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Biomedical subjects

F H Kasten

Publications and source records attributed to F H Kasten.

At least 19 recordsLinked to original sources

Paul Ehrlich: pathfinder in cell biology. 1. Chronicle of his life and accomplishments in immunology, cancer research, and chemotherapy.

The paper reviews the life of Paul Ehrlich and his biomedical accomplishments in immunology, cancer research, and chemotherapy. Ehrlich achieved renown as an organic chemist, histologist, hematologist, immunologist, and pharmacologist. He disliked the formality of school but managed to excel in Latin and mathematics. His role model was an older cousin, Carl Weigert, who became a lifelong friend. Ehrlich studied medicine at Breslau, Strasbourg, Freiburg, and Leipzig, coming under the influence of Wilhelm Waldeyer, Julius Cohnheim, Rudolf Heidenhein, and Ferdinand Cohn. As a medical student, Ehrlich was captivated by structural organic chemistry and dyes. When he was 23, his first paper was published on selective staining. His doctoral thesis, "Contribution to the Theory and Practice of Histological Staining" contained most of the germinal ideas that would guide his future career. Most of his early work was centered in Berlin at Charite Hospital, where he did pioneering studies on blood and intravital staining, and at Robert Koch's Institute for Infectious Diseases, where he undertook important investigations in immunology. Ehrlich became an authority on antitoxin standardization and developed the "side-chain theory" of antibody formation for which he was later awarded the Nobel Prize. He became director of an Institute for Experimental Therapy in Frankfurt where he continued research in immunology and carried out routine serum testing. He developed new lines of investigation in cancer research and originated the field of chemotherapy. Using principles developed in his early work with dyes, he successfully treated certain experimental trypanosomal infections with azo dyes. His crowning accomplishment was discovering that the compound Salvarsan could control human syphilis. Ehrlich's legacy in immunology and chemotherapy is discussed and an intimate portrait is drawn of Ehrlich the person.

Allergy and Immunology↗

Radiopaque acrylic resins containing miscible heavy-metal compounds.

Radiopacity is needed in order to facilitate diagnosis of polymeric appliances, which may be dislodged and become impacted in the upper respiratory or digestive tracts. In order for a stable, optically transparent, radiopaque material to be provided, heavy-metal compounds were investigated which we had previously shown to form homogeneous structures with methyl methacrylate-based systems. It was found that, when present in PMMA at 11 to 14%, several compounds of either bismuth or uranium or 35% of an organo-zirconium compound impart radiopacity equivalent to that of aluminum. A low level of cytotoxicity and lack of mutagenicity indicated that a high level of biocompatibility can be expected. Processing characteristics are somewhat altered, but formulations satisfactory for use in various dental devices were found.

Acrylic Resins↗

Biocompatibility testing of an experimental fluoride releasing resin using human gingival epithelial cells in vitro.

Cell culture is a valuable method of evaluating the biocompatibility of new dental materials. The purpose of this study was to compare the in vitro biocompatibility of an experimental fluoride composite resin with fluoride and non-fluoride-releasing materials currently available. The dental materials tested were: MQ Silicate (silicate cement), KETAC-CEM and FUJI (type II glass ionomer cements), VISIO DISPERS (a light-cured, nonfluoridated, microfilled composite resin), and FR-17 (an experimental fluoride-releasing composite resin). The Smulow-Glickman (S-G) human gingival epithelial cell line, which exhibits semidifferentiated characteristics, was used in the study as a test system. Biocompatibility was quantified by counting the viable cells per unit area remaining after 24 and 48 h at two radial distances from cured specimens immersed in the cell culture medium. The test materials were observed to be most toxic to cells nearest the materials. A Time-Distance Cytotoxicity Index (TDCI) was calculated to relate the percentage of dead cells to viable cells at each diffusion distance for each exposure time compared to a nontoxic control. The relative toxicity ranking of the materials tested based on the TDCI was VISIO DISPERS (91%), FUJI (82%), FR-17 (30%), MQ Silicate (23%), and KETAC-CEM (10%), which exhibited the least toxicity. The cytotoxicity of the experimental resin FR-17 was within the range of cytotoxicity of currently accepted restorative materials.

