Physiology of receptor capping induced by erythrocyte surface antigens

The capping of antigen-binding cell receptors by bound sheep erythrocytes (SRC) demonstrates that antigen mounted on a cell surface can generate a signal leading to the capping reaction. SRC-induced capping of ABC is: (a) highly dependent on both aerobic and anaerobic glycolysis, (b) unaffected by agents altering intracellular cyclic nucleotide concentrations, (c) slightly more vigorous in strain A than in CBA mice, (d) inhibited by calcium ionophore, (e) inhibited by the local anesthetic dibucaine and the tranquillizer chlorpromazine, (f) dependent on cytoskeletal activity (i.e., inhibited by the simultaneous presence of colchicine and cytochalasin B), (g) not dependent on the membrane ATPases inhibited by ouabain, (h) not dependent on motility, in that agents which inhibit motility (cytochalasin B alone) or stimulate motility (carbachol) do not alter capping behavior. These properties represent similarities between the capping of surface Ig by the cellular antigens on SRC and by proteins such as anti-Ig. SRC-induced capping is much slower than anti-Ig-induced capping, and only engages 30–40% of ABC, indicating that the nature of the crosslinking agent can influence the kinetics and extent of capping. But SRC cap with the rapid kinetics typical of anti-Ig-induced capping if the surface membrane of the ABC is first cleared of other glycoproteins with trypsin. The removal of negatively charged sialic acid residues by neuraminidase has no such effect. It is probable that the compression of bound SRC into a small area of the membrane requires more energy than does the capping of protein ligands, and that some cells cannot muster enough energy to achieve it.     

Alteration of free serum amino acids in voles infected with Trypanosoma brucei gambiense.

Free serum amino acid pools of field voles, Microtus montanus, were determined over a 24 hr period, and compared to values obtained from voles infected with Trypanosoma brucei gambiense. The majority of amino acids in the control animals demonstrated a diurnal variation, peaking predominantly during the dark portion of the photoperiod. This trend was not evident in the infected animals. In addition, infected voles possessed an apparent state of hypoaminoacidemia, with levels of threonine, serine, valine, isoleucine, leucine, tryosine, and tryptophan typically below uninfected values. Alanine and proline, in contrast, were markedly increased at certain time points. Tyrosine (reduced by approximately 50%) and tryptophan (reduced to levels below detection) underwent the most pronounced drop in trypanosome-infected animals, indicating the possibility of a related alteration in pools of derivative biogenic amines in other tissues. This suggests a role for the latter 2 amino acids in the neuropsychiatric syndromes of African trypanosomiasis.     

Variation in nickel accumulation in leaves,reproductive organs and floral rewards in two hyperaccumulating Brassicaceae species

Understanding the regulation of calcium uptake, xylem transport and its impacts on growth and leaf gas exchange is a subject that has received insufficient recent attention. Calcium (Ca) is unique within the group of key elements required for plant growth in that it also has a role in cellular signalling via regulation of changes in its cytoplasmic concentration. Its mobility, within the plant, is however somewhat constricted by its chemistry and cellular signalling role, and its adsorptive capacity within the aopoplast and the xylem. Supply and demand for Ca is achieved by a homeostatic balance which if perturbed can cause a number of distinctive physiological conditions, often related to Ca deficiency. In this issue Rothwell and Dodd present experiments with bean (Phaseolus vulgaris) and pea (Pisum sativum) plants grown in a field soil exposed to the processes of soil liming (application of Ca carbonate (CaCO₃). Given that there is evidence of free Ca in the xylem sap altering stomatal conductance it is reasonable to ask the question does liming elevate Ca in the transpiration stream which may explain the observed reduced growth which they hypothesise is due to Ca-induced stomatal closure. They show that liming doubled soil exchangeable Ca, reduced stomatal conductance and shoot biomass in both species compared with unlimed controls. However, xylem sap Ca concentration increased only in bean. Interestingly, the same was not true for the pea where the root xylem sap concentration remained unchanged despite an increase in soil available Ca. Given that stomatal conductance decreased in both species, but in response to a lime-induced increase in xylem sap Ca in only one; this questions the role of Ca in inducing stomatal closure. They propose that their data suggest that as yet unidentified antitranspirant causes stomatal closure in both species not the increase in xylem sap Ca per se.     

A thin foot switch

A common problem in determining a number of important gait parameters is a convenient means for indicating foot/floor contact. Various foot switches have been used in many forms, but still an ideal, commercially available switch has yet to materialize. This note describes one method for constructing very thin, (1 mm), durable, switches that have worked well in the Gait Analysis Lab at Texas Scottish Rite Hospital.     

Expansion and cell surface Ig isotype switching in the antigen-binding cell population of nu/nu mice and nu/+ littermates

Swiss-Webster nu/nu splenocytes placed in modified Mishell-Dutton culture containing sheep red blood cells (SRC) generated increased numbers of antigen-binding cells (ABC) compared with antigen-free cultures. In contrast Balb/c nu/nu cultures did not expand their ABC population in response to SRC, suggesting that strain background may influence the effect of the nu/nu gene on T-dependent immune responses. Cell surface Ig isotype analysis indicated that the SRC-induced expanded ABC population exhibited a significant decrease in cell surface IgD and a significant increase in ABC bearing both IgM and IgG. The Swiss-Webster nu/+ littermate cell surface Ig isotype patterns were generally similar to the nu/nu ABC patterns, but with different kinetics.