Search PubMed⌕ Search

Biomedical subjects

W Sawicki

Publications and source records attributed to W Sawicki.

At least 73 records · Page 4Linked to original sources

Application of the optical Fourier transform for analysis of the spatial distribution of collagen fibers in normal and osteopetrotic bone tissue.

Optical Fourier analysis was applied for evaluation of the differences between normal and pathologically changed bone tissue. Collagen fibers were used as markers of bone structure. To prove the usefulness of this technique for objective mathematical analysis of these differences the spatial spatial distribution of collagen fiber bundles was evaluated in normal and osteopetrotic bone. The variation in the spatial distribution of collagen fiber bundles in cross sections of femur diaphyses was evaluated quantitatively by optical diffraction three groups of Fatty Orl-op strain rats, i.e. phenotypically normal animals, osteopetrotic (op/op) mutants and op/op-mutants cured by transplantation of normal syngenic bone marrow. The histological sections of decalcified bone were stained with Sirus-Red and then photographed under polarizing microscope. The Sirus-Red staining was used to enhance the natural birefringency of collagen fibers. Diffractograms obtained from microphotographs of selected bone section areas, i.e. outer and inner circumferential lamellae and haversian bone of normal and cured op/op animals as well as whole cortical bone and woven bone filling the medullary cavities in op/op mutants were analysed separately. Diffractograms contain summarized information on the size and relative position of these structures in histological sections. The radial and angular distribution of light energy were evaluated for each diffractogram with an electronic detector. The obtained distributions were described by several sets of parameters concerning the position, level and shape of local maxima and minima. Out of these parameters five with the highest discriminant power were chosen for further mathematical analysis. This analysis was based on the calculation of the position of centroids in the multidimensional space described by the linear functions of the chosen parameters for each of the evaluated bone section areas. The centroids (mean values of discriminant scores of each group) represent the centers of gravity of the analysed groups, while the separation of the centroids tested by the F-test illustrates the differences between the respective groups of selected bone section areas. A high level of separation of centroids was found when osteopetreotic bone was compared with normal one, what means that the spatial distribution, size and interstructural distances between the collagen fiber bundles in bone tissue in these two groups of animals differ markedly. A similar situation was observed when osteopetrotic bone was compared with bone tissue obtained from op/op mutants cured by transplantation of normal syngenic bone marrow. On the other hand, the level of separation of centroids was low when bone tissue of cured op/op mutants was compared with the control one, a finding which corresponds to the less pronounced histological differences between these two groups of animals. Computer-aided classification on single microphotographs of selected bone section areas to the known a priori type of bone tissue was performed...

Animals↗

Effect of interferon and poly I: C on DNA fiber propagation in L 929 cells.

Autoradiographic analysis of DNA fiber replication was used to measure the rate of DNA propagation, the distances between initiation points of adjacent replicons and the direction of DNA propagation in L929 cells treated with either interferon or poly I: C, or untreated. Poly I:C ceased by 44% the rate of DNA propagation while the interferon had no effect. Poly I:C but not interferon reduced the mean distance between initiation points by 32%.

Animals↗

High-speed autoradiography of 3H-thymidine-labelled nuclei.

High-speed autoradiography with stripping film of 3H-thymidine-labelled cells was tested. The tests involved: (a) various times of immersion of emulsion-covered cell preparations in the mixture of dioxane-PPO-POPOP, at 20 degrees C, (b) exposure of cell preparations and blanks for various times at either -70 degrees C or +20 degrees C, with different humidity levels. Autoradiographs of good quality could be produced by 2-min immersion in the scintillator, exposure time greater than or equal to 1 h at either temperature and relative humidity 20--30%. A linear relationship between autoradiographic efficiency and exposure time of 1--7 h was found at either temperature, although the efficiency of autoradiographs exposed at -70 degrees C was by approximately 30% higher than that of autoradiographs exposed at +20 degrees C. Background values of autoradiographs dried with a fan and exposed for 1/4--7 h at either -70 degrees C or +20 degrees C were 0.6--0.8 grain/100 micron2. Theoretical calculations and experimental data showed that high-speed autoradiographs are 30--50 times more efficient as compared with conventional stripping film autoradiographs, thus allowing a shortening of the respective exposure time. Theoretical aspects of efficiency and resolution of high-speed autoradiography are considered.

