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1.
Neuroscience ; 120(1): 283-9, 2003.
Article in English | MEDLINE | ID: mdl-12849760

ABSTRACT

In order to investigate neural mechanisms by which the prefrontal cortex adaptively modifies its activities based on past experience, we examined whether or not sensory cortical projections to the medial prefrontal cortex support long-term potentiation (LTP) in rats. Monosynaptic projections from the secondary visual cortex, mediomedial area (V2MM) to the infralimbic cortex were confirmed by orthodromic as well as antidromic activation of single units. High-frequency stimulation (50 Hz, 2 s) induced LTP (approximately 45% increase over the baseline) in the V2MM projection to the infralimbic cortex. LTP induction in this pathway was completely blocked by an injection (i.p.) of CPP, an N-methyl-D-aspartate receptor antagonist. LTP was also induced in the ventral hippocampal projection to the infralimbic cortex by the same high-frequency stimulation. The present results suggest that modification of synaptic weights of afferent sensory cortical projections is one mechanism underlying learning-induced changes in prefrontal cortical neural activities.


Subject(s)
Long-Term Potentiation/physiology , Prefrontal Cortex/physiology , Visual Cortex/physiology , Visual Pathways/physiology , Animals , Male , Rats , Rats, Sprague-Dawley
2.
Mol Gen Genet ; 261(2): 323-36, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10102368

ABSTRACT

We have used RT-PCR and GFP-mediated fluorescence to analyse the regulation of PrfA-dependent virulence genes of Listeria monocytogenes during proliferation in mammalian host cells. Our data show that most of the PrfA-regulated virulence genes are more efficiently expressed, as measured by transcript levels, when L. monocytogenes is grown in macrophages and macrophage-like cells rather than in epithelial cells, hepatocytes or endothelial cells. The promoters for hly and plcA are predominantly activated within the phagosomal compartment, while those for actA and inlC are predominantly activated in the host cell cytosol. Expression of actA and plcB precedes that of inlC after infection of epithelial cells and macrophages. Little transcription of inlA or inlB is observed in epithelial cells and there is only slightly more in macrophages. In both cell types the level of transcription of the inlAB operon is lower than is seen under extracellular growth conditions in rich media, which is compatible with the assumption that InlA and InlB are not required during intracellular growth of the bacteria. Activation of the PrfA-independent iap promoter is also low during intracellular growth, although the gene product (p60) is required for cell viability. The levels of the PrfA-dependent virulence gene transcripts do not correlate with the amount of prfA transcript present, which is low under all intracellular conditions analysed, suggesting that the prfA transcript is either highly unstable in bacteria that are growing intracellularly, or that the small amount of PrfA produced is highly activated by additional component(s).


Subject(s)
Bacterial Proteins/metabolism , Gene Expression Regulation, Bacterial , Genes, Bacterial , Listeria monocytogenes/genetics , Trans-Activators/metabolism , Animals , Caco-2 Cells , Cell Compartmentation , Cell Line , Cells, Cultured , Fluorescence , Green Fluorescent Proteins , Humans , Listeria monocytogenes/growth & development , Listeria monocytogenes/pathogenicity , Luminescent Proteins/genetics , Macrophages/cytology , Mammals , Mice , Mice, Inbred BALB C , Peptide Termination Factors , Plasmids , Promoter Regions, Genetic , Reverse Transcriptase Polymerase Chain Reaction , Transcription, Genetic , Virulence
3.
Mol Microbiol ; 21(4): 823-37, 1996 Aug.
Article in English | MEDLINE | ID: mdl-8878044

