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排序方式: 共有127条查询结果,搜索用时 31 毫秒
101.
Masoud Najafi Nasser Hashemi Goradel Bagher Farhood Eniseh Salehi Maryam Shabani Nashtaei Neda Khanlarkhani Zahra Khezri Jamal Majidpoor Morteza Abouzaripour Mohsen Habibi Iraj Ragerdi Kashani Keywan Mortezaee 《Journal of cellular biochemistry》2019,120(3):2756-2765
Macrophages are the most abundant cells within the tumor stroma displaying noticeable plasticity, which allows them to perform several functions within the tumor microenvironment. Tumor-associated macrophages commonly refer to an alternative M2 phenotype, exhibiting anti-inflammatory and pro-tumoral effects. M2 cells are highly versatile and multi-tasking cells that directly influence multiple steps in tumor development, including cancer cell survival, proliferation, stemness, and invasiveness along with angiogenesis and immunosuppression. M2 cells perform these functions through critical interactions with cells related to tumor progression, including Th2 cells, cancer-associated fibroblasts, cancer cells, regulatory T cells (Tregs), and myeloid-derived suppressor cells. M2 cells also have negative cross-talks with tumor suppressor cells, including cytotoxic T cells and natural killer cells. Programed death-1 (PD-1) is one of the key receptors expressed in M2 cells that, upon interaction with its ligand PD-L1, plays cardinal roles for induction of immune evasion in cancer cells. In addition, M2 cells can neutralize the effects of the pro-inflammatory and anti-tumor M1 phenotype. Classically activated M1 cells express high levels of major histocompatibility complex molecules, and the cells are strong killers of cancer cells. Therefore, orchestrating M2 reprogramming toward an M1 phenotype would offer a promising approach for reversing the fate of tumor and promoting cancer regression. Macrophage switching toward an anti-inflammatory M1 phenotype could be used as an adjuvant with other approaches, including radiotherapy and immune checkpoint blockades, such as anti-PD-L1/PD-1 strategies. 相似文献
102.
Elahe Seyed Hosseini Rezvan Moniri Yasaman Dasteh Goli Hamed Haddad Kashani 《Probiotics and antimicrobial proteins》2016,8(4):202-210
Therapeutic LysK-CHAP is a potent anti-staphylococcal protein that could be utilized as an antibiotic substitute. Intein-mediated protein purification is a reasonable and cost-effective method that is most recently used for recombinant therapeutic protein production. Intein (INT) is the internal parts of the protein that can be separated from the immature protein during protein splicing process. This sequence requires no specific enzyme or cofactor for separation. INT sequence and their characteristic of self-cleavage by thiol induction, temperature, and pH changes are used for protein purification. The current study presents the expression of CHAPK262 domain of LysK gene that is fused with INT/chitin-binding sequence while evaluating its purification procedure and antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA). The coding gene sequence of LysK-CHAP (CHAPK262) in pET22-b was amplified with polymerase chain reaction (PCR); the digested product was then cloned into the pTXB1 vector. Electrophoresis confirmed the cloning accuracy of the gene. The pTXB1-CHAPK262 plasmid was transformed to the Escherichia coli ER2566 (E. coli ER2566) expression strain and analyzed for expression of the recombinant protein by SDS-PAGE and Western blotting methods. Finally, CHAPK262 was purified by chitin affinity column using INT tag technology and confirmed by SDS-PAGE. Lytic activity of the purified protein was investigated by disk diffusion method. Cloning of CHAPK262 into the pTXB1 vector, which comprised INT/chitin-binding sequence, was successfully achieved. The SDS-PAGE data also revealed successful expression of the CHAPK262-INT fusion protein and Western blotting method validated the accuracy of the protein. Moreover, purification of CHAPK262 protein was induced by dithiothreitol (DTT) and confirmed by SDS-PAGE. Finally, inhibition zone in MRAS culture medium confirmed antibacterial activity of the protein. Application of intein-mediated antibacterial protein is an appropriate and streamlined method for one-step purification of CHAPK262 as a therapeutic and antibacterial protein. Self-cleaving tags like intein are cost-effective and could be used as a proper purification method for industrial purposes. 相似文献
103.
