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Biomedical subjects

J R Smith

Publications and source records attributed to J R Smith.

At least 307 records · Page 17Linked to original sources

A potent DNA synthesis inhibitor expressed by the immortal cell line SUSM-1.

We have previously reported the production of DNA synthesis inhibitor proteins by both quiescent and senescent human diploid fibroblasts. Young, proliferating fibroblasts do not produce such inhibitors, but are capable of responding to either the quiescent or senescent cell DNA synthesis inhibitors. Recently, we have analyzed the immortal cell line SUSM-1 (derived from normal liver fibroblasts following exposure to carcinogen) for inhibitory activity. We have found that SUSM-1 cells produce a factor capable of inhibiting DNA synthesis in young fibroblasts. Crude extracts prepared from SUSM-1 cells inhibit DNA synthesis in a dose-dependent manner at concentrations 10-fold lower than those of either senescent or quiescent fibroblast cell extracts. SUSM-1 cells are incapable of responding to the inhibitor they produce, as are three other immortal human cell lines tested. One immortal cell line, HeLa, does respond to the SUSM-1 inhibitor, though to a lesser degree than observed with normal young fibroblasts. One hypothesis is that the DNA synthesis inhibitor protein(s) of senescent cells plays a role in determining the finite in vitro life span of normal cells. The results reported here suggest that SUSM-1 cells may have escaped senescence through loss of a receptor or cofactor for the inhibitor protein(s).

Cell Extracts↗

A data compression algorithm for the electroencephalogram.

This paper describes a data compression algorithm for the EEG using a local error measure. The algorithm discards input signal samples provided they can be reconstructed from the stored samples with an error smaller than a given threshold, and according to simple reconstruction functions (the hold, the ramp, and the cosine). An equivalent (in terms of storage) sampling rate of 44 Hz is achieved without noticeable degradation of the signal quality for visual analysis. The method can be easily implemented for real time multichannel data compression/reconstruction.

Algorithms↗

Electrical stimulation of the human hippocampus produces verbal intrusions during memory testing.

Verbal memory testing was conducted during electrical stimulation of the human hippocampus in 12 epilepsy surgery candidates with unilateral temporal lobe seizure onset. Performance was assessed during baseline, left hippocampal stimulation and right hippocampal stimulation. Verbal intrusion errors were greater during electrical stimulation of the hippocampus contralateral to the seizure focus. These findings suggest that verbal intrusions are related to memory deficits, and that patients with cerebral disease who intrude words from an earlier portion of a learning test are likely to have bilateral cerebral dysfunction.

Adult↗

An extended HLA-D region haplotype associated with celiac disease.

Celiac disease has one of the strongest associations with HLA (human leukocyte antigen) class II markers of the known HLA-linked diseases. This association is primarily with the class II serologic specificities HLA-DR3 and -DQw2. We previously described a restriction fragment length polymorphism (RFLP) characterized by the presence of a 4.0-kilobase Rsa I fragment derived from an HLA class II beta-chain gene, which distinguishes the class II HLA haplotype of celiac disease patients from those of many serologically matched controls. We now report the isolation of this beta-chain gene from a bacteriophage genomic library constructed from the DNA of a celiac disease patient. Based on restriction mapping and differential hybridization with class II cDNA and oligonucleotide probes, this gene was identified as one encoding an HLA-DP beta chain. This celiac disease-associated HLA-DP beta-chain gene was flanked by HLA-DP alpha-chain genes and, therefore, was probably in its normal chromosomal location. The HLA-DP alpha-chain genes of celiac disease patients also were studied by RFLP analysis; 84% of HLA-DR3, -DQw2 patients had a 16-kb Xba I fragment that was present in only 36% of HLA-DR3, -DQw2 controls. Moreover, 79% of these patients had both alpha- and beta-chain polymorphisms in contrast to 27% of controls. Thus, celiac disease is associated with a subset of HLA-DR3, -DQw2 haplotypes characterized by HLA-DP alpha- and beta-chain gene RFLPs. Within the celiac-disease patient population, the joint segregation of these HLA-DP genes with those encoding the serologic specificities HLA-DR3 and -DQw2 indicates: (i) that the class II HLA haplotype associated with celiac disease is extended throughout the entire HLA-D region, and (ii) that celiac-disease susceptibility genes may reside as far centromeric on this haplotype as the HLA-DP subregion.

B-Lymphocytes↗

Genetic analysis of indefinite division in human cells: identification of four complementation groups.

