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Electron microscopy of the body wall of Opisthorchis viverrini shows the integument which is connected to the epidermal cell with fine protoplasmic tubules, to form a syncytium, as in Clonorchis sinensis and other trematodes. Vacuole-like secretory granules are distributed in the matrix of the integument, and mitochondria are arranged at the proximal outer surface of the integument. The crystalline inclusions are observed in the perinucleus of some epidermal cells.

In vitro cell transformation of human embryonic cells could be induced by DNA extracted from virions of SV 40 purified by density gradient centrifugation. The result shows clearly that cell transformation is in· duced by incorporation ofa part of viral DNA into the genome. In addition, for the purpose of clarifing the biological differences between the normal and transformant, the alteration of the cell membrane structures of transformants was observed from the mechanism of phagocytosis. The iron colloid particles are taken up by normal diploid fibroblasts but not by the human and hamster transformants. This fact suggests a difference in the molecular arrangement of the cell membranes between the normal and transformants. In the presence of histones, however, the transformants phagocytize the colloid particles very actively. The results show cell membranes of transformants are altered in the molecular structure responsible for the surface charge.

Japan was the first Asian country to introduce social insurance measures and it has expanded them during the last few decades. The first social insurance law was passed in 1922, dealing with worker's health insurance, and it was followed by the National Health Insurance in 1938, Seamen's Insurance in 1939, and Employees' Pension Insurance in 1921. However, these were seldom widely available in actual practice because of the characteristics of public assistance which limited them to the poor.

The concentration of catalase protein in anemic blood with enhanced population of reticulocytes and in non-anemic blood was determined immunologically by double diffusion test with anti-mome-liver catalase rabbit serum. The change in catalase protein concentration in anemic blood during incubation at 37°C for 24 hours was also studied. It was indicated that the diminished catalase activity in acatalasemic blood was due to the depletion of the protein and that catalase protein in acatalasemic reticulocytes decreased markedly by in vitro maturation. Furthermore, the possible presence of inactive catalase protein in acatalasemic blood was also suggested. Catalase protein concentration of acatalasemic anemic blood decreased by the incubation at 37°C for 24 hours in parallel with the decrease in reticulocyte count and catalase activity, and the decrease in catalase protein concentration of hemolysate by the same incubation parallel with the decrease in catalase activity. It is hypothesized that the unstable catalase protein with genetical change in structure easily decomposes during acatalasemic reticulocyte maturation is presented.

In order to examine how long diploid cells can be maintained in vitro cultivation without any chromosomal aberrations and to evaluate the mechanism of chromosomal heteroploid transformation, changes of chromosomes were studied in the course of serial in vitro transfers in four normal rat liver cell lines. As a result the diploid cells decreased in number gradually at early culture stage and disappeared completely in the periods between 350 and 500 days. The culture shifted to heteroploid as follow: diploidy---tpseudodiploidy---thypodiploidy---thypertriploidy or hypotetraploidy. This proces to heteroploid transformation is divided into five stages according to ploidy: 1- and II-stages show diploidy, III-stage, pseudodiploidy, IVstage, hypodiploidy and V-stage, hypertriploidy or hypotetraploidy. Chromosomal heteroploid transformation and neoploastic conversion occurred in IV-stage of the cultures. A possible mechanism involved in the process of chromosomal transformation was discussed.

Three inoperable patients with primary hepatoma could be placed on gluconeogenic diets (minimum carbohydrate-high fat diets) for one to three months. A transient inhibition or a marked retardation of the tumor growth was observed with these patients and their entire clinical courses were fairly good. These results confirmed our previous observation with a metastatic liver tumor patient.

