Survival and function of bursa-derived cells in bursectomized chickens

Chicken given heterologous antibodies to μ chains as embryos and again following bursectomy at hatching were rendered permanently agammaglobulinemic, whereas treatment with anti-μ alone resulted in transient hypogammaglobulinemia. These and other observations indicate that sites other than the bursa of Fabricius are unable to serve as sources of immunoglobulin-producing cells. Agammaglobulinemia did not develop in birds bursectomized at 1, 14, or 35 days after hatch during an observation period of 21–125 wk. Some bursectomized birds developed 10 × normal IgM levels but were very deficient in IgG; this pattern persisted throughout life. B lymphocytes, identified by surface immunoglobulins in high density, were permanently deficient in bursectomized animals despite development of hypergammaglobulinemia and high levels of antibodies to ferritin following hyperimmunization. In experiments employing embryonic bursectomy, the level of the circulating pool of B lymphocytes was shown to be dependent upon the time allowed for the bursa to function before removal.     

Cytochemical examination of peripheral blood lymphocytes in bursectomized chickens

The starting material were 86 day-old utility hybrid Tetra SL chicks. Beginning from their third week of life, 59 chickens were kept in two separate rooms "A" and "B" for 42-56 days. The values of temperature and cooling were somewhat different in rooms "A" and "B", however essentially not deviating from the accepted zoohygienic norms. The obtained results revealed a significant reduction of the activity of acid phosphatase in blood lymphocytes of 8-10 week-old chickens bursectomized in the neonatal period and kept in room "A". No such changes were found concerning ATP-ase and 5'-nucleotidase. Similar effect appeared in the lymphocytes of non-bursectomized chickens kept in room "B". Antigen stimulation (SRBC) of bursectomized and non-bursectomized chickens brought about an increased activity of all the three enzymes in blood lymphocytes. At the same time it should be emphasized that the increased activity of the enzymes tested was modulated by bursectomy and conditions of the medium.     

Inability of choleragenoid-sensitized cells to induce T cell-mediated cytolysis.

Murine splenocytes and tumor cells bind cholera enterotoxoid (choleragenoid). Four hours after sensitization, choleragenoid-coated cells were lysed in the presence of anti-cholergenoid serum and complement, indicating that the binding was stable. Choleragenoid-coated cells were unable to sensitize spleen cells from normal or choleragenoid primed syngeneic mice into displaying a cytotoxic effect against choleragenoid-coated target cells in the T cell-mediated cytotoxicity assay. Cells coated with both choleragenoid and trinitrophenyl (TNP) groups did sensitize syngeneic spleen cells to display a cytotoxic effect against target cells bearing choleragenoid and TNP or TNP alone, but not choleragenoid alone. These data demonstrate that the mere binding of a foreign component to lymphoid cells is not sufficient to allow sensitization of cytotoxic T cells.     

The effect of polypeptides from the thymus, bone marrow and bursa of Fabricius on the immunogenesis and hemostasis in neonatally thymectomized and antenatally bursectomized chickens

The effect of polypeptides from the thymus, bone marrow and bursa of Fabricius on immunogenesis and hemostasis was investigated in neonatally thymectomized and antenatally bursectomized chickens. It has been established that polypeptide factors from the bursa of Fabricius have the most pronounced effect on the immunity and hemostasis.     

Inability of chlorophenols to induce 6-thioguanine-resistant mutants in V79 Chinese hamster cells

The induction of mutation at the hypoxanthine-guanine phosphoribosyl transferase locus and cytotoxicities of 6 different chlorophenols (2,4- and 2,6-dichlorophenol, 2,4,5- and 2,4,6-trichlorophenol, 2,3,4,6-tetrachlorophenol and pentachlorophenol) were examined in V79 Chinese hamster cells without exogenous metabolic activation. The chlorophenols were cytotoxic to V79 cells, but failed to produce significant increases in the frequency of 6-thioguanine-resistant mutants.     