ABSTRACT

A mutant of Listeria monocytogenes EGD was constructed that carries an extended deletion removing the entire PrfA-regulated gene cluster from plcA to plcB and a second deletion inactivating the inlA gene. Upon supplementation of this mutant with multiple gene copies of prfA, a protein of 30 kDa was detected in the supernatant of the mutant strain. The gene encoding this protein was obtained by direct and inverse polymerase chain reaction using oligonucleotide primers that were deduced from partial amino acid sequences of the purified 30 kDa protein. The amino acid sequence of the gene product revealed a protein of 297 amino acids that carried eight repeat units with high homology to those of the two known internalin proteins A and B. This secretory protein, termed internalin C, is much smaller than InlA or InlB and its complete sequence is related to the two known internalins. The gene InlC is transcribed into a monocistronic mRNA from a single promoter which shows a typical consensus sequence for PrfA-binding at the position -40. In contrast to the transcription of the InlAB operon, which is downregulated after shift of an L. monocytogenes EGD culture from brain-heart infusion into minimum essential medium (MEM), transcription of inlC is induced in MEM like most of the other known PrfA-regulated virulence genes. In addition, InlC is strongly transcribed in the cytoplasm of phagocytic J774 cells whereas inlA is poorly transcribed under these conditions, suggesting that internalin C may play a role in a late stage of L. monocytogenes infection rather than in the uptake of L. monocytogenes by non-professional phagocytic cells. An InlC deletion mutant shows reduced virulence when tested in an intravenous mouse model, but intracellular replication of the mutant in Caco-2 and J774 cells appears to be comparable with that of the wild-type strain.


Subject(s)
Bacterial Proteins/genetics , Bacterial Proteins/physiology , Genes, Bacterial/genetics , Listeria monocytogenes/genetics , Trans-Activators/physiology , Amino Acid Sequence , Animals , Bacterial Proteins/chemistry , Bacterial Proteins/isolation & purification , Base Sequence , Caco-2 Cells , Cloning, Molecular , Culture Media , Gene Expression Regulation, Bacterial/physiology , Humans , Listeria monocytogenes/growth & development , Listeria monocytogenes/pathogenicity , Mice , Mice, Inbred C57BL , Molecular Sequence Data , Molecular Weight , Peptide Termination Factors , RNA, Bacterial/analysis , RNA, Messenger/analysis , Sequence Analysis , Sequence Homology, Amino Acid , Species Specificity , Trans-Activators/genetics , Transcription, Genetic , Virulence
4.
Planta Med ; 62(2): 183-4, 1996 Apr.
Article in English | MEDLINE | ID: mdl-17252435

ABSTRACT

2'-Hydroxycinnamaldehyde, which inhibits farnesyl-protein transferase (FPTase), has been isolated from the stem bark of Cinnamomum cassia Blume. The biologically active agent in the extract has been purified by silica column chromatography and HPLC. The structure of the isolated compound was elucidated on the basis of 500 MHz NMR experiments.

5.
Biol Trace Elem Res ; 43-45: 229-37, 1994.
Article in English | MEDLINE | ID: mdl-7710832

ABSTRACT

For a case study of environmental pollution, radiochemical neutron activation analysis (RNAA) was applied to the crucian and rice collected along the Han River. The crucian was analyzed for three times in 1973, 1987, and 1990. Sixteen trace elements (Hg, Cd, As, Br, Cu, Na, K, Se, Cr, Hf, Rb, Fe, Zn, Co, La, and Cs) were determined by RNAA using distillation and diethyldithiocarbamate extraction methods. Contents of Na, K, Se, Hf, Fe, Zn, and Co were almost constant regardless of the sampling place and year. The contents of the other elements showed increasing trends down river, especially in the first investigation. At the lower part of the river, the contents showed decreasing trends with the time of sampling, especially during the first two investigations. These trends were typical for Hg and Cd. Rice was analyzed by the same method for 12 elements, and the results showed no regional trends, but have decreased after 1973.


Subject(s)
Fishes/metabolism , Oryza/chemistry , Trace Elements/analysis , Water Pollutants, Chemical/analysis , Animals , Korea , Neutron Activation Analysis
6.
8.
J Natl Med Assoc ; 61(4): 362-4, 1969 Jul.
Article in English | MEDLINE | ID: mdl-5796412
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