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Further Evidence for Multiple Forms of an N-Methyl-d-Aspartate Recognition Domain in Rat Brain Using Membrane Binding Techniques 总被引:1,自引:1,他引:0
Pingping Zuo Kiyokazu Ogita Takeo Suzuki Daiken Han Yukio Yoneda 《Journal of neurochemistry》1993,61(5):1865-1873
Abstract— Pretreatment with sulfhydryl-reactive agents, such as N-ethylmaleimide and p-chloromercuriphenylsul-fonic acid, invariably resulted in marked inhibition of the binding of dl -(E)-2-amino-4-[3H]propyl-5-phosphono-3-pentenoic acid ([3H]CGP 39653), a competitive antagonist at an N-methyl-d -aspartate (NMDA)-sensitive subclass of central excitatory amino acid receptors, in brain synaptic membranes extensively washed and treated with Triton X-100, but did not significantly affect the binding of L-[3H]-glutamic acid ([3H]Glu), an endogenous agonist. The pre-treatment was effective in reducing the binding of [3H]-CGP 39653 at equilibrium, without altering the initial association rate, and decreased the affinity for the ligand. Pretreatment with sulfhydryl-reactive agents also enhanced the potencies of NMDA agonists to displace [3H]-CGP 39653 binding and attenuated those of NMDA antagonists, but had little effect on the potencies of the agonists and antagonists to displace [3H]Glu binding. The binding of both [3H]CGP 39653 and [3H]Glu was similarly sensitive to pretreatment with four different proteases in Tritontreated membranes, whereas pretreatment with phospho-lipase A2 or C markedly inhibited [3H]CGP 39653 binding without altering [3H]Glu binding. Moreover, both phospho-lipases not only induced enhancement of the abilities of NMDA agonists to displace the binding of [3H]CGP 39653 and [3H]Glu, but also caused diminution of those of NMDA antagonists. These results suggest that both sulfhydryl-reactive agents and phospholipases may predominantly interfere with radiolabeling of the NMDA recognition domain in a state favorable to an antagonist by [3H]CGP 39653, with concomitant facilitation of that in an agonist-preferring form by [3H]Glu. The possible presence of multiple forms of the NMDA recognition domain is further supported by these data. 相似文献
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利用EB病毒转化可产生较高水平人IgG和特异性抗2型登革病毒人抗体的Hu-TLC-SCID小鼠脾细胞,通过免疫组化、免疫荧光和PCR法检测转化细胞的人B细胞表面标志、EB病毒抗原和EB病毒基因。结果表明,被转化的Hu-TLC-SCID小鼠脾细胞能继续产生抗2型登革病毒的特异性人抗体,并具有人B细胞的、SmIgG标志及EB病毒潜伏膜蛋白-1(LMP-1)基因,可表达LMP-1和EB病毒核抗原(EBNA)。 相似文献
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原生质体电融合酵母多倍体生理特性的研究 总被引:5,自引:0,他引:5
对原生质体电融合技术获得的11株酵母多倍体融合株,进行了一系列生理特性的分析比较.结果发现,在电融合过程中,融合株的细胞体积及DNA含量并不随着核倍性呈线性递增.而是有其特殊的变化规律。当糖化酵母sta1、sta2和sta3在细胞核中各自纯合时,明显表现出表达的剂量效应。其中sta1、sta2纯合的融合株.在YEPS培养中,GA分泌可被淀粉大量诱导,表现出一定的二次生长特性。从分析结果推测,在亲株5301-14D及HU-TY—1A中可能有对GA分泌不利的因素。 相似文献
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Paleolimnology of Qilu Hu,Yunnan Province,China 总被引:4,自引:0,他引:4
Mark Brenner Kathleen Dorsey Song Xueliang Wang Zuguan Long Ruihua Michael W. Binford Thomas J. Whitmore Allen M. Moore 《Hydrobiologia》1991,214(1):333-340
Qilu Hu is a large (A = 36.9 km2), shallow (zmax = 6.8 m) lake that lies at an elevation of 1797 m above msl on the Yunnan Plateau, southern China. Lake waters are hard (Mg = 3.2m eq L–1, Ca = 1.3 meq L–1 ), fresh (conductivity = 380 S cm –1), and productive (Secchi < 40 cm). An 11-m sediment core has a basal 14C age of 30960 ± 860 B.P. Sediments between 11 m and 6 m are high in % dry weight, rich in clay components Al2O3, Fe2O3, K2O, MgO, and low in organic C (6.1%), carbonate-C (<1.0%), total N (<3.2 mg g–1), and total S (<-1.7 mg g–1). Diatoms and pollen indicate open-water conditions between 9.0 m and 6.0 