Impairment in S-phase entry of splenocytes of Parp-1 knockout mice

One immediate cellular response to DNA damage is the polyADP-ribosylation reaction by poly(ADP-ribose) polymerase-1 (Parp-1). The importance of Parp-1 has been established in many cellular processes, such as the maintenance of genomic stability, DNA repair and cell-death induction. Here, we established Parp-1^−/− mice of C57BL/6J congenic strain and characterized the role of Parp-1 in cell-cycle progression. In this study, we also improved a method to observe G0/G1 to S-phase transition of splenocytes and bone marrow cells prepared from mice. The cells were cultured and stimulated with mitogens (50 μM ionomycin/1 μM phorbol 12, 13-dibutyrate). We found that addition of a commercially available growth supportive reagent, BM Condimed ^RH1, greatly enhanced the transition of G0/G1 to the S-phase, which was determined by bromodeoxyuridine (BrdU) incorporation to DNA. Using this method, G0/G1 to the S-phase entry was measured using splenocytes derived from Parp-1^−/−, Parp-1^+/− and wild-type (Parp-1^+/+) mice. DNA synthesis in Parp-1^+/+ and Parp-1^+/− splenocytes started from day 1 after addition of mitogens, whereas that in Parp-1^−/− cells started from day 2. The peak of the S-phase was at day 2 in all genotypes and notably DNA synthesis in Parp-1^−/− cells was approximately halved compared to Parp-1^+/+ cells on day 2, 3 and 4. These results suggested that Parp-1 is involved in positive regulation of S-phase entry in quiescent mouse splenocytes.     

Polymerization of vinyl compounds in the presence of perfluoroisopropenyl ester

To report a new polymerization reaction phenomenon, this article examines the polymerization of butyl vinyl ether and N‐vinylcarbazole in the presence of 2‐benzoxypentafluoropropene [CF₂?C(CF₃)OCOC₆H₅ or BPFP]. The homopolymer of butyl vinyl ether was produced in the presence of a catalytic amount of BPFP in high yields. N‐Vinylcarbazole, which is a monomer well‐known for producing its homopolymer under cationic polymerization conditions, also yielded its homopolymer in the presence of BPFP. It was concluded that some cationic species would be yielded by the addition of BPFP. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 908–910, 2007.     

Electronic specific heat for the Anderson model

The expression of the electronic specific heat for the symmetric Anderson model is obtained in closed form.     

Phase unwrapping method along radial coordinates for speckle image reconstruction

We describe a phase estimating technique for a stellar speckle image reconstruction, which is based on the phase unwrapping method in polar coordinates. The phase unwrapping along radial lines is favorable to reduce accumulating errors in the phase estimation. This method is combined with Bruck-Sodin method which gives the estimate of the modulus of an object transform without a point reference source. Computer simulations of the image reconstruction are presented.     

Negative theta-pinch experiment

Plasma temperature obtained with a negative theta-pinch experiment is somewhat lower than that with an ordinary thete-pinch. This is consistent with a numerical calculation assuming Sagdeev resistivity.     

Quantal master equation valid for any time scale

A new memoryless expression for the equation of motion for the reduced density matrix is derived. It is equivalent to that proposed by Tokuyama and Mori, but has a more convenient form for the application of the perturbational expansion method. The master equation derived from this form of equation in the first Born approximation is applied to two examples, the Brownian motion of a quantal oscillator and that of a spin. In both examples the master equation is rewritten into the coherent-state representation. A comparison is made with the stochastic theory of the spectral line shape given by Kubo, and it is shown that this theory of the line shape can be incorporated into the framework of the present theory.     

Alkynes as activators in the nickel-catalysed addition of organoboronates to aldehydes

Alkynes act not as substrates but as co-catalysts in the presence of a nickel catalyst, an organoboronate and an aldehyde to promote the addition reaction between the substrates in combination with H2O.