Purification of DNA ligase II from calf thymus and preparation of rabbit antibody against calf thymus DNA ligase II

DNA ligase II has been purified about 4,000-fold to apparent homogeneity from a calf thymus extract. The ligase consists of a single polypeptide with a molecular weight of 68,000 as estimated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. On fluorography after electrophoresis, a DNA ligase-[3H]AMP complex gave a single band corresponding to a molecular weight of 68,000. The Km values of the ligase for ATP and nicked DNA (5'-phosphoryl ends) were obtained to be 40 and 0.04 microM, respectively. Antibody against calf thymus DNA ligase II was prepared by injecting the purified enzyme into a rabbit. The antibody cross-reacted with DNA ligase II but not with calf thymus DNA ligase I. DNA ligase II was not affected by antibody against calf thymus DNA ligase I with a molecular weight of 130,000 (Teraoka, H. and Tsukada, K. (1982) J. Biol. Chem. 257, 4758-4763). These results indicate that DNA ligase II (Mr = 68,000) is immunologically distinct from DNA ligase I (Mr = 130,000).     

Estrogen receptors in rabbit thymus

The estrogen receptors presence or absence in the thymus gland represents the basic element to assert or to exclude any estrogenic action in the thymus. Now we have measured the presence of cytoplasmatic estrogen receptors in the female rabbits thymus, using some methods (sucrose gradient, protamine sulphate, dextran-coated charcoal). Finally, we have investigated, using the sucrose gradient assay, the nuclear ER presence in 1000g thymic pellet. The results exclude high levels of estrogen-binding proteins while don't suggest their total absence in the female rabbit thymus.     

Inability of rabbit peritoneal polymorphonuclear leukocytes to synthesize arachidonic acid from linoletc acid

In PMN leukocytes isolated from rabbit peritoneal exudate the major phospholipids were choline phosphoglycerides (40%), ethanolamine phosphoglycerides (26%) and sphingomyelin (20%) with lesser amounts (3–6%) of serine and inositol phosphoglycerides. The essential fatty acid, linoleic acid, predominated (>35%) in each phospholipid except in inositol phosphoglycerides where it was slightly less than arachidonate and in sphingomyelin where saturated acids predominated. However, on a total mass basis there was more arachidonate in ethanolamine and choline phosphoglycerides than in inositol phosphoglycerides. The uptake, incorporation and metabolism of [1-¹⁴C] fatty acids of varying chain length and degrees of unsaturation were examined. All fatty acids were taken up but incorporation of saturated acids varied inversely with chain length. Arachidic acid and trans-isomers of 18:1 and 18:2 were esterified primarily to triacylglycerol whereas phospholipids contained a large portion of the other acids. Icosatrienoic and arachidonic acids were esterified to ethanolamine, serine and inositol phosphoglycerides to a comparatively greater extent, reflecting the normal distribution of these fatty acids. PMN leukocytes had a low capacity for Δ9 desaturation and chain elongation and no Δ6 or Δ5 desaturation could be detected. Thus, PMN leukocytes lack the ability to form arachidonate from 18:2 precursor molecules available in the cellular neutral lipids and phospholipids and arachidonate per se is an essential fatty acid for these cells.     

Inability of [3H]estriol to induce maximal cooperativity of the estrogen receptor

The interaction of [³H]estriol with the partially purified estrogen receptor from calf uterus shows positive cooperativity that is dependent upon receptor concentration and temperature. At a receptor concentration of 1 nM and 25°C the [³H]estriol-receptor cooperativity was low, the Hill coefficient (n_H) was 1.03 ± 0.02; however, with increasing receptor concentrations the receptor's cooperativity increased until at approximately intracellular receptor concentration (20 nM) the n_H = 1.20 ± 0.04. At 0°C and a receptor concentration of 10 nM the [³H]estriol-receptor interaction was highly cooperative, the Scatchard plot was convex and n_H = 1.58 ±0.04 while at 30°C the Scatchard plot approached linearity and n_H = 1.03 ± 0.02. In comparison, [³H]estradiol was capable of inducing, at 0 or 30°C and at a receptor concentration of 1 nM or greater, maximal receptor cooperativity, n_{H = 1.63}.These data demonstrate: (a) the receptor's conformation and binding mechanism change in a specific manner with temperature, so that receptor analysis at 0°C does not necessarily reflect the receptor's properties at biologically relevant temperatures; (b) the dependence of the receptor's cooperativity on receptor concentration, which suggests interaction between dissociable subunits; and (c) the lower cooperativity induced by estriol, in comparison with estradiol, which indicates estriol is less efficient in shifting the receptor toward a higher affinity or the activated state of the receptor.