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81.
Zahra Javanmardi Mahmoud Mahmoudi Houshang Rafatpanah Zahra Rezaieyazdi Abbas Shapouri-Moghaddam Parisa Ahmadi Samaneh Mollazadeh Nafiseh Sadat Tabasi Seyed-Alireza Esmaeili 《Cell biochemistry and function》2024,42(2):e3981
Systemic lupus erythematosus (SLE) is known as an autoimmune disorder that is characterized by the breakdown of self-tolerance, resulting in disease onset and progression. Macrophages have been implicated as a factor in the development of SLE through faulty phagocytosis of dead cells or an imbalanced M1/M2 ratio. The study aimed to investigate the immunomodulatory effects of Lactobacillus delbrueckii and Lactobacillus rhamnosus on M1 and M2 macrophages in new case lupus patients. For this purpose, blood monocytes were collected from lupus patients and healthy people and were cultured for 5 days to produce macrophages. For 48 h, the macrophages were then cocultured with either probiotics or lipopolysaccharides (LPS). Flow cytometry and real-time polymerase chain reaction were then used to analyze the expression of cluster of differentiation (CD) 14, CD80, and human leukocyte antigen – DR (HLADR) markers, as well as cytokine expression (interleukin [IL]1-β, IL-12, tumor necrosis factor α [TNF-α], IL-10, and transforming growth factor beta [TGF-β]). The results indicated three distinct macrophage populations, M0, M1, and M2. In both control and patient-derived macrophage-derived monocytes (MDMs), the probiotic groups showed a decrease in CD14, CD80, and HLADR expression compared to the LPS group. This decrease was particularly evident in M0 and M2 macrophages from lupus patients and M1 macrophages from healthy subjects. In addition, the probiotic groups showed increased levels of IL-10 and TGF-β and decreased levels of IL-12, IL1-β, and TNF-α in MDMs from both healthy and lupus subjects compared to the LPS groups. Although there was a higher expression of pro-inflammatory cytokines in lupus patients, there was a higher expression of anti-inflammatory cytokines in healthy subjects. In general, L. delbrueckii and L. rhamnosus could induce anti-inflammatory effects on MDMs from both healthy and lupus subjects. 相似文献
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Majid Ahmadi Mahnaz Ghaebi Samaneh Abdolmohammadi-Vahid Sanaz Abbaspour-Aghdam Kobra Hamdi Sedigheh Abdollahi-Fard Shahla Danaii Parisa Mosapour Ladan Koushaeian Sanam Dolati Reza Rikhtegar Farnaz Dabiri Oskouei Leili Aghebati-Maleki Mohammad Nouri Mehdi Yousefi 《Journal of cellular physiology》2019,234(6):9428-9437
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Plasmonics - Excitation of THz surface plasmons due to the scattering of transverse magnetic (TM) wave by an elliptical plasma antenna consisting of a metallic rod with dielectric coating is... 相似文献
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Molecular and Cellular Biochemistry - MicroRNAs (miRNAs) are important molecules which implicated in various processes, such as differentiation, development, cell survival, cell apoptosis and also... 相似文献
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Four derivatives of N-trimellitylimido-l-amino acid (4a–4d) were prepared by the reaction of trimellitic anhydride (1) with the l-amino acids (2a–2d) in acetic acid as diacid monomers and were used with the aim to obtain a new family of amino acid based poly(ester-imide)s (PEI)s. The polymerization was performed by direct polycondensation of chiral diacids (4a–4d) with 4,4′-thiobis(2-tert-butyl-5-methylphenol) (5) in the presence of tosyl chloride (TsCl), pyridine and N,N-dimethyl formamide (DMF). Step-growth polymerization was carried out by varying the time of heating and the molar ratio of TsCl/diacid and the optimum conditions were achieved. The synthesized polymers were characterized by means of specific rotation experiments, FT-IR, 1H-NMR, X-ray diffraction techniques and elemental analysis. The surface morphology of the obtained polymers was studied by field emission scanning electron microscopy. The result showed nanostructure morphology of the resulting polymers. The obtained PEIs were soluble in polar aprotic solvents such as DMF, N,N-dimethyl acetamide, dimethyl sulfoxide, N-methyl-2-pyrrolidone and protic solvents such as sulfuric acid. Thermal stability and the weight-loss behavior of the PEIs were studied by thermal gravimetric analysis (TGA) techniques. TGA showed that the 10% weight loss temperature in a nitrogen atmosphere was more than 402°C, therefore they had useful levels of thermal stability associated with excellent solubility. 相似文献
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Masoumeh Douraghi Samaneh Saberi Kashani Hojjat Zeraati Maryam Esmaili Akbar Oghalaie Marjan Mohammadi 《Current microbiology》2010,60(4):254-262
Helicobacter pylori, a microaerophilic fastidious bacterium, has been cultured on various plating and broth media since its discovery. Although
the agar media can be sufficient for the identification, typing, and antibiotic resistance studies, no secretory antigen of
H. pylori can be evaluated in such media. Thus, satisfactory growth of H. pylori in liquid culture which is needed for analysis of secretory proteins without the presence of interfering agents is in demand.
