The Kitasato archives of experimental medicine最新文献

{"title":"Drug resistance plasmids of Actinobacillus (Haemophilus) pleuropneumoniae serotype 2 strains isolated from swine.","authors":"K Kawahara,&nbsp;H Kawase,&nbsp;T Nakai,&nbsp;K Kume,&nbsp;H Danbara","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Drug resistance plasmids were detected in two drug resistant strains of Actinobacillus (Haemophilus) pleuropneumoniae serotype 2 isolated in Japan. One strain, Hpn25, was resistant to ampicillin, kanamycin, streptomycin and sulfonamides, and harbored two plasmids with a molecular size of 3.7 and 4.1 kilobases (kb). The other strain, Hpn18, which was resistant to streptomycin, tetracycline, and chloramphenicol, harbored three plasmids with a molecular size of 2.2, 12, and 35 kb. The resistance of Hpn 25 to streptomycin and sulfonamides is mediated by a 4.1 kb plasmid and that of Hpn 18 to streptomycin and chloramphenicol by one or more of the 2.2, 12, and 35 kb plasmids.</p>","PeriodicalId":76691,"journal":{"name":"The Kitasato archives of experimental medicine","volume":"63 2-3","pages":"131-6"},"PeriodicalIF":0.0,"publicationDate":"1990-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13252088","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Dr. Toju Hata and Dr. Satoshi Omura received the Japan Academy Award.","authors":"H Tanaka","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76691,"journal":{"name":"The Kitasato archives of experimental medicine","volume":"63 2-3","pages":"65-76"},"PeriodicalIF":0.0,"publicationDate":"1990-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13252090","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The immunobiological properties expressed in vitro and in vivo of Salmonella enteritidis-induced murine T cell lines.","authors":"T Sasahara","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Splenic T lymphocytes from two strains of mice, BALB/c and B10.BR, infected with an attenuated strain of Salmonella enteritidis were cloned by the double-layer soft agar technique in the presence of interleukin 2 (IL 2), formalin-killed S. enteritidis (FKS) and syngeneic feeder cells. One Salmonella-reactive T cell line was established from each strain of mice. Both T cell lines bore Thy-1+, Lyt-1+ and L3T4+ surface markers as demonstrated by cytofluorography. Biological properties of the T cell lines were studied with respect to their ability to proliferate and produce lymphokines such as IL 2 and gamma-interferon (IFN-gamma) in response to Salmonella antigens, and to transfer adoptively protection against infection and delayed-type hypersensitivity (DTH). As the result of the present study, the T cell lines were proliferated specifically against several Salmonella and other bacteria, which belong to species of Enterobacteriaceae. Their proliferation required the presence of the specific antigen(s) and the compatibility in the I-A region of the H-2 complex between the T cell lines and feeder cells. The T cell lines could be proliferated with resultant production of IL 2 and IFN-gamma by in vitro culture in the presence of syngeneic feeder cells and Salmonella antigens. The protective activity assessed by the number of recoverable bacteria in spleens and livers after challenge with virulent S. enteritidis and DTH reactions to Salmonella antigen were exhibited by the T cell lines when transferred adoptively to naive syngeneic mice. These results suggested that different biological functions of cell-mediated immunity to Salmonella could be mediated by a single phenotype of T cell population.</p>","PeriodicalId":76691,"journal":{"name":"The Kitasato archives of experimental medicine","volume":"63 2-3","pages":"107-18"},"PeriodicalIF":0.0,"publicationDate":"1990-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13123316","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Molecular biology of type A endogenous retrovirus.","authors":"M Ono","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Intracisternal A particles (IAPs) are retrovirus-like structures consistently observable in a variety of mouse tumor cells such as myeloma and hybridoma and in early embryonic cells derived from rodents but nothing is known of their infectivity. Mouse IAPs contain a gag-like protein, a reverse transcriptase and a polyadenylated RNA molecule (IAP RNA). DNA sequences complementary to IAP RNA (IAP genome) are interspersedly present in rodent such as mice, rats, Chinese hamsters and Syrian hamsters at several hundred to a thousand copies per haploid genome. Molecularly cloned IAP genomes from two species Mus and Syrian hamster were 6 to 8 kb in length with LTRs of about 0.4 kb long. The nucleotide sequence of the Syrian hamster IAP genome, H18, predicted a typical LTR-gag-prt-pol-env-LTR structure, although many stop codons were present in the region corresponding to env. The comparison of the deduced amino acid sequences of the pol region showed IAP (type A), mouse mammary tumor virus (MMTV) (type B), and squirrel monkey retrovirus (SMRV) (type D) genomes to be closely related. By using a DNA fragment encoding the pol region of the Syrian hamster IAP genome, human endogenous retroviruses termed HERV-K, were cloned from a fetal human liver gene library. Typical HERV-K genome was 9.5 kb in length having LTRs of about 1.0 kb. The HERV-K provirus could