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Biomedical subjects

G M Hahn

Publications and source records attributed to G M Hahn.

At least 181 records · Page 10Linked to original sources

Focus formation by a murine sarcoma leukemia virus complex. II. Quantitative aspects of the interaction between radiation leukemia virus and its murine sarcoma virus pseudotype in strain C57BL mouse embryo cells.

A quantitative study has been made of the interactions between radiation leukemia virus (RadLV), its murine sarcoma virus pseudotype, and their C57BL host cells. The elimination of interference phenomena by delayed infection of cells with RadLV made possible the quantitative determination of the pseudotype in terms of defective sarcoma and endogenous RadLV particles. This in turn permitted the quantitative assessment of RadLV helper activity and of the various factors which influence the accuracy and sensitivity of the helper assay.

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Serum concentration: effects on cycle and x-ray sensitivity of mammalian cells.

If the content of serum in the culture medium of exponentially growing Chinese hamster cells is below optimum (15 percent), the doubling time and the resistance to x-irradiation of the cells are increased. In synchronously dividing populations the increase in doubling time is primarily caused by increase in duration of the postmitotic (G(1)) phase of the cells; this phase is relatively radiation resistant. The response of the cells growing synchronously is related quantitatively to the response of the cells dividing randomly.

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State vector description of the proliferation of mammalian cells in tissue culture. I. Exponential growth.

Proliferation of mammalian cells, even under conditions of unlimited growth, presents a complex problem because of the interaction of deterministic and stochastic processes. Division of the cell cycle into a finite number of parts establishes a multidimensional vector space. In this space an arbitrary culture can be represented by a vector called the state vector. The culture's subsequent growth is represented mathematically as a series of transformations of the state vector. The operators effecting these transformations are presented in matrix form and their relationship to the distribution of cell generation times is described. As an application of the model, the growth of an initially synchronized culture is considered and an unambiguous measure of the degree of synchrony is proposed. Results of a computer simulation of such a culture show the behavior with time of the degree of synchrony, the total cell number, and the mitotic index. In particular the importance of the magnitude of the coefficient of variation of the generation time distribution is illustrated.

Animals↗

Temperature distributions induced in pig tissues by a water-cooled disk electrode rf system.

Thermal dosimetry is one of the most challenging and necessary aspects of therapeutic hyperthermia. Treatment optimization and assessment of efficacy of the therapy can only be achieved by a quantification of the thermal distributions in normal and malignant tissue induced by specific configurations of heat sources. Radial and axial temperature distributions induced in normal porcine tissues by a pair of disk-shaped direct contact electrodes operating at 0.5 MHz are presented in this communication. Temperature increments induced in the skin, adipose tissue, and skeletal muscle tissue are correlated with the magnitude of the incident power density for various sizes of circular electrodes. The observed thermal distributions very likely relate to the heterogeneous thermal and electrical properties of these tissues.

Animals↗

Use of N-sigma-dansyl-L-lysine and flow cytometry to identify heat-killed mammalian cells.

We have employed the nontoxic fluorescent membrane probe, N-sigma-dansyl-L-lysine (DL) to study the effect of mild (45.5 degrees C) heat shock on a variety of mammalian cell lines. It has been previously proposed by Humphries and Lovejoy (1983) that DL selectively partitions into (and diffuses through) membranes whose component molecules have undergone lateral phase separation resulting in the formation of phospholipid domains. Excellent flow cytometric resolution of the DL staining cells from several cell lines was obtained by using bivariate (forward angle light scatter versus DL-fluorescence) analysis. Dye uptake and release data as well as measurement of the octanol: water partition coefficient (7.2) all indicated that the stain was likely associated with the plasma membrane. After heating, all cell lines exhibited a time-dependent increase in the fraction of cells stained by DL. Nearly all of the DL-staining cells were propidium iodide and trypan blue excluding. Exclusion of erythrosin B or inclusion of fluorescein showed a better correlation with colony formation, although neither was found to be as effective as DL in estimating cell killing. A comparison of cell survival curves as measured either by colony formation or by the fraction of cells not stained by DL 24 h after heating indicated a good, though not absolute correlation. These results indicate first that DL may have general usefulness as a stain indicating cell death following heat shock, and second, that DL may have utility as a probe of specific membrane damage induced by heat. Our results are consistent with the hypothesis that membrane lateral phospholipid domain partitioning is associated with hyperthermia-induced cell death in mammalian cells.

Animals↗