Natural antibodies to human retrovirus HTLV in a cluster of Japanese patients with adult T cell leukemia

Human T cell lymphoma leukemia virus (HTLV) is a human retrovirus (RNA tumor virus) that was originally isolated from a few patients with leukemias or lymphomas involving mature T lymphocytes. Here we report that the serum of Japanese patients with adult T cell leukemia, but not the serum of tested normal donors, contains high titers of antibodies to HTLV. These observations, together with data from Japan showing that adult T cell leukemia is endemic in southwest Japan, suggest that HTLV is involved in a subtype of human T cell malignancy, including Japanese adult T cell leukemia.     

Critical water content and water stress coefficient of soybean (Glycine max [L.] Merr.) under deficit irrigation

The objective of this research was to investigate the critical water content (θ _c) and water stress coefficient (K _s) of soybean plant under deficit irrigation. This research was conducted in a plastic house at the University of Lampung, Sumatra in Indonesia from June to September 2000. The water deficit levels were 0–20%, 20–40%, 40–60%, 60–80%, and 80–100% of available water (AW) deficit, arranged in Randomized Completely Block (RCB) design with four replications. The results showed that the soybean plant started to experience stress from week IV within 40–60% of AW deficit. The fraction of total available water (TAW) that the crop can extract from the root zone without suffering water stress (p) was 0.5 and θ_c was 0.305 m³ m⁻³. The values of K _s at p=0.5 were 0.78, 0.86, 0.78, and 0.71 from week IV to week VII, respectively. The optimum yield of soybean plant with the highest yield efficiency was reached at 40–60% of AW deficit with an average K _s value of 0.78; this level of deficit irrigation could conserve about 10% of the irrigation. The optimum yield of soybean plant was 7.9 g/pot and crop water requirement was 372 mm.     

Alteration of release and role of adenosine diphosphate and thromboxane A2 during collagen-induced aggregation of platelets from cattle with Chediak-Higashi syndrome

OBJECTIVE: To compare the interaction of endogenous ADP with collagen and thromboxane A(2) (TXA(2)) during collagen-induced platelet aggregation between platelets from healthy cattle and those with Chediak-Higashi syndrome (CHS). POPULATION SAMPLE: Platelets harvested from blood samples from healthy Japanese Black cattle and those with CHS. PROCEDURES: Aggregation of gel-filtered platelets; release of ATP-ADP; and generation of thromboxane B(2) (TXB(2)), a metabolite of TXA(2), were measured. RESULTS: The potency of collagen to induce aggregation in platelets of cattle with CHS (ie, CHS platelets) was less than a tenth of that in platelets of healthy cattle (ie, control platelets). Platelet aggregation induced by collagen at an intermediate concentration depended on the coexistence of ADP and TXA(2), suggesting that released ADP cannot cause platelet aggregation by itself. Collagen-induced ADP release was markedly decreased, whereas TXB(2) production was slightly low in CHS platelets, compared with that in control platelets. A combination of subthreshold amounts of ADP and 9,11-dideoxy-9alpha, 11alpha-methano-epoxy-prostaglandin F(2) (U46619), a TXA(2) analogue, caused platelet aggregation. Similarly, a combination of subthreshold amounts of collagen and ADP caused platelet aggregation, whereas collagen and U46619 were not synergistic. CONCLUSIONS AND CLINICAL RELEVANCE: Deficient ADP release ensuing from the delta-storage pool deficiency in platelets from cattle with CHS resulted in reduction of collagen-induced platelet aggregation, through attenuation of synergism between TXA(2) and ADP and between ADP and collagen. Furthermore, results of the study reported here indicated that TXA(2) was important for aggregation of bovine platelets.     

Immunoglobulin M associated with secretory component and immunoglobulin A deficiency in bovine colostrum.

Immunoglobulin (Ig) M purified from bovine colostrum was examined by an immunodiffusion analysis with antisecretory IgA serum and was found to be associated with a secretory component. Some of the combined proteins were dissociated if treated with 5 M guanidine-HCl and others were not. Another immunodiffusion analysis of 23 specimens of colostrum led to the finding that certain colostrums were deficient in IgA, even though they contained IgG and IgM.     

Localization of aquaporin water channels in the airway of the musk shrew (Suncus murinus) and the rat

Aquaporins (AQPs) constitute a family of water channels that facilitate membrane water permeability in various tissues of animals. In this study, we compared the expression and localization of AQPs in the respiratory system of the musk shrew (Suncus murinus), which is an insectivore, and the rat by immunohistochemical methods. In both the musk shrew and the rat, AQP1 was expressed throughout the airway in endothelial cells of subepithelial blood vessels and in nasal submucosal fibroblasts. AQP3 and AQP4 were detected in neither the epithelium nor the subepithelial layer of the musk shrew airway, but were abundant in the rat airway epithelium. Musk shrew AQP5 was distributed in the superficial epithelial cells facing the airspaces and in submucosal glandular cells, but, unlike in the rat, not in lung alveolar cells. Additionally, the expression patterns of AQP4 and AQP5 of the musk shrew were partly similar to those of the human previously reported, absence of AQP4 and presence of AQP5 in the upper airway. The expression differences of AQPs between species in the airway indicate that the physiological importance of each AQP may be different in each species.     