Autoradiography↗

Spatial distribution of DNA-synthesizing cells in colonic crypts of the guinea pig.

The ascending colon of a guinea pig injected with tritiated thymidine was cut serially, autoradiographed and stained with periodic-acid Schiff-hematoxylin. Maps of transversely sectioned crypts were prepared with the use of a microscope eye-piece projector. The number and angular positions of pulselabelled (DNA-synthesizing) cells around the circumference of transverse sections of the crypt were recorded. A method of 'statistics of the circumference' was applied in order to find the variances of angular distances between labelled cells and thereby to find the type of arrangement of DNA-synthesizinbg cells in the crypt. The spatial distribution of DNA-synthesizing cells both around the crypt circumference and along the crypt, was found to be non-random. While the pattern of non-randommess around the crypt circumference is such that the DNA-synthesizing cells tend to occupy positions in the crypt circumference at maximal distances from each other, DNA-synthesizing cells along the crypt tend to occupy positions at minimal distances from each other. DNA-synthesizing cells are arranged in the crypt in rows, each consisting of several cells and each parallel to the long axis of the crypt. Apparently the dividing cell of the crypt produces either two proliferating or two differentiating cells. No evidence of differential mitosis could be found.

Animals↗

Lamina propria macrophages of intestine of the guinea pig. Possible role in phagocytosis of migrating cells.

The macrophages of lamina propria were commonly found both in the small and the large intestine of guinea pigs, mice, rats, and in human duodenum. The frequency of macrophage occurrence was highest in the lamina propria of villous apices of the small intestine and beneath the lining epithelium of the large intestine. In the cytoplasm of lamina propria macrophages localized in those regions, Feulgen-positive (DNA-containing) granules could be observed particularly in the guinea pig intestine. Autoradiography of the latter, 3 to 5 days after [3H]thymidine injection, showed the coincidence of occurrence of labeled Feulgen-positive granules in the macrophage cytoplasm with the appearance of labeled epithelial cells and sheath-fibroblasts in the region of lamina propria containing the highest accumulation of macrophages, i.e., at the apices of villi of the small intestine and beneath the lining epithelium of the large intestine. Labeled nuclei of macrophages were observed scarcely and much less frequently than were labeled cytoplasmic granules. No labeled Feulgen-positive granules could be seen in macrophages 1/2 hr, 1, 2, and 7 days after [3H]thymidine injection. It is suggested that the lamina propria macrophages may play a role in the phagocytosis of some migrating cells of the intestinal mucosa, most probably of the sheath-fibroblasts and/or intraepithelial lymphocytes.

Animals↗

Effect of poly I:C on cell proliferation in vivo.

Female Swiss albino mice were injected intraperitoneally with poly I:C1 microgram/g body weight. The animals were killed 2, 12, and 24 hr after the injection of poly I:C. Half an hour before the death of animals they were reinjected intraperitoneally with 3H-thymidine. Fragments of ileum were excised. The quantification of autoradiographs included the counting of labeled cells, mitotic cells as well as the recording of cell position along the ileal crypts. The spatial distribution of both the mitotic and DNA-synthesizing cells of colonic crypts were affected by poly I:C at neither of time intervals between the injection and the death of animals. On the other hand, the parameters of cellular proliferation, i.e. mitotic and labeling indices, decreased significantly 12 and 24 hr after the injection of poly I:C, being unaffected 2 hr after the injection.

Animals↗

Nonrandom distribution of goblet cells around the circumference of colonic crypt.

The ascending colon of the guinea pig was cut serially and stained with the periodic-acid-Schiff-hematoxylin method. Maps of transversely sectioned crypts were prepared using a microscopic eye-piece projector. The number and angular positions of goblet cells were mapped around the circumference of transverse sections of the crypt. A method of the "statistics of the circumference" was introduced in order to assess the pattern of distribution of goblet cells. This distribution was found to be significantly nonrandom. The nonrandomness is such that the goblet cells tend to occupy positions of the crypt circumference in maximal distances from each other.

Analysis of Variance↗