encode gag (666 codons), prt (334 codons), pol (937 codons), and env (618 codons) genes. HERV-K was shown to be closely related to types A, B and D retroviruses. The HERV-K genomes are present at about 50 copies per haploid human genome. In several human tumor cell lines, the HERV-K genome was expressed as 8.8 kb poly(A)+ RNA which appeared to be a full-size transcript of this genome. In the human breast cancer cell line T47D, stimulation of HERV-K genome expression was observed following female steroids treatment. In a detailed investigation on the organization of HERV-K proviruses in human genome, we found repetitive sequences homologous to the LTR region of the HERV-K genome. They were about 630 bp in length with an A rich tail at 3' end and found to be a SINE type nonviral retroposon. These elements were present at 4,000 to 5,000 copies per haploid human genome.</p>","PeriodicalId":76691,"journal":{"name":"The Kitasato archives of experimental medicine","volume":"63 2-3","pages":"77-90"},"PeriodicalIF":0.0,"publicationDate":"1990-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12874515","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"[The haptoglobin-streptococcus relationship].","authors":"T Nagai","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>In many experiments beginning in 1977 Prof. O. Prokop and Prof. W. Köhler discovered that the human haptoglobins are able to agglutinate group G-streptococci, but the reaction depends on the haptoglobin type. Haptoglobins of the types Hp 2-2 and Hp 2-1 are complete agglutinins and haptoglobin of the Hp 1-1 type is incomplete (\"blocking\") antibody. Later it was found that streptococci with the T4--antigen (from Lancefield types A, C and G) are suitable for the test.</p>","PeriodicalId":76691,"journal":{"name":"The Kitasato archives of experimental medicine","volume":"63 1","pages":"7-10"},"PeriodicalIF":0.0,"publicationDate":"1990-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13424551","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"A long-term surveillance of occupational health hazards faced by cadmium workers.","authors":"Y Shibuya","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The decrease or damage of renal tubular functions by cadmium (Cd) exposure is designated as the critical effect on human body. When the Cd workers suffer from tubular damage, it is matter of concern whether the damage is reversible or irreversible. In this study, chronic influences of long-term exposure to Cd dust or fumes in the working environment were clarified. Besides the survey on Cd contents in work environment and production amounts of Cd pigments in the factory, the changes of Cd concentration in blood and urine, beta 2-microglobulin (beta 2MG) in serum and urine, C beta 2-MG/Ccr, the rate of tubular reabsorption of phosphorus (% TRP) and other laboratory examinations in 7 Cd pigment workers were observed for the past 15 years. In almost workers, the changes of Cd concentrations in blood and urine, beta 2MG in urine, and C beta 2MG/Ccr basically paralleled those of Cd concentrations in working environment. In some workers the fluctuations of beta 2MG in urine, C beta 2MG/Ccr and %TRP did not paralleled those of environmental Cd concentration and they were very variable. From the results obtained, it is stressed that the long-term follow-up studies on environmental Cd concentrations and analysis of biological indicators are necessary to determine the degree of the renal tubular dysfunction by Cd.</p>","PeriodicalId":76691,"journal":{"name":"The Kitasato archives of experimental medicine","volume":"63 1","pages":"37-48"},"PeriodicalIF":0.0,"publicationDate":"1990-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13424548","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Uptake and distribution of chromium in isolated rat hepatocytes and its relation to cellular injury.","authors":"S Ueno,&nbsp;N Susa,&nbsp;Y Furukawa","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>In order to study the difference of uptake and distribution between hexavalent (Cr6+) and trivalent (Cr3+) chromium in isolated rat hepatocytes, the cells were incubated with Cr6+ or Cr3+ (1 mM Cr) at 37 degrees C for up to 60 min. Leakage of lactate dehydrogenase from the hepatocytes into the suspension medium as an indicator of cellular injury was facilitated by Cr6+ (K2Cr2O7) at 60 min of incubation, whereas Cr3+ [Cr(NO3)3] had no effect. After 60 min of incubation with Cr6+, about 33% of the added Cr was found in the hepatocytes, whereas incubation with Cr3+ resulted in transfer of about 66% of the added Cr to the cells. After 20 and 40 min of incubation with Cr6+, about 39% of cellular Cr was found in the cytosolic fraction of hepatocytes, followed by a reduction to about 35% after 60 min of incubation. However, Cr detected in the cytosolic fraction of hepatocytes incubated with Cr3+ was about 1% of cellular Cr. Cr-binding substances in the cytosolic fraction of hepatocytes incubated with Cr6+ were eluted with two Cr peaks by Sephadex G-200 chromatography. These Cr-binding substances in the low-molecular-weight fractions were separable into at least two substances by thin-layer chromatography. These results suggest that Cr6+ readily passes through the cell membrane and combines with substances already present in the cytosolic fraction of hepatocytes, unlike metallothionein induced by cadmium, followed by detoxification. Consequently, cellular injury might be induced by Cr6+ which could not combine with LMCr in the cytosolic space of the hepatocytes.