We assessed the impact of β-cyclodextrin, Fetal Bovine Serum (FBS), and charcoal as supplements for H. pylori growth. Furthermore, we aimed to identify the most favorable supplement that supports the secretion of the dominant secretory
protein, vacuolating cytotoxin (VacA). Five clinical strains were cultured on broth media and the growth, viability, morphology,
and protein content of each strain were determined. Our results revealed that β-cyclodextrin supports the growth rate, viability,
and cell lysate protein content to the extent similar to FBS. Application of β-cyclodextrin is found to postpone spiral to
coccoid conversion up to 72 h of incubation. Although FBS supports a higher VacA protein content, presence of interfering
macromolecules in FBS questions its utility particularly for purposes of studying extra cellular proteins such as VacA. This
study recommends further application of β-cyclodextrin as a culture supplement with the potential capacity in neutralizing toxic compounds and flourishing the secretion
of H. pylori proteins without addition of interfering proteins. 相似文献
88.
The mobility of heavy metals in contaminated soils is dependent on the kinetics release from soils. Metal extraction over time is commonly used to distinguish two or more fractions of metal based on differences of extraction or release rates. Kinetic studies using 0.01 M CaCl2, 0.01 M malic acid, and 0.01 M EDTA extractions were performed to characterize nickel (Ni) and lead (Pb) kinetic release in 10 contaminated calcareous soils. Proportions of Ni and Pb extracted with EDTA were higher than when using malic acid and CaCl2, respectively. The release of Ni and Pb was characterized by an initial fast rate followed by a slower rate and could best be described by a two first-order reactions model with rate constants k1 and k2 and two metal pools: readily labile (Q 1) and less labile (Q 2). In an EDTA extractant, different Q1 /Q2 ratios for Ni and Pb were observed, indicating binding energies to soil constituents is not comparable. The k1 of the model for Ni (average of 10 soils: 0.2204 h?1 and 0.2359 h?1 for 0.01 M CaCl2 and 0.01 EDTA, respectively) was higher than Pb (0.1044 h?1 and 0.1631 h?1 for 0.01 M CaCl2 and 0.01 M EDTA, respectively), indicating a higher potential of Ni for leaching and groundwater contamination in contaminated calcareous soils. Relationships between the fraction of Ni and Pb determined with the two first-order reactions model and the soil composition and Pb fractions were established. The results indicated that the efficiency of the extractions Ni and Pb from soils depends both on the Ni and Pb content and soil composition. Overall, the results indicated that the use of a 0.01 M malic acid washing solution would be preferred in the field condition. 相似文献
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William G Thilly Elena V Gostjeva Vera V Koledova Lawrence R Zukerberg Daniel Chung Janna N Fomina Firouz Darroudi B David Stollar 《Organogenesis》2014,10(1):44-52
Bell shaped nuclei of metakaryotic cells double their DNA content during and after symmetric and asymmetric amitotic fissions rather than in the separate, pre-mitotic S-phase of eukaryotic cells. A parsimonious hypothesis was tested that the two anti-parallel strands of each chromatid DNA helix were first segregated as ssDNA-containing complexes into sister nuclei then copied to recreate a dsDNA genome. Metakaryotic nuclei that were treated during amitosis with RNase A and stained with acridine orange or fluorescent antibody to ssDNA revealed large amounts of ssDNA. Without RNase treatment metakaryotic nuclei in amitosis stained strongly with an antibody complex specific to dsRNA/DNA. Images of amitotic figures co-stained with dsRNA/DNA antibody and DAPI indicated that the entire interphase dsDNA genome (B-form helices) was transformed into two dsRNA/DNA genomes (A-form helices) that were segregated in the daughter cell nuclei then retransformed into dsDNA. As this process segregates DNA strands of opposite polarity in sister cells it hypothetically offers a sequential switching mechanism within the diverging stem cell lineages of development. 相似文献
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