Cell Survival↗

Polarized light microscopy in the study of the molecular structure of collagen and reticulin.

Although collagen structure has been studied by polarized light microscopy since the early 19th century and continued since, modern studies and reviews failed to correlate the conclusions based on data obtained by the techniques with those of polarized light microscopy. Collagen I is intensely positively birefringent in respect to length of the fibres; the positive intrinsic birefringence indicates a quasi-crystalline alignment parallel to the fibre and molecule axis of the amino acid residues of the polypeptide chains. This would not have been compatible with a helical structure but has been achieved by similar tilt angles and opposite directions of the coiling and supercoiling. Birefringence characteristics of collagen are also affected by chemical treatments, extractions and staining procedures. Attachment of chemical groups to the anionic charges present on the surface of collagen molecules results in increased positive birefringence in the case of bipolar molecules attached to two or more anionic residues. Unipolar attachment to the same groups, or to the cationic groups of the associated proteoglycans, as well as sulfation or acetylation of hydroxyls of the protein and/or the carbohydrate, reduced or reversed the sign of birefringence. Increased birefringence caused by stretching cannot be due to intramolecular events and is caused by intermolecular changes. The same applies to changes in collagen during aging. Reticulin is a group of different substances which mostly contain collagen III. The pliability and deformability of this collagen is related to its weakly negative birefringence due to large side chains and presence of different and greater amounts of interstitial proteoglycans and other molecules. The so-called reticulin of healing wounds differs in its constitution from other reticulins but is also rich in intermolecular carbohydrate components.

Birefringence↗

Erythropoietin production in a primary culture of human renal carcinoma cells maintained in nude mice.

The present studies report erythropoietin (Ep) production in primary cultures of a human renal carcinoma from a patient with erythrocytosis that has been serially transplanted to BALB/c nude mice. The levels of erythropoietin in the culture media were estimated using the exhypoxic polycythemic mouse assay (EHPCMA), fetal mouse liver erythroid colony-forming technique (FMLC), and a radioimmunoassay (RIA). The spent culture media of the exponentially growing cells contained less than 10 mU/ml of Ep measured by RIA. However, after the cells became confluent, Ep levels (RIA) in the spent media showed a marked increase to approximately 300 mU/ml. Ep levels estimated using the FMLC and EHPCMA were approximately 2/3 and 1/10, respectively, of those measured by RIA. Rabbit antiserum to highly purified human urinary Ep (70,400 U/mg protein) was utilized for immunocytochemical (peroxidase-antiperoxidase method) localization of Ep in the cultured cells. Very few of the cells in exponential growth exhibited Ep-like immunoreactivity, whereas intense Ep-like immunoreactivity was observed in the cytoplasm of the cells maintained in culture for a prolonged period after reaching confluency. The most intense staining was observed in some of the cells forming domes. The domes developed after the cells reached confluency, and their numbers increased with increasing time in confluent culture, in parallel with the increase in Ep levels in the spent media. This primary cell culture system of a renal cell carcinoma maintained in nude mice, which produces immunologically and biologically active Ep, may provide a useful model for studies of the mechanism of Ep production.

Animals↗

[Golgi apparatus and T-tubules in cultured myocytes of rat hearts].

The cytochemical-ultrastructural study of rat ventricular cells grown in tissue culture supported the findings of Kasten (1971) on the existence of a special type of Golgi apparatus around the base of the nucleus of the myocardial cell. TPPase and ATPase activity are also found at the subsarcolemmal cisterns and the lateral vesicles of the sarcoplasmic reticulum. Therefore, well developed triads and diads are visible. These structures, however, require the existence of T-tubules in the cultured neonatal myocardial cells. Up to now the presence of T-tubules in early cultures of rat myocytes was still controversy. The demonstration of the T-tubules completes our knowledge of cultured cardiac myocytes and should be taken into consideration in further biochemical and physiological studies with this in vitro model.

Animals↗

A model culture system with human gingival fibroblasts for evaluating the cytotoxicity of dental materials.