</p>","PeriodicalId":76691,"journal":{"name":"The Kitasato archives of experimental medicine","volume":"63 1","pages":"49-57"},"PeriodicalIF":0.0,"publicationDate":"1990-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13424549","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Staphylococcal food poisonings in Tokyo, with special reference to the coagulase types of the isolates.","authors":"H Ushioda,&nbsp;A Suzuki","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Staphylococcus aureus strains isolated from the 391 confirmed cases of staphylococcal food poisonings in Tokyo, in the period 1967-1986, were studied for their coagulase types. Consequently, it was found that all the isolates could be classified into the coagulase types II, III, VI and VII. Namely, the isolates from 54 (13.8%) of 391 outbreaks were typed as type II, 72 (18.4%) as type III, 38 (9.7%) as type VI, and 227 (58.1%) as type VII, respectively. Throughout the investigation, it was found that the outbreaks of staphylococcal food poisonings due to coagulase type VII organisms were remarkably increased since 1975.</p>","PeriodicalId":76691,"journal":{"name":"The Kitasato archives of experimental medicine","volume":"63 1","pages":"59-64"},"PeriodicalIF":0.0,"publicationDate":"1990-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13424550","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Differentiation of a human B cell hybridoma with interleukin-2 receptor.","authors":"N Ikewaki","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>A 6-thioguanine-neo-resistant clone, Raji 6-TGR-neoR was fused with pokeweed mitogen-stimulated B cells (PWM-B cells) obtained from a normal healthy donor, and selected by a new selection medium (HAT-neo). Two hybrid clones, HYNI-1 and HYNI-2, were established. These clones expressed surface IgG and HLA class II antigens derived from PWM-B cells, and they had about 20 more chromosomes than Raji 6-TGR-neoR. More significantly, one clone, HYNI-2, expressed interleukin-2 receptor on the cell surface, and generated IgG when stimulated with recombinant interleukin-2. These findings indicate that the HYNI-2 is a good model for studying human B cell differentiation.</p>","PeriodicalId":76691,"journal":{"name":"The Kitasato archives of experimental medicine","volume":"63 1","pages":"31-6"},"PeriodicalIF":0.0,"publicationDate":"1990-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13424547","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Advances in research on DT-diaphorase--catalytic properties, regulation of activity and significance in the detoxication of foreign compounds.","authors":"S Horie","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>DT-diaphorase [NAD(P)H dehydrogenase (quinone), EC 1.6.99.2] is a flavoprotein enzyme widely distributed in the cytosolic fractions of various animal tissues. It is also called menadione reductase or NAD(P)H-quinone reductase and catalyzes NAD(P)H-dependent 1-, 2- or 4-electron reduction of certain redox dyes, aromatic nitro compounds, aromatic C-nitroso compounds and probably azo-dyes, as well as menadione (vitamin K3) and other quinones. Dicumarol exerts characteristic inhibition on DT-diaphorase, whereas serum albumin and certain non-ionic detergents exert activation. Excessive concentrations of many of the electron acceptors inhibit the activity of this enzyme. The physiological significance of DT-diaphorase is still obscure because the physiological vitamins (K1 and K2) and coenzyme Q10 are difficult to reduce with this enzyme. Results of recent studies suggest that DT-diaphorase prevents formation of active oxygen species. Activities in liver and other tissues are known to be enhanced by administration of chemicals including certain carcinogens such as 3-methylcholanthrene (3-MC), anti-oxidants such as 3-tert-butyl-4-hydroxyanisole (BHA), and other compounds. Both basal and induced activities vary considerably with tissue, sex, strain and species of animals. The strain variations in activities in rat and mouse liver are known to be inherited, and the trait of hereditary transmission can be adequately explained by postulating two loci of genes or gene clusters regulating the activity. Resistance of animals to various toxic or carcinogenic substances may be promoted by BHA administration and depressed by dicumarol administration. Thus, attention has been focused on the role played by DT-diaphorase in the detoxication of foreign compounds. Knowledge on strain variations in basal and induced activities of tissue DT-diaphorase is of potential value when choosing a rat or mouse strain suitable for studying the toxic effects of drugs, especially drugs expected to be detoxified by reductive metabolism. With future progress in research on DT-diaphorase, this enzyme might be applied to prophylactic and therapeutic medicine.</p>","PeriodicalId":76691,"journal":{"name":"The Kitasato archives of experimental medicine","volume":"63 1","pages":"11-30"},"PeriodicalIF":0.0,"publicationDate":"1990-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13280042","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}