Biomedical subjects
Publications and source records attributed to D F Parsons.
We now have the tools to quantitate and correctly interpret the size, shape, and distribution of organelles in cells. It appears likely that the results will require some changes in some basic assumptions of ultrastructural cytology. This should also result in some new biochemical hypotheses about control of cell metabolism.
Intragastric feeding of dimethylbenz-[a]anthracene in corn oil together with urethane in the drinking water and forced breeding were successful in rapidly inducing (2-4 months) mammary tumors (adenoacanthomas) in inbred NYLR/Nya mice, which have a low incidence of spontaneous breast tumors and of other tumors. The tumors could be quickly and permanently transformed to an ascites form by intraperitoneal inoculation of enzyme-dissociated cells and subsequent serial passage of free cells. Only 10 (3 in some cases) serial passages were required, thus conveniently providing multiple isogeneic carcinoma cell lines in this strain of mice. Some tumor cell lines proliferated strongly in the abdominal cavity even on the first passage.
The differentiation of epithelial tissue in organ cultures of murine buccal mucosa, various human oral mucosa, and human newborn foreskin was found to be dependent on the calcium concentration of the culture media. In low calcium medium (less than or equal to 0.07 mM) epithelial differentiation was inhibited. The original stratifying layers separate and can be removed, producing a destratified explant. Histologically such an explant consists of a dorsal epithelial layer of basal keratinocytes resting on an intact basal lamina with subjacent stroma. At 0.01 mM calcium, the epithelial layer was one to two cells thick whereas at 0.07 mM it could be three or more layers in thickness with the most superficial cells being spread over the underlying cells. In addition to differentiation, keratinocyte migration over the sides of the explant (epiboly) and epithelial proliferation as determined by [3H]thymidine autoradiography were reduced by culture in low calcium medium. Redifferentiation occurs upon return to normal calcium levels (1.8 mM); addition of hydrocortisone to low calcium media was found to facilitate this redifferentiation.
Structural changes of carcinoma cells and fibroblasts migrating through small spaces in the elastic-collagen reticulum of mouse peritoneum have been studied by high-voltage electron microscopy of serial thick sections and by computer graphics reconstruction of cell profiles. The change of shape profile of an individual cell, between serial sections is large and the distribution of organelles is very non-uniform and changes markedly between sections. Conclusions about adhesion, intercell contact, cell shape and polarization of cytoplasmic organelles could only be reached by assessing a complete set of serial sections. Our preliminary results suggest that interesting structural changes occur in both carcinoma cells and fibroblasts when migrating through this tissue.
An invasion model designed specifically for studying mechanisms of invasion of squamous-cell carcinomas was developed with murine buccal mucosa as the host tissue. The mucosal explants were destratified by growth in low-calcium medium (less than 0.07 mM), which results in a dorsal surface composed of one or two layers of basal epithelial cells. The explant has a three-dimensional histoarchitecture similar to in vivo mucosa. A spontaneously transformed epithelial cell line (Pam 27; Yuspa , S. H., Hawley -Nelson, P., Koehler , B., and Stanley, J. R. Cancer Res., 40: 4694-4703, 1980) was used to seed explants. Attachment and subsequent growth and invasion were monitored. The morphology of attachment was examined by conventional and high-voltage electron microscopy. In addition, attachment was quantitated by using [125I]iododeoxyuridine-labeled tumor cells. Attachment was shown to be an active process which involves an interdigitation of tumor-host cell processes. Junctional complexes were also observed between tumor and host epithelial cells. By 24 hr, tumor cells were spread on the basal cells and were in the process of replacing host cells. Long-term growth of explants showed that tumor cells can repopulate the epithelial surface and invade the stromal region.
A carcinoma invasion system (Krebs-2 and Ehrlich tetraploid ascites tumors invading mouse peritoneum) was studied by high-voltage electron microscope (HVEM) stereoscopy, conventional (medium voltage) electron microscopy (MVEM), and cytochemistry. Tumor cells entered areas of peritoneum (mainly parietal) only where mesothelial cells were damaged and where there was inflammation of the underlying stroma. The initial invasion was different from that of most other invading carcinomas in that there was minimal breakdown of basal lamina and collagen. Neither tumor cells, inflammatory leukocytes nor peritoneal fibroblasts showed significant secondary lysosome production or release of intracellular or extracellular acid phosphatase. Morphological and cytochemical criteria suggest that in some invading carcinomas, as with non-tumor migrating cells such as leukocytes, widespread proteolysis due to diffusion of proteases is not a prerequisite for invasion of stromal connective tissue.
Dark cells (DC) could be reproducibly demonstrated by differential toluidine-blue staining and electron microscopy (EM) of NYLR/Nya 16- to 19-day embryo and new born skin and phorbol ester-treated or untreated young adult skin. High-voltage electron microscopy on the same or adjacent sections showed that toluidine-blue staining picks out some but not all the DC seen by EM. The ultrastructure of DC was similar in all the above situations, except that phorbol ester-induced DC showed a less contracted nucleus. No support was obtained for DC as stem cells either for basal-cell hyperplasia or for development of hair follicle or gland outgrowths. Most of the severely contracted DC (Types 3 and 4) were assumed to have undergone an apoptotic type of cell death. Two phenomena that may have caused the contraction and apoptosis were observed. Formation of a "contraction vacuole" adjacent to the DC probably led to a loss of intercellular communication. An apparent necrosis of dermal capillaries in areas of abundant follicle downgrowth probably produced local anoxia. Further characterization of DC requires a search for cytochemical or immunologic markers, analysis of intracellular calcium and other elements, and the cloning of subpopulations of basal cells that can be selectively induced to form DC.
