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F J Förster

Publications and source records attributed to F J Förster.

At least 19 recordsLinked to original sources

Long-term tissue culture of epithelial-like cells from human skin (NCTC strain 2544). II. Viscosity changes after enzyme treatment.

Human skin epithelial-like cells (NCTC strain 2544) were grown in NCTC 135 medium. Neuraminidase and hyaluronidase were added to the growth medium. Cells were incubated 96 h at 36 degrees C. Growth rate and viscosity of cell suspensions were measured after forming single cells mechanically (mopping). With addition of neuraminidase and hyaluronidase, respectively, the growth rate remains unchanged. With neuraminidase a distinct raise in viscosity was achieved, whereas with hyaluronidase only a small effect was seen. The characteristic structure viscosity is maintained in all forms of the viscosity curves at different shear-rates.

Animals↗

Long-term tissue culture of epithelial-like cells from human skin (NCTC strain 2544). I. Measurement of viscosity.

Viscosities of cell suspensions of human skin epithelium (NCTC strain 2544) were determined by a Wells-Brookfield rotation viscosimeter. A structure viscosity may be postulated by the form of the viscosity curves at different shear-rates. At a cell number of 0.5 X 10(6) cells/ml a viscosity of 1.094 centipoise (25degrees C, shear-rate 230 s-1) could be found. Since a suspension of single cells may be easily formed mechanically (mopping) the NCTC 2544 cells are useful as investigational model regarding the investigation of membrane characteristics.

Cell Membrane↗

Separation, isolation, and amino acid composition of the albumin-like fraction from psoriatic scales.

The albumin-like fraction of psoriatic scales was isolated either directly by slab gel electroporesis or after previous treatment with polyethylene glycol6000. After both isolation procedures the amino acid composition was determined. Both proteins were rich of glutamic acid, glycine, and alanine. On the other hand both contained very small amounts of cysteine and tyrosine. Only after the direct isolation procedure the amino-sugar galactosamine could be detected.

Albumins↗

Histophysiology of the vegetative peripheral nervous system of skin.

Preterminal nerve fibers of the peripheral vegetative nervous system make inmediate contact (neuro-effector-areas) to interstitial cells (I.C.). This connection is characterized through a common glycocalyx with the nerve fiber. The I.C. are specific innervated cells and differ morphologically from Schwann-cells, fibrocytes, and histiocytes. The I.C. are able to come into morphologically different contacts with neighbouring cells by microvilli-like cell protrusions. These neighbouring cells then are able to contact other cells by themselves. The results are interpreted in the sense of electro-mechanical feed-back system of information processing in the vegetative periphery.

Animals↗

Subcellular distribution of phosphatases, proteinases, and ribonucleases in normal human stratum corneum and psoriatic scales.

The subcellular distribution of phosphatases, proteinases, and ribonucleases of normal human stratum corneum and psoriatic scales was determined after differential centrifugation. All psoriatic enzymes showed much increased activities as compared to the normal stratum corneum enzymes. The highest activities of alkaline phosphatase from psoriatic scales could be detected in the nuclear fraction. The main activities of all other tested phosphatases and proteinases were present in the cytoplasmatic fraction. The subcellular distribution of the ribonucleases varied according to the pH value.

Alkaline Phosphatase↗

Separation of deoxyribonucleases (DNases) of normal human stratum corneum and psoriatic scales by micro-disc-electrophoresis.

Normal stratum corneum and psoriatic scales were homogenized and a differential centrifugation was performed. The DNase activity of the individual fractions was investigated by micro-dis-electrophoresis. At pH 5 only in the 600xg pellet and 105.000xg supernatant of normal keratin DNase activity could be observed. However, all psoriatic fractions showed distinct enzyme activities. At pH 7.4 little psoriatic DNase activity could only be demonstrated in the 105.000xg supernatant. Except from the 15.000xg pellet all fractions of normal stratum corneum displayed marked activities. In addition the 105.000xg supernatant showed two different DNase bands.

Deoxyribonucleases↗

Histophysiology of mast cells in skin and other organs.

Our observations demonstrate an intimate relationship between peripheral nerve fibers and mast cells. In addition, mast cells in various organs influence both the small blood vessels and the organ parenchyma cells. These relations are interpreted in the sence of a neuro-hormonale feedback-system.

Animals↗

[Isolation and amino acid composition of two pathologically augmented proteins from psoriatic scales (author's transl)].

Two protein bands of water soluble extracts of psoriatic scales, which appear intensified in disc-electrophoretical separation, were isolated and their amino acid compositions were determined. It could be demonstrated that band 9 was rich of glycine, alanine, aspartic acid, leucine, and serine and that band 10 was rich of glycine, threonine, and serine. Both proteins contained an amino-sugar (galactosamine).

Alanine↗

Separation and molecular weight estimation of phosphatases in psoriatic scales by disc-electrophoresis.

Disc-electrophoretic investigations of psoriatic scale homogenates (15000 x g supernatant) revealed several different phosphatase activities. At pH 5 either five different phosphatase active bands (substrates: p-nitrophenylphosphate, naphthylphosphate) or three different bands (substrate: glycerophosphate) could be obtained. At pH 7 only one band (substrate: p-nitrophenylphosphate) showed phosphatase activity. At pH 9.9 either two bands (substrate: p-nitrophenylphosphate) or three bands (substrate: glycerophosphate) could be demonstrated. the acid p-nitrophenylphosphatase activity of the psoriatic specific bands "9" and "10" could be distinguished by their different fluoride and tartrate susceptibility. Also the alkaline glycerophosphatase activities could be differentiated by distinct Ca and Mg susceptibility.

Acid Phosphatase↗

Relationships between mast cells and preterminal nerve fibers.

The observations demonstrate that mast cells do not only show intimate morphological associations to peripheral nerve fibers but also contact basement membranes of capillaries and cell surface coats of organ parenchyma cells. Interpreting these results as a neuro-hormonale feedback system mast cells might be regarded as both receptor organs and regulators of metabolism.

Animals↗

[Histophysiology of the peripheral vegetative system. With special reference to mast cells].

Basallaminae of Schwanncell ensheathed axons and "naked" axons respectively have contact areas between the endformation of the peripheral vegetative nervious system and gröundsubstance. The latter, however, merges directly in the glycocalyces of connective tissue cells and organ cells. These cells may be related to one another (i.e. microvilli, cell processes, glycocalyces etc.) or will form "neuroeffector areas" together with pre- and terminal peripheral vegetative nerve fibers. On the other hand axon swellings might discharge their neurotransmitter substances into the ground substance in such way the neighbouring cells might be influenced ("synapse on distance"). Mast cells may act as regulators of the relationships in the groundsubstance. This because of the connections of mast cells with the peripheral nervous system and consequently with the CNS and the hormonale system. Thus the vegetative periphery as a whole would form a functional unit.

Adult↗