Rasha AH Attia Abeer E Mahmoud Haiam Mohammed Mahmoud Farrag Rania Makboul Mona Embarek Mohamed Zedan Ibraheim 《Memórias do Instituto Oswaldo Cruz》2015,110(8):1035-1041
Trichinellosis is a serious disease with no satisfactory treatment. We aimed to
assess the effect of myrrh (Commiphora molmol) and, for the first
time, thyme (Thymus vulgaris L.) against enteral
and encysted (parenteral) phases of Trichinella spiralis in mice
compared with albendazole, and detect their effect on inducible nitric oxide synthase
(iNOS) expression. Oral administration of 500 mg/kg of myrrh and thyme led to adult
reduction (90.9%, 79.4%), while 1,000 mg/kg led to larvae reduction (79.6%, 71.3%),
respectively. Administration of 50 mg/kg of albendazole resulted in adult and larvae
reduction (94.2%, 90.9%). Positive immunostaining of inflammatory cells infiltrating
intestinal mucosa and submucosa of all treated groups was detected. Myrrh-treated
mice showed the highest iNOS expression followed by albendazole, then thyme. On the
other hand, both myrrh and thyme-treated groups showed stronger iNOS expression of
inflammatory cells infiltrating and surrounding encapsulated T.
spiralis larvae than albendazole treated group. In conclusion, myrrh and
thyme extracts are highly effective against both phases of T.
spiralis and showed strong iNOS expressions, especially myrrh which could
be a promising alternative drug. This experiment provides a basis for further
exploration of this plant by isolation and retesting the active principles of both
extracts against different stages of T. spiralis. 相似文献
104.
Blocking the QB‐binding site of photosystem II by tenuazonic acid,a non–host‐specific toxin of Alternaria alternata,activates singlet oxygen‐mediated and EXECUTER‐dependent signalling in Arabidopsis
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SHIGUO CHEN CHANHONG KIM JE MIN LEE HYUN‐AH LEE ZHANGJUN FEI LIANGSHENG WANG KLAUS APEL 《Plant, cell & environment》2015,38(6):1069-1080
Necrotrophic fungal pathogens produce toxic compounds that induce cell death in infected plants. Often, the primary targets of these toxins and the way a plant responds to them are not known. In the present work, the effect of tenuazonic acid (TeA), a non–host‐specific toxin of Alternaria alternata, on Arabidopsis thaliana has been analysed. TeA blocks the QB‐binding site at the acceptor side of photosystem II (PSII). As a result, charge recombination at the reaction centre (RC) of PSII is expected to enhance the formation of the excited triplet state of the RC chlorophyll that promotes generation of singlet oxygen (1O2). 1O2 activates a signalling pathway that depends on the two EXECUTER (EX) proteins EX1 and EX2 and triggers a programmed cell death response. In seedlings treated with TeA at half‐inhibition concentration 1O2‐mediated and EX‐dependent signalling is activated as indicated by the rapid and transient up‐regulation of 1O2‐responsive genes in wild type, and its suppression in ex1/ex2 mutants. Lesion formation occurs when seedlings are exposed to higher concentrations of TeA for a longer period of time. Under these conditions, the programmed cell death response triggered by 1O2‐mediated and EX‐dependent signalling is superimposed by other events that also contribute to lesion formation. 相似文献
105.
Six species of terrestrial isopods from the province of Qazvin, central Iran, are recorded. Three species, Hemilepistus
klugii (Brandt, 1833), Protracheoniscus
ehsani Kashani, 2014 and Mongoloniscus
persicus Kashani, 2014, were previously reported from the province. Hemilepistus
elongatus Budde-Lund, 1885 and Protracheoniscus
major (Dollfus, 1903) are recorded for the first time, and one species, Protracheoniscus
sarii
sp. n., is described as new. The diagnostic characters of the new species are figured. 相似文献
106.
107.
