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981.
Differential role of microenvironment in microencapsulation for improved cell tolerance to stress 总被引:6,自引:0,他引:6
Sun ZJ Lv GJ Li SY Yu WT Wang W Xie YB Ma X 《Applied microbiology and biotechnology》2007,75(6):1419-1427
The effect of the microenvironment in alginate–chitosan–alginate (ACA) microcapsules with liquid core (LCM) and solid core
(SCM) on the physiology and stress tolerance of Sacchromyces cerevisiae was studied. The suspended cells were used as control. Cells cultured in liquid core microcapsules showed a nearly twofold
increase in the intracellular glycerol content, trehalose content, and the superoxide dismutase (SOD) activity, which are
stress tolerance substances, while SCM did not cause the significant physiological variation. In accordance with the physiological
modification after being challenged with osmotic stress (NaCl), oxidative stress (H2O2), ethanol stress, and heat shock stress, the cell survival in LCM was increased. However, SCM can only protect the cells
from damaging under ethanol stress. Cells released from LCM were more resistant to hyperosmotic stress, oxidative stress,
and heat shock stress than cells liberated from SCM. Based on reasonable analysis, a method was established to estimate the
effect of microenvironment of LCM and SCM on the protection of cells against stress factors. It was found that the resistance
of LCM to hyperosmotic stress, oxidative stress, and heat shock stress mainly depend on the domestication effect of LCM’s
microenvironment. The physical barrier of LCM constituted by alginate–chitosan membrane and liquid alginate matrix separated
the cells from the damage of oxidative stress and ethanol stress. The significant tolerance against ethanol stress of SCM
attributed to the physical barrier consists of solid alginate–calcium matrix and alginate–chitosan membrane. 相似文献
982.
The biological effects of rare-earth ions on the organism have been studied using Pr3+ as a probe ion and Escherichia coli cell as a target. Atomic force microscopy (AFM) observation of the surface of E. coli cells shows that the presence of Pr3+ substantially changes the structure of the outer membrane. By induced coupled plasma-mass spectrometry (ICP-MS), more Cu2+ was found in the cells grown in the presence of Pr3+, indicating changes of cell permeability. Using energy dispersive X-ray spectroscopy (EDX), Ca2+ is found on the outer surface of the original cell. It is proposed that Pr3+ can replace Ca2+ from the binding sites because of their close ionic radii and similar ligand speciality. 相似文献
983.
984.
A cytoplasmic NADH oxidase (NOX) was purified from a soil bacteria, Brevibacterium sp. KU1309, which is able to grow in the medium containing 2-phenylethanol as the sole source of carbon under an aerobic condition. The enzyme catalyzed the oxidation of NADH to NAD+ involving two-electron reduction of O2 to H2O2. The molecular weight of the enzyme was estimated to be 102 kDa by gel filtration and 57 kDa by SDS-PAGE, which indicates that the NOX was a homodimer consisting of a single subunit. The enzyme was stable up to 70 degrees C at a broad range of pH from 7 to 11. The enzyme activity increased about ten-fold with the addition of ammonium salt, while it was inhibited by Zn2+ (39%), Cu2+ (41%), Hg2+ (72%) and Ag+ (37%). The enzyme acts on NADH, but not on NADPH. The regeneration of NAD+ utilizing this enzyme made selective oxidation of mandelic acid or L: -phenylalanine possible. This thermostable enzyme is expected to be applicable as a useful biocatalyst for NAD+ recycling. 相似文献
985.
Hadley KC Borrelli MJ Lepock JR McLaurin J Croul SE Guha A Chakrabartty A 《Cell stress & chaperones》2011,16(5):549-561
The inability of cells to maintain protein folding homeostasis is implicated in the development of neurodegenerative diseases,
malignant transformation, and aging. We find that multiphoton fluorescence imaging of 1-anilinonaphthalene-8-sulfonate (ANS)
can be used to assess cellular responses to protein misfolding stresses. ANS is relatively nontoxic and enters live cells
and cells or tissues fixed in formalin. In an animal model of Alzheimer’s disease, ANS fluorescence imaging of brain tissue
sections reveals the binding of ANS to fibrillar deposits of amyloid peptide (Aβ) in amyloid plaques and in cerebrovascular
amyloid. ANS imaging also highlights non-amyloid deposits of glial fibrillary acidic protein in brain tumors. Cultured cells
under normal growth conditions possess a number of ANS-binding structures. High levels of ANS fluorescence are associated
with the endoplasmic reticulum (ER), Golgi, and lysosomes—regions of protein folding and degradation. Nuclei are virtually
devoid of ANS binding sites. Additional ANS binding is triggered by hyperthermia, thermal lesioning, proteasome inhibition,
and induction of ER stress. We also use multiphoton imaging of ANS binding to follow the in vivo recovery of cells from protein-damaging
insults over time. We find that ANS fluorescence tracks with the binding of the molecular chaperone Hsp70 in compartments
where Hsp70 is present. ANS highlights the sensitivity of specific cellular targets, including the nucleus and particularly
the nucleolus, to thermal stress and proteasome inhibition. Multiphoton imaging of ANS binding should be a useful probe for
monitoring protein misfolding stress in cells. 相似文献
986.
