly reduced the size of the liver granulomas and levels of serum alanine aminotransferase and aspartate aminotransferase in mice and suppressed both egg laying and the development of male and female S. japonicum reproductive systems in vivo. Moreover, the mRNA expression levels of some proinflammatory cytokines were decreased in the parasites. Our findings suggest that JQ-1 treatment attenuates S. japonicum egg–induced hepatic granuloma due at least in part to suppressing the development of the reproductive system and egg production of S. japonicum. These findings further suggest that JQ-1 or other BET inhibitors warrant additional study as a new approach for the treatment or prevention of schistosomiasis. 相似文献
96.
Andi Zhang Yi Pan Hao Wang Rui Ding Tianyuan Zou Dongye Guo Yilin Shen Peilin Ji Weiyi Huang Qing Wen Quan Wang Haixia Hu Jichang Wu Mingliang Xiang Bin Ye 《Aging cell》2024,23(4):e14091
The pathogenesis of age-related hearing loss (ARHL) remains unclear. OPA1 is the sole fusion protein currently known to be situated in the inner mitochondrial membrane, which is pivotal for maintaining normal mitochondrial function. While it has already been demonstrated that mutations in OPA1 may lead to hereditary deafness, its involvement in the occurrence and development of ARHL has not been previously explored. In our study, we constructed D-gal-induced senescent HEI-OC1 cells and the cochlea of C57BL/6J mice with a mutated SUMOylation site of SIRT3 using CRISPR/Cas9 technology. We found enhanced L-OPA1 processing mediated by activated OMA1, and increased OPA1 acetylation resulting from reductions in SIRT3 levels in senescent HEI-OC1 cells. Consequently, the fusion function of OPA1 was inhibited, leading to mitochondrial fission and pyroptosis in hair cells, ultimately exacerbating the aging process of hair cells. Our results suggest that the dysregulation of mitochondrial dynamics in cochlear hair cells in aged mice can be ameliorated by activating the SIRT3/OPA1 signaling. This has the potential to alleviate the senescence of cochlear hair cells and reduce hearing loss in mice. Our study highlights the significant roles played by the quantities of long and short chains and the acetylation activity of OPA1 in the occurrence and development of ARHL. This finding offers new perspectives and potential targets for the prevention and treatment of ARHL. 相似文献
97.
Yukun Xiao Meng Wang Haozhou Yang Haoran Qiu Haotian Lu Yumin Da Ganwen Chen Tianyuan Jiang Weiwei Fu Bihao Hu Junmei Chen Lei Chen Yishui Ding Baihua Cui Chonglai Jiang Zejun Sun Yu Long Haotian Yang Zhangliu Tian Lei Wang Wei Chen 《Liver Transplantation》2024,14(1):2302556
Electrocatalytic CO2 reduction (CO2R) coupled with renewable electricity has been considered as a promising route for the sustainability transition of energy and chemical industries. However, the unsatisfactory yield of desired products, particularly multicarbon (C2+) products, has hindered the implementation of this technology. This work describes a strategy to enhance the yield of C2+ product formation in CO2R by utilizing spatial confinement effects. The finite element simulation results suggest that increasing the number of shells in the catalyst wil lead to a high local concentration of *CO and promotes the formation of C2+ products. Inspired by this, Cu nanoparticles are synthesized with desired hollow multi-shell structures. The CO2 reduction results confirm that as the number of shells increase, the hollow multi-shell copper catalysts exhibit improved selectivity toward C2+ products. Specifically, the Cu catalyst with 4.4-shell achieved a high selectivity of over 80% toward C2+ at a current density of 900 mA cm−2. Evidence from in situ attenuated total reflection surface-enhanced infrared absorption spectroscopy unveils that the multi-shell Cu catalyst exhibits an enhanced *COatop coverage and the stronger interaction with *COatop compared to commercial Cu, confirming the simulation results. Overall, the work promises an effective approach for boosting CO2R selectivity toward value-added chemicals. 相似文献
98.