The authors propose an effective technique to isolate whole, intact vitreous core and cortex from post mortem enucleated porcine eyes. While previous studies have shown the results of such dissections, the detailed steps have not been described, precluding researchers outside the field from replicating their methods. Other studies harvest vitreous either through aspiration, which does not maintain the vitreous structure anatomy, or through partial dissection, which only isolates the vitreous core. The proposed method isolates the whole vitreous body, with the vitreous core and cortex intact, while maintaining vitreous anatomy and structural integrity. In this method, a full thickness scleral flap in an enucleated porcine eye is first created and through this, the choroid tissue can be separated from the sclera. The scleral flap is then expanded and the choroid is completely separated from the sclera. Finally the choroid-retina tissue is peeled off the vitreous to leave an isolated intact vitreous body. The proposed vitreous dissection technique can be used to study physical properties of the vitreous humor. In particular, this method has significance for experimental studies involving drug delivery, vitreo-retinal oxygen transport, and intraocular convection. 相似文献
108.
Differences in single-copy nuclear-DNA sequences among 13 species of
passerine birds were measured using DNA-DNA hybridization. A matrix of
pairwise dissimilarity values (delta mode distances) was constructed from
analysis of fitted thermal dissociation curves. A least-squares method of
phylogenetic estimation was used to construct two topologies from the
distance matrix, one constraining branch lengths of sister taxa to be equal
and the other permitting such lengths to vary. These topologies were
identical in the pattern of branching of taxa, and the difference in their
sums of squares was not statistically significant, suggesting that rates of
DNA evolution in sister groups of nine- primaried oscines are equal. A
nonparametric test for nonrandom variation in distances of sister groups to
outgroup taxa revealed no statistically significant deviation from random
variation that would be expected as a result of measurement error. However,
the level of measurement error was such that rates of DNA evolution in
sister taxa could vary by as much as 10% without being detected with the
statistical methods used here.
相似文献
109.
脑电信号数据压缩及棘波识别的小波神经网络方法 总被引:1,自引:0,他引:1
本文在对小波神经网络及其算法研究的基础上,提出了一种对脑电信号压缩表达和痫样脑电棘波识别的新方法。实验结果显示,小波网络在大量压缩数据的同时,能够较好的恢复原有信号,另外,在脑电信号的时频谱等高线图上,得到了易于自动识别的棘波和棘慢复合波特征,说明此方法在电生理信号处理和时频分析方面有着光明的应用前景。 相似文献
110.
14-3-3 proteins double the number of outward-rectifying K+ channels available for activation in tomato cells 总被引:1,自引:0,他引:1
Booij PP Roberts MR Vogelzang SA Kraayenhof R De Boer AH 《The Plant journal : for cell and molecular biology》1999,20(6):673-683
Outward-rectifying K+ channels are modulated in response to environmental stimuli by a range of intracellular factors, such as cytoplasmic Ca2+, pH, kinases and phosphatases. Here we report that voltage-dependent outward-rectifying K+ channels in tomato cells are also targets for modulation by 14-3-3 proteins. In whole-cell patch-clamp experiments, recombinant 14-3-3 protein (tomato isoform TFT7) was introduced into tomato cell protoplasts via the patch pipette. As a result the steady-state outward K+ current increased twofold and this increase was not dependent upon the presence of cytoplasmic ATP. A phosphorylated peptide that contained a phosphorylated 14-3-3 target-binding motif (RSTS*TP), derived from nitrate reductase, blocked the effect of 14-3-3, thus showing the specific nature of 14-3-3 action. Kinetic parameters of the conductance, like (de)activation kinetics, voltage dependence of gating and activation potential, were not significantly different between control and 14-3-3 infused cells. Analysis of single-channel activity and whole-cell noise indicated that the single-channel conductance was not affected by 14-3-3 infusion. We conclude that 14-3-3 proteins recruit 'sleepy' channels into a voltage-activatable state. The molecular mechanism underlying the 1 : 1 ratio of constitutively active and 14-3-3 recruited channels is discussed in the light of known functions of 14-3-3 dimers. 相似文献