By subcutaneous inoculation of N, N'-dimethylnitrosourea to adult male C3Hf/Bi mice once a week for 10 consecutive weeks the authors studied the correlation between immunological functions and histological changes in lymphatic tissues at the latent period of thymic lymphoma whose development is known to occur in 100 per cent. As a result, it was found that PFC of the spleen to sheep erythrocytes decreased to about one third the normal level by two weeks, and to one tenth by 8 weeks after initial inoculation of this compound. Hemolysin and hemagglutinin titers of the serum became less than 1 : 2 after 6 weeks and later. As for histological changes in the thymus, disappearance of lymphocytes became marked by 2 weeks, and there appeared tumor cells by 8 weeks. Also the peripheral lymphocytes as well as the total spleen cells decreased in number along with increase of the frequency of inoculation of N,N'-dimethylnitrosourea. These results seem to suggest that the immunosuppressive effect of carcinogen facilitates the development and proliferation of tumor cells possessing tumor specific antigenicity in the course of N, N'-dimethylnitrosourea- carcinogenesis.

As the first step to analyze the autoimmune disease of red cells the recognition mechanism of macrophage to red cells or erythrophagocytosis has been studied in vitro by using mouse peritoneal macrophage and homologous and cells and the following results were obtained: 1. In Hanks solution, the mouse macrophage hardly phagocytizes living red cells, both homologous and heterologous ones. But in the presence of mouse serum, the macrophage phagocytizes heterologous red cells selectively but does not phagocytize homologous ones. 2. The macrophage actively phagocytized homologous red cells prior to treatment with concanavalin A (Con A) at a concentration as low as 1.95 ltg/ml. 3. Red cell agglutination was clearly recognized in those treated with Con A at 62.5 lag/ml or more, but not at 1.95 ltg/ml. 4. The red cell agglutination by Con A was inhibited with D-glucose, D.mannose and a-methyl glucopyranoside at the concentration as low 1.5 mM, while the phagocytosis was suppressed only at a very high concentration of the sugars, 1, 000 mM. 5. Fragility test of the red cells treated with Con A showed a lower resistance of red cells to hypotonic solution than those treated with Con A at the concentration of 31.25 p.g/ml or more 6. Electron microscope observation revealed no membrane damage of red cells by treating with Con A at a concentration of 1.95 ,ag/ml, where erythrophagocytosis was observed. The membrane damage occur. red by treating with Con A at 31.25 ltg/ml or higher. 7. All the data indicate that the phagocytosis of homologous red cells by macrophage is induced by the adherence of a small amount of Con A, which induces no detectable changes of red cell surface and red cell membrane as revealed by agglutination test, fragility test, electron microscope observation and circular dichroism. On the basis of these observations a possible recognition error to homologous red cells by adsorbing a minute quantity of foreign substances on their surfaces has been discussed.

I) On an identified giant neurone of the right parietal ganglion in a snail's subesophageal ganglion-complex, the synaptic contribution to the production of the plateau formation of biopotential or grouped spike discharges of the soma has been studied in the presence of a convulsant. 2) The orthodromic stimulation of a peripheral nerve (the intestinal nerve) can elicit the plateau formation of biopotential, instead of normal spike discharges, in the identified neurone treated with a convulsant. 3) With the application of a convulsant, for example bemegride which was in a concentration less than that necessary to produce the plateau formation, an EPSP accompanied a spike with a constant delay. This EPSP is a product of a proprioceptive reflex arc consisting of two excitatory synapses with a certain subordinate neurone. 4) Later, in the presence of a convulsant, spontaneously conveyed multiple EPSP's were observed on the biopotential of the identified neurone. These multiple EPSP's produced grouped spike discharges or the plateau formation of biopotential of the neurone. 5) The multiple EPSP's may be produced by the grouped spike discharges of the subordinate neurone, the membrane property of which would be changed by a convulsant. It is presumed that the grouped spike discharges or the plateau formation of biopotential often occurs synchron. ously in many neighboring neurones by means of synaptic triggering in the presence of a convulsant.