Hybrids obtained following fusion of normal human diploid fibroblasts with different immortal human cell lines exhibited limited division potential. This led to the conclusion that the phenotype of cellular senescence is dominant and that immortal cells arise as a result of recessive changes in the growth control mechanisms of the normal cell. We have exploited the fact that immortality is recessive and, by fusing immortal human cell lines with each other, assigned 21 cell lines to at least four complementation groups for indefinite division. A wide variety of cell lines was included in the study to determine what parameters, if any, would affect complementation group assignment. The results indicate that cell type, embryonal layer of origin, and type of tumor do not affect group assignment. There does not appear to be any correlation between expression of an activated oncogene and group assignment. However, all of the immortal simian virus 40-transformed cell lines studied (with the exception of one xerodermapigmentosum fibroblast-derived line) assign to the same group, indicating that this virus immortalizes various human cells by the same processes. The assignment of immortal human cells to distinct groups provides the basis for a focused approach to determine the genes important in normal growth regulation that have been modified in immortal cells.

Cell Division↗

Multiple genes encode nuclear factor 1-like proteins that bind to the promoter for 3-hydroxy-3-methylglutaryl-coenzyme A reductase.

DNA-binding proteins of the nuclear factor 1 (NF1) family recognize sequences containing TGG. Two of these proteins, termed reductase promoter factor (RPF) proteins A and B, bind to the promoter for hamster 3-hydroxy-3-methylglutaryl-coenzyme A reductase, a negatively regulated enzyme in cholesterol biosynthesis. In the current study, we determined the sequences of peptides derived from hamster RPF proteins A and B and used this information to isolate a cDNA, designated pNF1/Red1, that encodes RPF protein B. The peptide sequence of RPF protein A, the other reductase-related protein, suggests that it is the hamster equivalent of NF1/L, which was previously cloned from rat liver. We also isolated a hamster cDNA for an additional member of the NF1 family, designated NF1/X. Thus, the hamster genome contains at least three genes for NF1-like proteins. It is likely to contain a fourth gene, corresponding to NF1/CTF, which was previously cloned from the human. The NH2-terminal sequences of all four NF1-like proteins (NF1/Red1, NF1/L, NF1/X, and NF1/CTF), which are virtually identical, contain the DNA-binding domain that recognizes TGG. Functional diversity may arise from differences in the COOH-terminal sequences. We hypothesize that the COOH-terminal domain interacts with adjacent DNA-binding proteins, thereby stabilizing the binding of a particular NF1-like protein to a particular promoter. This protein-protein interaction confers specificity to a class of proteins whose DNA-recognition sequence is widespread in the genome. Sterols may repress transcription of the reductase gene by disrupting this protein-protein interaction.

Amino Acid Sequence↗

Relationship of limbic evoked potentials to recent memory performance.

The relationship between limbic evoked potentials (LEPs) and memory performance was investigated in eight patients with intractable epilepsy who were candidates for temporal lobectomy. No relationship between the presence or absence of unilateral LEP and memory deficits was present. However, in both patients with bilaterally poorly developed hippocampal LEPs, verbal and visual-spatial memory tasks were impaired. In one patient with well developed LEPs bilaterally, memory function was normal. These data suggest that LEPs may assist in the evaluation of memory function during the preoperative work-up for temporal lobectomy.

Epilepsy↗

Preserved crossmodal association following bilateral amygdalotomy in man.

The present study investigated the role of the amygdala in crossmodal association in man. Recent experimental evidence indicates amygdalectomized monkeys show deficits when required to identify, through vision, objects that have been previously examined by touch. We employed a delayed nonmatching to sample task pre- and postoperatively in a patient who underwent bilateral stereotaxic amygdalotomy for intractable aggressivity. Bilateral amygdalotomy did not impair our patient's ability to associate an object from one sensory modality to another, following a short delay. The results suggest that sensory association memory does not depend upon the amygdala in humans. Examination of the neuroanatomic structures affected by the differing surgical procedures in the two species revealed entorhinal and perirhinal cortices were damaged in amygdalectomized monkeys but not in the present case. Because entorhinal cortex is an important structure for the formation of new memory traces, it is possible that damage to the entorhinal and surrounding cortical regions, rather than damage to the amygdala itself, is responsible for the crossmodal association deficit in monkeys.

Adult↗

Cholinergic modulation of human limbic evoked potentials.