Michael Denker Alexa Riehle Markus Diesmann Sonja Grün 《Journal of computational neuroscience》2010,29(3):599-613
The hypothesis that cortical networks employ the coordinated activity of groups of neurons, termed assemblies, to process
information is debated. Results from multiple single-unit recordings are not conclusive because of the dramatic undersampling
of the system. However, the local field potential (LFP) is a mesoscopic signal reflecting synchronized network activity. This
raises the question whether the LFP can be employed to overcome the problem of undersampling. In a recent study in the motor
cortex of the awake behaving monkey based on the locking of coincidences to the LFP we determined a lower bound for the fraction
of spike coincidences originating from assembly activation. This quantity together with the locking of single spikes leads
to a lower bound for the fraction of spikes originating from any assembly activity. Here we derive a statistical method to
estimate the fraction of spike synchrony caused by assemblies—not its lower bound—from the spike data alone. A joint spike
and LFP surrogate data model demonstrates consistency of results and the sensitivity of the method. Combining spike and LFP
signals, we obtain an estimate of the fraction of spikes resulting from assemblies in the experimental data. 相似文献
987.
Background
In the past decades the rapid growth of molecular diagnostics (based on either traditional PCR or isothermal amplification technologies) meet the demand for fast and accurate testing. Although isothermal amplification technologies have the advantages of low cost requirements for instruments, the further improvement on sensitivity, speed and robustness is a prerequisite for the applications in rapid pathogen detection, especially at point-of-care diagnostics. Here, we describe and explore several strategies to improve one of the isothermal technologies, helicase-dependent amplification (HDA). 相似文献988.
Biological role of MicroRNA-103 based on expression profile and target genes analysis in pigs 总被引:1,自引:0,他引:1
MicroRNAs (miRNAs) are endogenously expressed RNAs consisting of 20–24 nucleotides. These molecules are thought to repress
protein translation by binding to target mRNAs. However, biological functions have not been assigned to most of the 175 porcine
miRNAs registered in miRBase (release 15.0). In an effort to uncover miR-103 important in pigs, we examined the integrative
tissue expression profile and gene ontology (GO) term enrichment of predicted target genes to determine the global biological
functions of miR-103. Our results demonstrated that miR-103 is involved in various biological processes including brain development,
lipid metabolism, adipocyte differentiation, hematopoiesis, and immunity. Moreover, we also experimentally verified effects
of miR-103 in porcine preadipocytes. miR-103 levels increased in differentiating adipocytes, and inhibition of miR-103 effectively
inhibited preadipocyte differentiation. In addition, mRNA levels of the putative miR-103 target RAI14 were higher in miR-103 inhibitor-treated adipocytes. These results demonstrate that miR-103 is involved in porcine preadipocyte
differentiation and may act through the putative target gene RAI14. In a word, our data provide new insights into the global biological role of miR-103. 相似文献
989.
Cell fusions are important to fertilization, placentation, development of skeletal muscle and bone, calcium homeostasis and
the immune defense system. Additionally, cell fusions participate in tissue repair and may be important to cancer development
and progression. A large number of factors appear to regulate cell fusions, including receptors and ligands, membrane domain
organizing proteins, proteases, signaling molecules and fusogenic proteins forming alpha-helical bundles that bring membranes
close together. The syncytin family of proteins represent true fusogens and the founding member, syncytin-1, has been documented
to be involved in fusions between placental trophoblasts, between cancer cells and between cancer cells and host cells. We
review the literature with emphasis on the syncytin family and propose that syncytins may represent universal fusogens in
primates and rodents, which work together with a number of other proteins to regulate the cell fusion machinery. 相似文献
990.
Allister EM Pal S Thomson AM Helmerhorst E Mamo JC 《Journal of biomedical science》2004,11(6):789-798
We compared the acute effect of insulin on the human colonic intestinal epithelial cell line CaCo-2 and the transformed human hepatic cell line HepG2. Over 24 h, 100 nM and 10 µM insulin significantly inhibited the secretion of apolipoprotein (apo) B-100 from HepG2 cells to 63 and 49% of control, respectively. Insulin had no effect on the secretion of apoB-48 from CaCo-2 cells. There was no effect of insulin on the cholesterol ester or free cholesterol concentrations in HepG2 or CaCo-2 cells. HepG2 and CaCo-2 cells bound insulin with high affinity, leading to similar stimulation of insulin receptor protein tyrosine kinase activation. Protein kinase C or mitogen-activated protein kinase activity in the presence or absence of insulin was not correlated with apoB-48 production in CaCo-2 cells. Therefore, insulin acutely decreases the secretion of apoB-100 in hepatic HepG2 cells, but does not acutely modulate the production or secretion of apoB-48 from CaCo-2 intestinal cells. 相似文献