A method of intracranial transplantation of the tumor induced by adenovirus type 12 in syrian hamster has been described. The incidence of intracranial tumor development was 86 (90.5 %) out of 95 animals and the average survival time and tumor size at death were 15.1 days and 4.1 mm in diameter respectively. The consistency of the days of death after intracranial transplantation of the tumor was remarkable. The transplanted tumors developed preferentially at the site of implantation and tumor cell seeding and tumor growing took place rarely along the ventricular system. Glial or lymphoid cell response to the tumor was not observed at any stage after transplantation in surrounding cerebral tissues of the animals. Histomorphologically, no elementary differences were observed between intracranially transplanted tumors and serially transplanted subcutaneous tumors. These facts permit the system to be applied to an experimental brain tumor model as large-scale testing.

This paper describes various aortic parabiotic procedures and discusses various problems concerning these procedures. The most satisfactory results, nearly 100 % of survival rate, can be achieved using longer sections of aortae of 2 to 5.month old rats. In these rats blood circulation between the parabionts has completely been established.

A subcutaneous tumor of a patient with epidermodysplasia verruciformis was studied by the light microscopy, the electronmicroscopy and the immunofluorescent test. The tumor cells were histologically pleomorphic and electronmicroscopically contained varying amounts of cytoplasmic filaments without Z-band formation. The antimyosin serum stained the tumor cells, showing their myogenic origin. No virus or virus-like particles were observed in the tumor. Tumor antigens stainable by the patient's serum were not detected. Hamsters inoculated with the tumor extract at birth developed no noticeable diseases.

Newborn mice of C3Hf/Bi (Zb) strain were divided into three groups and injected, intracranially with adenovirus type 12 alone, subcutaneously with 20 mgjkg of N, N'-dimethylnitrosourea following intracranial inoculation of adenovirus type 12, and subcutaneously with 20 mgjkg of N, N'-dimethylnitrosourea alone at 10 days of age, respectively. With adenovirus type 12 alone, intracranial tumors were induced in 12 out of the 25 effective animals. With N, N'-dimethylnitrosourea following adenovirus type 12, intracranial tumors were produced in 19 out of the 21 effective animals and these tumors were virus-induced ones. With N, N'-dimethylnitrosourea alone, no intracranial tumors were induced. In control mice, administered subcutaneously with 20 mgjkg of N, N'.dimethylnitrosourea within 24 hr after birth, necrosis of the external granular cells and hypoplasia of the granular layer of the cerebellum was observed.

As a step in the elucidation of human cancer immunity we studied antitumor activity of lymphoid cells by conducting a series of cultures using the primary culture of cells from spontaneous mammary cancers from C3H and RIll mice mixed with autochthonous lymphoid cells, and obtained the following results. 1) With 24 mammary tumors obtained from 24 mammary cancer. bearing mice, we prepared 22 suspensions containing sufficient numbers of free tumor cells, and attempted primary culture with them. As a result we were able to attain satisfactory primary culture cells in 18 trials. 2) With each group of the 18 primary culture tumor cells we conducted mixed cultures with autochthonous lymphoid cells (mainly spleen cells) in proportion of 1 : 40, for 48 hours, and counted viable tumor cells after the culture. As a result it was found that in 11 trials the lymphoid cells showed antitumor activity. In the remaining 7 groups of lymphoid cells there could be observed no antitumor activity, but some of them showed tendency to slightly accelerate the growth of tumor cells. 3) On looking at the correlation between the antitumor activity of lymphoid cells and the ratio of tumor weight/body weight, it was revealed that the antitumor activity is greatest when the tumor is around 10% the body weight, and as the tumor grows larger, such antitumor activity disappears. From these results, it may be concluded that even in spontaneous mammary cancer of mouse, autochthonous lymphoid cells exhibit anti. tumor activity on indigenous tumor, and this seems to indicate that cell. mediated immunity has been established.