Limbic evoked potentials (LEPs) were recorded from the hippocampi of three epilepsy surgery patients with unilateral medial temporal lobe seizure onset. In each patient, stable large amplitude LEPs which displayed polarity inversion across successive levels of hippocampus were present unilaterally, but were absent or rudimentary in the hippocampus corresponding to the electrographically proven seizure onset. After administration of scopolamine, LEPs in the "normal" hippocampi were markedly altered with slowing of the individual components and increased trial to trial variability. In addition, two patients developed reliable, high amplitude, polarity inverting LEPs on the side of seizure onset which had either absent or rudimentary LEPs in the baseline state. The results suggest that LEPs are under cholinergic modulation.

Acetylcholine↗

Thrombotic thrombocytopenic purpura: treatment with plasmapheresis.

Twenty-one episodes of thrombotic thrombocytopenic purpura (TTP) were treated with plasmapheresis. Adjunctive agents included corticosteroids, aspirin, dipyridamole, and vincristine. There were 17 patients; 12 were female. The median age was 41 years. Most patients presented with neurologic symptoms. Thrombocytopenia was profound with a mean initial platelet count of 14,900/mm3. The mean hematocrit on presentation was 26.7% and the mean LDH 1300 IU/L. Eighteen episodes responded completely following plasmapheresis/plasma exchange (86%). Response was prompt, the initial rise in platelet count occurred after a mean of four exchanges, and complete response (a platelet count over 150,000/mm3) was obtained after a mean of nine exchanges. Four of the episodes treated were relapses that occurred in three patients. All responders are alive with a median duration of follow-up of 20 months. The three patients who failed to respond have died. This report extends recent observations that the addition of plasmapheresis/plasma exchange to the therapy of TTP has significantly improved the outlook for patients with this disorder.

Adrenal Cortex Hormones↗

Filter transient response to EEG waveforms.

The response of two types of linear filters to sinusoidal bursts was calculated to demonstrate how filters can distort EEG waveforms. Results show that the wider the filter bandwidth the less is the distortion, and for a given bandwidth, the higher the filter order the greater the distortion. The response of a linear phase filter was also calculated to demonstrate that this type of filter can also cause waveform distortion, although it is normally less than that caused by Butterworth, Tchebychev and elliptic filters.

Electroencephalography↗

Aflatoxin B1 activation to a plasmid mutagen by a chemical model of cytochrome P-450.

Aflatoxin B1 (AFB1) was oxidised by a chemical model of cytochrome P-450 and the products obtained analysed by reversed-phase hplc. The oxidation system employs a water-insoluble iron(III)porphyrin catalyst (tetraphenylporphinatoiron(III) chloride; FeTPPCl) and an oxygen donor, iodosylbenzene (PhIO). The two AFB1 products obtained from this reaction were derived by initial oxidation across the 8-9 double bond of AFB1 and subsequent breakdown of AFB1-8,9-epoxide, the compound postulated to be the ultimate carcinogenic and mutagenic derivative of AFB1. Oxidation of AFB1 by the porphyrin-catalysed system in the presence of calf-thymus DNA, resulted in the formation of AFB1-DNA adducts identical to those formed in vivo and in vitro after liver mono-oxygenase activation. The chemical model system was therefore used on a microscale to react AFB1 with plasmid pHR1800, a plasmid containing the genes for beta-lactamase (amp-r) and galactokinase (galK). AFB1-modified plasmid DNA was then transformed into E. coli AB1886 (uvrA-) and the effects of the AFB1-DNA adducts on plasmid survival and the ability of pHR1800-transformed bacteria to metabolise galactose, were then studied. The results showed an AFB1 dose-dependent decrease in plasmid survival and increase in the mutation frequency of the galK gene only when the complete oxidation system was used to generate the reactive AFB1 metabolite.

Aflatoxin B1↗

Differentiating tumours of the deep and superficial lobes of the parotid gland by computed tomographic sialography.

Parotid computed tomography (CT) combined with sialography is an established method of determining intrinsic from extrinsic tumours in and around the parotid gland. However, differentiation of deep from superficial lobe tumours lacks reliability. Various anatomical landmarks including Stensen's duct, the retromandibular vein, the styloid process, the posterior belly of the digastric muscle and more recently an arc 8.5 mm from the posterior border of the mandible have been used to predict the course of the facial nerve and hence divide the parotid into its deep and superficial portions. Our recent experience of CT in 17 cases of intrinsic parotid tumours and the results of surgery have been reviewed in an attempt to assess the reliability of these various landmarks. In 14 out of the 17 cases (82%) the relationship of the Stensen's duct to the tumour was well shown, and correct differentiation of deep from superficial lobe tumours could be made. We conclude that the relationship of the tumour to the Stensen's duct is most accurate in differentiating tumours of the deep and superficial lobes of the parotid.

Adenolymphoma↗