A model experimental culture system and protocol are described to screen polymerized dental materials for diffusible toxic products. The system employs cultures of human gingival fibroblasts grown in plates containing immobilized samples of polymerized resins. Comparative cytoxicity is evaluated by counting viable cells with the aid of phase optics at several time periods up to 48 h. To achieve adequate statistical sampling, multiple counts are made in four different zones at 90 degrees angles from each sample and at three distances from the centers of samples. The most significant data were generated during a 24 to 48 h test period in climate. This cytotoxicity test measured cell death as a function of time of exposure and distance from the sample (24 h, 0 to 3 mm; 48 h, 3 to 6 mm) and permitted a calculation of the relative cytoxicity for each material, which is termed the viability index (VI). This can be expressed as a percentage related to the control, which is called the time-distance cytotoxicity index (TDCI). This method is simple to carry out because it used basic laboratory equipment, is rapid, and has a sound scientific basis. It focuses on times and distances when or where, or both, the greatest cellular changes are taking place. Some data illustrated are based on the screening of eight different restorative resins. The literature of cell culture testing of dental materials is reviewed. It is concluded that biotoxicity studies ideally should employ diploid human target cells from the oral cavity because the cells retain specialized features. Secondary cultures or strains of human diploid gingival fibroblasts, which are relatively easy to obtain and maintain, are recommended as cells of choice for screening dental restorative materials in vitro.

Adult↗

Hormonal secretion of cultured rat ovarian follicles isolated at various hours of proestrus.

Rat ovarian follicles were isolated at nine different times during proestrus and cultured for 3 d. During the period of cultivation, estrogen and progestagen secretion was measured. Other follicles were dissected out at the same time periods and analyzed directly for these hormones. The most intense hormone release was observed during the first 24 h in culture. The concentration of steroids secreted in vitro by follicles previously collected on the morning of proestrus was relatively low. The secreted estrogen concentration increased gradually from follicles previously isolated at later times during proestrus, with a maximum at 1800. The peak secretion of progestagens in culture was from follicles isolated at 2000. There was a marked decrease in secretion of both hormones from follicles isolated past their optimal times. The same secretion pattern of estrogens and progestagens was shown by follicles in vitro at 24 h as with similar follicles in vivo, according to their time of isolation. From these results it is evident that the normal rhythm of steroid secretion, predetermined at the time of follicle excision, was maintained during 24 h in organ culture. After a longer period in culture, the dynamics of hormone synthesis became altered, although follicles appeared morphologically normal up to 48 h.

Adult↗

Morphometric study of endomyocardium and epimyocardium of the left ventricle in adult dogs.

Quantitative light- and electron-microscopic data are reported for the endomyocardium and epimyocardium of the left ventricle in adult dogs. The endomyocardium has a markedly lower capillary density, and larger myocyte cross-sectional area, than the epimyocardium. The sarcolemmal-surface/cell-volume ratio is significantly less in endocardial myocytes. No regional differences were found with regard to capillary diameter, interstitial space volume, or volume percent occupied by blood vessels and myocytes. Likewise, there are no differences in proportions of cardiac cell volume occupied by myofibrils (57%), mitochondria (25%), nuclei (1.5%), T tubes (1.2%), and sarcoplasmic reticulum (2.0%). The ratios of surface areas of T tubes and SR to their respective volumes and to cell volumes do not vary with transmural location. The regional differences and similarities are discussed in relation to general problems of blood flow in the heart and cardiac hypertrophy.

Animals↗

Differences in regional capillary distribution and myocyte sizes in normal and hypertrophic rat hearts.

Data are reported which show significant regional capillary differences in left ventricular endocardium and epicardium of normal rats and of rats with hyperthyroid-induced cardiac hypertrophy. The epicardial region of control rats has 38% more capillaries than the endocardial region. Control endocardial myocytes are 62% larger in cross-sectional area than epicardial myocytes. Hypertrophic hearts exhibit regional differences in capillary density similar to those in the normal hearts, but there is an overall reduction of 12 and 17.5% in capillary density in both regions. The average cross-sectional area of myocytes increases 34.5% in the epicardium and 22.5% in the endocardium.

Animals↗