By inoculating E. coli B into the semisynthetic medium we conducted shaking culture, and observed alterations of the total phospholipid contents and the amounts of individual phospholipid components in various stages of growth. The results are briefly summarized as follows. 1. The total phospholipid content has been found to be greater during early culture period, while it decreases as the growth age advances. 2. Phosphatidyl ethanolamine gradually increase as the culture period approaches the stationary phase. 3. Phosphatidic acid and phosphatidyl glycerol decrease precipitously as growth age advances. 4. Cardiolipin shows the maximum content in the middle log phase when the growth rate is most speedy.

Circular DNA isolated from human kidney mitochondria was studied by electron microscopy. I. Mean contour length of monomers of the mitochondrial DNA was 4.96 ± SE 0.28 /μ 2. The complex molecules (oligomers) of mitochondrial DNA were observed in frequency of 6.2 per cent. Among them circular dimers accounted for two per cent of all circular DNA molecules. 3. Circular DNA fibers with an intermediate perimeter between the　monomer and dimer, and with a contour length shorter than 3 μ were occasionally observed. 4. Some discussions were made on the emergence of the circular dimer.

Electron microscopic observation of replicating SV 40 DNA has revealed the existence of two types of RF, e form and (1 form. The frequency of RF at 54 hours after infection was 8.9% for the e form and 4.3% for the (1 form. Morphological evidence exhibits that in (1 form RF the tails are, predominantly, shorter than the viral genome and double length SV-40 genomes are also capable of replication in SV-40 infected VERO cells.

The effect of 6.MPR on the antibody formation of rabbits challenged with bovine serum albumin has been studied in comparison with that of 6.MP. Observation revealed that the antibody formation is profoundly suppressed when the animal is treated with 6.MPR in an appropriate dose and period in relation with the introduction of antigen. Discussion was made of the possibility of 6.MPR as a superior therapeutic agent for autoimmune diseases.

Under in vivo conditions JTC-II cells derived from Ehrlich ascites　tumor are led to destruction by lymph node cells by two processes. The　one is the interaction of lymph node cells of the C57BL (♀) mouse sensitized with Ehrlich ascites tumor cells, and the other is the interaction of　normal C57BL (♀) mouse lymph node cells treated with PHA-M. In　these two reaction systems the following differences have become clear. The regional lymph node cells from the C57BL (♀) mouse sensitized　with Ehrlich ascites tumor cells show a marked inhibitory effect on the　growth oflTC-II cells by 10 days after sensitization.　In the observations under the phase contrast microscope these lymph node cells tend to adhere around the antigenic cells by culture hour 5-6, and by culture hour 24-48 they lead the latter to undergo cytolysis. The normal lymph node cells of C57BL (♀) mouse treated with PHA show anti-growth effect oflTC-II cells. PHA-M used proves to be effective in the concentration of 2% (v/v). Likewise after such normal lymph node cells are previously treated with 2% PHA-M for 12 hours, they also inhibit the growth of lTC-II cells when two cell groups are cultured together. In such intercellular reaction between the two cell groups there is no specificity. By observations under the phase contract microscopy, by culture hour 2-3 the adherence and aggregation of lymph node cells begin to occur, and by 18-24 hours of culture the target cells are led to undergo cytolysis. In this instance, lymph node cells are prone to adhere and aggregate on one side of the target cell.

We administered a branched-chain amino acid (BCAA) infusion to 16 patients with hepatic failure and two healthy subjects, and then evaluated its effects on ammonia metabolism and amino acid metabolic pool. Immediately after the BCAA infusion, the venous blood ammonia concentration increased in 12 of 15 patients with hepatic failure and in both two healthy subjects. Glutamine (Gln) also rose in all cases following the BCAA infusion, and this rise was particularly marked in the hepatic failure group. The increase in Gln due to the BCAA infusion and the arteriovenous difference in the pre-administration ammonia concentration showed a good correlation. These results suggest an increase in glutamine cycle capacity in patients with hepatic failure.