m (1342011790 B.P.). Above 6.0 m, CaCO3 and organic matter concentrations increase relative to clastics. The transition marks a change to shallow-water conditions as inferred from diatoms and pollen, and probably reflects a shift to drier climate. Uppermost (80-0 cm) red clays were deposited rapidly, probably as a consequence of recent (decades to centuries) riparian disturbances (e.g. agriculture, lake-bottom reclamation, urban development). Dates assigned to events in the Qilu Hu profile are tentative because of potential hard-water-lake error. 相似文献
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Wei Lv Wei Jiang Hongmei Luo Qian Tong Xiaoyu Niu Xiao Liu Yang Miao Jingnan Wang Yiwen Guo Jianan Li Xizhen Zhan Yunqing Hou Yaxin Peng Jian Wang Shuhong Zhao Zaiyan Xu Bo Zuo 《Nucleic acids research》2022,50(18):10733
Long noncoding RNAs (lncRNAs) play important roles in the spatial and temporal regulation of muscle development and regeneration. Nevertheless, the determination of their biological functions and mechanisms underlying muscle regeneration remains challenging. Here, we identified a lncRNA named lncMREF (lncRNA muscle regeneration enhancement factor) as a conserved positive regulator of muscle regeneration among mice, pigs and humans. Functional studies demonstrated that lncMREF, which is mainly expressed in differentiated muscle satellite cells, promotes myogenic differentiation and muscle regeneration. Mechanistically, lncMREF interacts with Smarca5 to promote chromatin accessibility when muscle satellite cells are activated and start to differentiate, thereby facilitating genomic binding of p300/CBP/H3K27ac to upregulate the expression of myogenic regulators, such as MyoD and cell differentiation. Our results unravel a novel temporal-specific epigenetic regulation during muscle regeneration and reveal that lncMREF/Smarca5-mediated epigenetic programming is responsible for muscle cell differentiation, which provides new insights into the regulatory mechanism of muscle regeneration. 相似文献
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Bo Li YuZhen Ge WeiWei Yan Bin Gong Kun Cao Rui Zhao Chao Li YeWei Zhang YiHeng Jiang Shi Zuo 《Cell proliferation》2022,55(9)
As a member of the deoxyribonuclease 1 family, DNASE1L3 plays a significant role both inside and outside the cell. However, the role of DNASE1L3 in hepatocellular carcinoma (HCC) and its molecular basis remains to be further investigated. In this study, we report that DNASE1L3 is downregulated in clinical HCC samples and evaluate the relationship between its expression and HCC clinical features. In vivo and in vitro experiments showed that DNASE1L3 negatively regulates the proliferation, invasion and metastasis of HCC cells. Mechanistic studies showed that DNASE1L3 recruits components of the cytoplasmic β‐catenin destruction complex (GSK‐3β and Axin), promotes the ubiquitination degradation of β‐catenin, and inhibits its nuclear transfer, thus, decreasing c‐Myc, P21 and P27 level. Ultimately, cell cycle and EMT signals are restrained. In general, this study provides new insight into the mechanism for HCC and suggests that DNASE1L3 can become a considerable target for HCC.Decreased expression of DNASE1L3 is associated with poor prognosis in patients with HCC DNASE1L3 inhibits the proliferation and cell cycle of HCC cells in vitro and promotes the invasion and metastasis of HCC cells DNASE1L3 inhibits the tumorigenicity and metastasis of HCC cells in vivo DNASE1L3 interacts with β‐catenin and promotes its binding to the β‐catenin destroying complex DNASE1L3 interacts with P21 and stabilizes P21 by mediating the deubiquitin activity 相似文献