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Analysis of electron diffraction patterns from rat hemoglobin taken at 200 kV on a wet stage yields intensity data to a resolution of 2-3 A which are as reproducible as those from typical X-ray diffraction. Some crystals were so similar that the differences in measured intensities were insignificant (R = 0.056), but in other cases real differences between crystals were observed (R = 0.33). Dynamic scattering was insignificant under our diffraction conditions; however, exposures to electron doses as low as 10(-2) e/A2 produced detectable changes in measured intensities. Limits to the reproducibility of the data are set by radiation damage and errors in microdensitometry.
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Interaction of Krebs-2 and Ehrlich tetraploid cells with NYLR/Nya mouse peritoneum mesothelium and penetration of basal lamina and elastic reticulum were studied. Invasion of abdominal viscera was rare. Invading cells had a shrunken nucleus and cytoplasm like the "dark cells" of hyperplastic epithelia. High-voltage electron microscope stereoscopy showed that invasive cells pass through small holes in the elastic reticulum by adherence to the reticulum and by constriction of the cells. High voltage electron microscopy stereoscopy of collagen fibers near tumor cells indicated that fragmentation and loss of collagen is minimal. Rapid progression by ascites transfer appears to produce anchorage-independent cells adapted to ascites fluid growth, but new selection steps must be adopted to concentrate strongly invasive subpopulations.
A differentially pumped environmental chamber, or DIFPEC, has been developed for the AEI EM7 1.2 MV HVEM. The chamber is suitable for imaging and diffraction studies and is capable of operation at pressures approaching one atmosphere. Any mixture of gases can be used including water vapor supplied from an internal reservoir. Correct operation is demonstrated by measurements of temperature, pressure, and water consumption. High resolution (0.2 nm) diffraction patterns were recorded from unfixed, unstained, fully hydrated catalase crystals. This is good functional test of DIFPEC operation and specimen preparation because catalase disorders irreversibly of exposed to less than 95% relative humidity. High- and low-angle diffraction patterns were recorded from unfixed, unstained, fully hydrated rat hemoglobin crystals. All patterns were recorded using 10-4 C/cm2. Whole cell mounts prepared in different ways were imaged and show that 5.3 kPa of nitrogen gas has no detrimental effect on image contrast or resolution. The column vacuum and differentially pumped volume pressure were measured for a number of pumping configuration, as well as for several gases and pressures in the specimen volume. The pressure in the high vacuum portion of the objective lens gap is conductance-limited when the DIFPEC is in place.
A user evaluation has been made by electron microscopists of an X-ray film for routine electron microscopy. The recent improvements in mammographic X-ray films, with the attempt to reduce the patient dose required to produce a high-resolution mammogram, have resulted in some useful films for medium- and high-voltage electron microscopy. They can yield essential cytological information with a reduction of the electron fluence (exposure) applied to the specimen of more than an order of magnitude compared with conventional electron-microscope films. Their use is indicated in situations where beam damage is severe.
Levels of impairment of electron-microscopic images of biological specimens stemming from radiation damage are assessed in a rapid visual procedure that involves taking a pair of low-fluence micrographs of a specimen area before and after a fraction of the picture area has been more seriously damaged by applying a measured electron fluence. The pair of micrographs is treated as a mock-stereo pair and is given contrasting colours. Lateral displacements of specimen details appear as false relief and changes in electron lucency as false colour.
X-ray (CuKalpha) scattering curves of rat liver mitochondria are characterized by continuously decreasing intensity from 0.5 to 5 mrad and a broad maximum centered near 20 mrad. The condensed-to-orthodox morphological transition of the inner membranes of intact mitochondria causes a dramatic decrease in scattering at very small angle and a marked shift of the 20 mrad maximum to smaller angle. A similar small-angle scattering maximum is observed with inner mitochondrial membrane fractions prepared by digitonin treatment and osmotic shock/step gradient centrifugation procedures. However, the small-angle X-ray scattering curves of mitochondria after acetone treatment and osmoticlysis/sonication are essentially continuous. These characteristics of mitochondrial X-ray scattering are discussed in terms of known structural features of the organelle.
Small-angle X-ray scattering data suggest that major but reversible rearrangements of mitochondrial inner membrane structure are induced by uncouplers. Low levels of 2,4-dinitrophenol (10 micronM) cause a perceptible wide-angle shift of the 20 mrad X-ray scattering maximum characteristic of intact liver mitochondria. Higher dinitrophenol concentrations (greater than 25 micronM) reduce this scattering maximum to one-third its initial intensity. In terms of mitochondrial function, the former scattering change appears to correlate with the uncoupling of oxidative phosphorylation while the latter occurs in the course of dinitrophenol stimulation of mitochondrial ATPase activity.
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