Search PubMed⌕ Search

Biomedical subjects

T Sasabe

Publications and source records attributed to T Sasabe.

53 records · Page 3Linked to original sources

Interferon enhances the natural killer cell activity of the retinoblastoma patients to autologous retinoblastoma cells.

The cytotoxic activities of the peripheral lymphocytes prepared from two retinoblastoma patients to freshly isolated autologous tumor cells were measured using 51Cr-release assay. The retinoblastoma cells of the two patients resisted lysis by unstimulated effectors, whereas interferon(IFN)-stimulated effector cells gave a significantly higher cytotoxicity. This result implies that IFN therapy may be potent in treating high-risk retinoblastoma patients.

Cytotoxicity, Immunologic↗

Dome formation in cell cultures of chick embryo retinal pigment epithelium and effects of ouabain and 2,4-dinitrophenol thereon.

Cells from chick embryo retinal pigment epithelium were cultured on glass slips. The primary culture cells formed confluent cell layers which were studded with a number of domes. The domes had usually appeared by the fourth day of culture and were susceptible to 3 X 10(-6) M ouabain and 10(-4) M 2,4-dinitrophenol, indicating that fluid was transepithelially transported from the apical to the basal side by means of an energy-requiring and ouabain-sensitive mechanism. Other than domes, small blisters appeared after 4-10 days of culture. They were also susceptible to the metabolic inhibitors.

2,4-Dinitrophenol↗

A newly established cell line of rabbit lens epithelium.

Rabbit lens epithelial cells have been cultured continuously for more than 24 months (200 generations) in monolayers. Their morphology resembled cobblestones when confluent and was spindle-shaped during growth. The doubling time was 40 hours. The cells were capable of colony formation and their plating efficiency was about 6%. They had immunoreactivity to antiserum to the crystalline-rich supernatant of rabbit lens homogenate. Therefore, it was concluded that they were a permanent cell line and they were named TOTL-86 cells.

Animals↗

Natural killer cells kill human retinoblastoma cells.

Human peripheral blood lymphocytes were obtained from healthy individuals and their cytotoxicity against retinoblastoma cells was measured using 51Cr-release assay. The lysis of two human retinoblastoma cell lines, Y-79 and WERI-Rb 1, varied greatly from blood donor to donor, but the lysis of K-562 was very similar among the donors. Furthermore, the lysis of Y-79 was markedly inhibited by the addition of K-562, a natural killer (NK) cell-sensitive target, but not by Raji, an NK-resistant target, suggesting that both Y-79 and K-562 shared a common NK-directed antigen. The major cytotoxic activity was associated with nonphagocytic and nonadherent cells, and it was finally recovered in the low-density fraction which was enriched with large granular lymphocytes. These lines of evidence indicate that natural killer cells (NK cells) in the peripheral blood killed retinoblastoma cell lines. On the other hand, three kinds of retinoblastoma cells freshly isolated from patients were resistant to the lysis by the lymphocytes obtained from the donors with high NK activity. However, these tumor cells displayed an enhanced susceptibility when the effectors from the same donors were treated with interferon. The study of NK cells and the interferon system may shed light on the treatment of retinoblastoma.

Cell Line↗

Fibronectin synthesis by the rabbit cornea: effects of mouse epidermal growth factor and cyclic AMP analogs.

We investigated whether the cornea can synthesize fibronectin which participates in corneal wound-healing. We also examined the effects of epidermal growth factor (EGF) and cyclic AMP analogs on fibronectin synthesis by the cornea. Rabbit corneal blocks were cultured in medium without serum, and the amount of fibronectin in culture medium was determined by ELISA assay. When rabbit corneal blocks were cultured in the medium alone, fibronectin contents in the medium increased with increase in the incubation period. This increase was enhanced by the addition of EGF to the culture medium, and was inhibited by addition of a protein synthesis inhibitor, cycloheximide. The addition of cAMP analogs, 8-bromo cyclic-AMP and dibutyryl cAMP, to the culture medium also increased the rate of fibronectin production by the cornea. These results show that the cornea can synthesize fibronectin and its synthesis is stimulated by EGF and cAMP analogs.

8-Bromo Cyclic Adenosine Monophosphate↗

Hanganutziu-Deicher heterophile antigen in human retinoblastoma cells.

We investigated the possible existence of Hanganutziu-Deicher antigen (HD antigen) on retinoblastoma cells by means of indirect membrane immunofluorescence and a complement-dependent antibody-mediated cytotoxicity test. We prepared antiserum in the chicken by immunization with purified equine hematoside highly specific to HD antigen. Three kinds of retinoblastoma cell lines, Y-79, WERI-Rb 1, and TOTL-1, showed positive membrane staining. Y-79 and TOTL-1 cells were also confirmed by the cytotoxicity test to possess HD antigen. Retinoblastoma cells freshly isolated from two patients had a positive membrane immunofluorescence. These results indicated that HD antigen was expressed in human retinoblastoma cells in vitro as well as in vivo.

Antigens, Heterophile↗

Sodium and chloride transport across the isolated rabbit ciliary body.

Unidirectional Na+ and Cl- fluxes were determined in the isolated rabbit ciliary body under short-circuited conditions. A statistically significant net Cl- flux towards aqueous was detected in the standard bathing solution (HCO3- = 115 mM), but no net Na+ flux was demonstrated in this solution. The net Cl- flux exceeded the short-circuit current, suggesting the existence of a net flux of other ion(s). In a bathing solution containing 5 mM HCO3-, the net Cl- flux was abolished, suggesting that HCO3- in the bathing solution enhances the net Cl- flux.

Action Potentials↗