Blood–Brain Barrier Protein and Phosphorylation and Dephosphorylation

Capillaries in vertebrate brain have unique permeability properties that make up the blood-brain barrier (BBB). Although it is known that capillaries are innervated by nerve endings of intracerebral origin and that brain capillary function is likely acutely regulated by neuronal inputs, the possible mechanisms of neuronal regulation of capillary function are at present unknown. One possible mode of regulation is via the phosphorylation of brain capillary proteins. The present studies characterize, for the first time, the major phosphoproteins in the bovine brain capillary using both intact bovine brain capillaries and plasma membrane fractions from bovine brain capillaries. The patterns of endogenous phosphorylation of capillary proteins are compared to similar patterns obtained with synaptosomal (P2) fractions from bovine brain. The major findings of this study are: (a) The activity of protein phosphorylation in brain capillaries is localized almost exclusively to the capillary plasma membrane, and is nearly comparable to the activity of protein phosphorylation in synaptosomal membranes. (b) A major phosphoprotein doublet in the capillary fraction comigrates on a sodium dodecyl sulfate gel with a major phosphoprotein doublet of approximate molecular weight of 80K in the synaptosomal fraction, and the latter is presumed to be synapsin I; in dephosphorylation assays the synaptosomal 80K phosphoprotein doublet is not subject to measurable dephosphorylation, whereas the capillary 80K doublet is subject to rapid dephosphorylation, and is essentially completely dephosphorylated within 5 s at 0 degrees C. (c) A prominent triplet of phosphoproteins with molecular weight of 50-55K is present in the capillary fraction, and is not present in the synaptosomal fraction; thus, this 50-55K triplet of phosphoproteins appears specific for brain capillaries.(ABSTRACT TRUNCATED AT 250 WORDS)     

A snapshot of translation in Mycobacterium tuberculosis during exponential growth and nutrient starvation revealed by ribosome profiling

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Marine invasion processes: interactions between native and introduced marsh snails

We test two hypotheses to explain the success of a biological invader in marshes on the Pacific coast of North America. The first hypothesis focuses on the competitive superiority of an invading species over native species; the second hypothesis focuses on the absence of ecological equivalents in the aboriginal biota, such that no competitive interactions are necessary to facilitate successful invasion. As a model system we experimentally manipulated the introduced pulmonate snail Ovatella myosotis and the native prosobranch snails Assiminea californica and Littorina subrotundata. Manipulations included pair-wise enclosures to determine of Ovatella depressed the growth of the native;species; pair-wise associations to determine whether or not snails demonstrated negative or positive clustering; removal experiments to see if native snails invaded regions occupied by Ovatella, and reciprocal transplants on a vertical gradient to determine the physiological breath of the target species. In addition to monitoring population abundances of all three species seasonally, dietary overlap of these gastropods was also examined. No evidence of competitive superiority by Ovatella was found. Ovatella possesses the physiological capacities to exist in a semiterrestrial environment and is therefore able to take advantage of resources unavailable to native gastropods. We conclude that the successful establishment of this Atlantic snail in the Pacific Northwest did not arise at the expense of native species.     

Reduction of Endotoxin Levels in Influenza Virus Vaccines by Barium Sulfate Adsorption-Elution

The level of endotoxin in influenza virus vaccine lots was reduced 10- to 20-fold after barium sulfate adsorption-elution. The amount of viral antigen lost was negligible.     

Is there a relationship between branched amino acid pool size and cell cycle inhibition in roots treated with imidazolinone herbicides?

Excised pea root tips were cultured in White's medium for 24 h and then treated for 12 h with one of the imidazolinone herbicides at 0.2, 2, 20, or 200 μM. Pursuit and Assert were almost ineffective in inhibiting the mitotic index (MI), except at the highest concentrations. Arsenal (ARS) and Scepter both showed good inhibition with 20 μM by 8 h. Adding all three branched amino acids (BAA) (VAL, ILE, and LEU) at 0.1 mM blocked herbicide action. Treatment with the BAAs singly had no protective effect. Experiments were performed to determine the BAA pool size and MI after an 8-h treatment with ARS at 2 and 200 μM and Chlorsulfuron (CS), a sulfonylurea herbicide, at 28 nM. Both CS and ARS at 200 μM inhibited the MI to almost 0 by 8 h. ARS at 2 μM inhibited the MI by about 40%. The BAA pool size in all three treatments was reduced by approximately 50%, whether the MI was totally blocked or not. The 1-mm root tips had a greater amount of VAL than did the mature portions of the roots, whereas ILE and LEU were slightly less in the root tip. Other soluble amino acids did not show consistent differences between herbicide-treated roots and controls. The implications of the pool size reduction, in instances where the MI was not totally inhibited, is discussed in light of new data from other laboratories on the mode of action of the imidazolinone herbicides.