Till Ortmann Till Fuchs Janis K. Eckhardt Ziming Ding Qianli Ma Frank Tietz Christian Kübel Marcus Rohnke Jürgen Janek 《Liver Transplantation》2024,14(15):2302729
“Anode-free” solid-state battery concepts are explored extensively as they promise a higher energy density with less material consumption and simple anode processing. Here, the homogeneous and uniform electrochemical deposition of alkali metal at the interface between current collector and solid electrolyte plays the central role to form a metal anode within the first cycle. While the cathodic deposition of lithium has been studied intensively, knowledge on sodium deposition is scarce. In this work, dense and uniform sodium layers of several microns thickness are deposited at the Cu|Na3.4Zr2Si2.4P0.6O12 interface with high reproducibility. At current densities of ≈1 mA∙cm−2, relatively uniform coverage is achieved underneath the current collector, as shown by electrochemical impedance spectroscopy and 3D confocal microscopy. In contrast, only slight variations of the coverage are observed at different stack pressures. Early stages of the sodium metal growth are analyzed by in situ transmission electron microscopy revealing oriented growth of sodium. The results demonstrate that reservoir-free (“anode-free”) sodium-based batteries are feasible and may stimulate further research efforts in sodium-based solid-state batteries. 相似文献
99.
Yu'e Liu Yihong Sun Yadong Guo Xiaoyun Shi Xi Chen Wenfeng Feng Lei-Lei Wu Jin Zhang Shibo Yu Yi Wang Yufeng Shi 《International journal of biological sciences》2023,19(3):897
Mitochondria are intracellular organelles involved in energy production, cell metabolism and cell signaling. They are essential not only in the process of ATP synthesis, lipid metabolism and nucleic acid metabolism, but also in tumor development and metastasis. Mutations in mtDNA are commonly found in cancer cells to promote the rewiring of bioenergetics and biosynthesis, various metabolites especially oncometabolites in mitochondria regulate tumor metabolism and progression. And mutation of enzymes in the TCA cycle leads to the unusual accumulation of certain metabolites and oncometabolites. Mitochondria have been demonstrated as the target for cancer treatment. Cancer cells rely on two main energy resources: oxidative phosphorylation (OXPHOS) and glycolysis. By manipulating OXPHOS genes or adjusting the metabolites production in mitochondria, tumor growth can be restrained. For example, enhanced complex I activity increases NAD+/NADH to prevent metastasis and progression of cancers. In this review, we discussed mitochondrial function in cancer cell metabolism and specially explored the unique role of mitochondria in cancer stem cells and the tumor microenvironment. Targeting the OXPHOS pathway and mitochondria-related metabolism emerging as a potential therapeutic strategy for various cancers. 相似文献
100.
Bing-xin Sun Ai-shi Peng Pei-jie Liu Min-jia Wang Hai-li Ding Yu-shi Hu Liang Kang 《Purinergic signalling》2023,19(1):297
The neurotrophin brain-derived neurotrophic factor (BDNF), which acts as a transducer, is responsible for improving cerebral stroke, neuropathic pain, and depression. Exercise can alter extracellular nucleotide levels and purinergic receptors in central nervous system (CNS) structures. This inevitably activates or inhibits the expression of BDNF via purinergic receptors, particularly the P2X receptor (P2XR), to alleviate pathological progression. In addition, the significant involvement of sensitive P2X4R in mediating increased BDNF and p38-MAPK for intracerebral hemorrhage and pain hypersensitivity has been reported. Moreover, archetypal P2X7R blockade induces mouse antidepressant-like behavior and analgesia by BDNF release. This review summarizes BDNF-mediated neural effects via purinergic receptors, speculates that P2X4R and P2X7R could be priming molecules in exercise-mediated changes in BDNF, and provides strategies for the protective mechanism of exercise in neurogenic disease. 相似文献