Angioarchitecture of the Branchial Arterial System of Carp (Cyprinus carpio L.)

The arterial system of the gills of carp and its histological structure were studied light and electron microscopically by making Mercox or Neoplane Latex corrosion cast preparations. Four pairs of afferent and efferent branchial arteries, and a pair of afferent and efferent pseudobranchial arteries were identified in the branchial arterial system. The 1st and 2nd afferent branchial arteries are given off directly from the ventral aorta, and the 3rd and 4th afferent arteries originate from their common trunk, which is branched off from the ventral aorta caudal to the origin of the former branchial arteries. Numerous afferent filamental arteries are connected to the lamellar blood capillary networks in the gill lamellae via afferent lamellar arterioles, and efferent filamental arteries followed the efferent lamellar arterioles are converged into four efferent branchial arteries that are connected to the dorsal aorta. To the pseudobranchia, afferent pseudobranchial arteries are connected with the ventral branches of the 1st efferent branchial arteries to provide arterial blood to the organ through the afferent mandibular arteries. Afferent pseudobranchial lamellar arterioles originating from the afferent pseudobranchial filamental arteries are connected with the blood capillary networks in the pseudobranchial lamellae, and blood in the capillary networks is drained into the efferent pseudobranchial filamental arteries via 2-4 pseudobranchial lamellar arterioles. Branches of the efferent pseudobranchial filamental arteries are connected with the arteries to the eyeballs and provide blood to choroid of the vascular tunic of them. Pseudobranchial cells surrounding lamellar capillaries in the pseudobranchia are furnished with abundant mitochondria and tubular structures, and the histological findings suggest the cells may share an ability to exchange physiological materials between the cells and the blood in the capillary networks of pseudobranchia.     

Aggregability and post-transfusion survival of canine platelets in stored whole blood

The effects of whole blood storage time on platelet aggregation and on post-transfusion platelet survival time were assessed in dogs. Citrate phosphate dextrose adenine-1 (CPDA-1) was used as a blood cell preservative. Storage time dependent decay of platelet aggregability was assessed. Platelet aggregation responses to collagen and ADP were maintained for at least 8 hr at room temperature. During blood storage, immunoglobulin became nonspecifically bound to platelets, suggesting the potential for immune destruction of platelets by the mononuclear phagocyte system after transfusion. To assess this assumption, the survival times of infused platelets, which were stored for 0 to 8 hr in whole blood, were measured. Post-transfusion survival of platelets was not affected by these storage times. These results suggest that canine platelets maintain viability when stored at room temperature for up to 8 hr in CPDA-1 treated whole blood intended for transfusion.     

Decrease in erythrocyte survival in Theileria sergenti-infected calves determined by non-radioactive chromium labelling method.

Pathogenesis of anemia in the calves infected with Theileria sergenti was investigated from the viewpoint of erythrocyte survival decrease in the circulating blood. For investigation of erythrocyte survival a method of erythrocyte labelling with non-radioactive chromium (50Cr) was utilized. It was found that (1) the erythrocyte survival decreased markedly in the T. sergenti-infected calves compared with that in the uninfected calves; the survival rate of 25.7% for infected calves and 86.0% for uninfected ones on the fourth day after re-introduction of the labelled erythrocytes into the original donors, and that (2) the survival of non-parasitized erythrocytes in the infected calves was also decreased, which indicates no obvious relationship between parasitism and decrease in survival of erythrocytes.     

Release of dopamine and ATP from PC12 cells treated with dexamethasone, reserpine and bafilomycin A1

The amounts and time courses of dopamine and ATP released from perfused PC12 cells were examined using a simultaneous on-line recording system. High KCl (60 mM) caused dopamine and ATP release with similar time courses. The relative amount of dopamine to ATP in the effluent was 9.5. In PC12 cells cultured with dexamethasone, reserpine or bafilomycin A1 for 2 days, these drugs did not affect increases of intracellular Ca2+ in response to high KCl. Dexamethasone doubled the amount of dopamine release induced by high KCl without changing the amount of ATP release. High KCl failed to cause dopamine release in reserpine-treated cells but evoked ATP release. Bafilomycin A1 decreased both high KCl-induced dopamine and ATP release. The ratio of released ATP to total adenine nucleotides and adenosine in response to high KCl was not changed by treatment with the drugs. These results suggest that dopamine and ATP are simultaneously released from secretory vesicles of PC12 cells, in which they are stored via different pathways. Similar to dopamine uptake into secretory vesicles, the H+-gradient across the vesicular membrane developed by vacuolar ATPase may play an important role in the vesicular uptake of ATP.