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W Chou

Publications and source records attributed to W Chou.

27 records · Page 2Linked to original sources

Development of spontaneous electrical activity by rat hypothalamic neurons in dissociated culture.

The development of spontaneous electrical activity by embryonic rat hypothalamic neurons in dissociated culture was monitored using an extracellular, patch electrode recording method. Embryonic day 17 hypothalamic neurons were plated onto a feeder layer of astrocytes obtained from neonatal rat cerebral cortex, and extracellular electrical activity was monitored beginning the day after plating. The rates and patterns of spontaneous discharge were examined using interpike interval histograms. The percentage of spontaneously active neurons increased steadily with time in culture, from 13% in the first week to 56% during the sixth week in vitro. Although the percentage of spontaneously active cells increased, average firing rates did not change with time in culture. The pattern of electrical discharge was primarily random at all time points, with a small number of cells displaying regular activity while 4 cells were classified as phasic/bursty. In general, spontaneous action potential discharge was not dependent on synaptic transmission, as activity persisted after perfusion with bath solution containing either low Ca2+/high Mg2+ or kynurenic acid. Tetrodotoxin consistently and reversibly abolished spontaneous firing, regardless of culture age. We conclude that spontaneous activity in low density hypothalamic culture develops gradually though steadily, and is generated through an endogenous mechanism, independent of synaptic excitation.

Action Potentials↗

Phosphorylation downregulates the DNA-binding activity of simian virus 40 T antigen.

Proteolytic fragments of simian virus 40 tumor (T) antigen and T antigen that was dephosphorylated with alkaline phosphatase bound between 1.5 to 2 times more origin-containing simian virus 40 DNA than did intact T antigen in DNA saturation experiments. Kinetic experiments showed that these treatments also enhanced the rate at which T antigen bound to the DNA. The enhanced binding of T-antigen fragments correlated with the generation of DNA-binding fragments that lacked the NH2-terminal region. Dephosphorylation of T antigen in vitro resulted in the removal of phosphate groups from the NH2-terminal region as well as from the COOH-terminal region. To test the effects of dephosphorylation on the size of the protein, immunoaffinity-purified T antigen was subjected to sedimentation with and without prior treatment with alkaline phosphatase. Most of the purified protein sedimented as a monomer and no significant effect was observed after dephosphorylation, indicating that the enhanced DNA-binding activity was probably not due to the uncovering of additional binding sites buried specifically in oligomerized T antigen. Taken together, these results indicate that in vivo phosphorylation of the NH2-terminal region (residues 106 to 124) decreases the binding of the protein to the DNA origin. The effect is reversed by in vitro dephosphorylation or by proteolysis which removes the highly phosphorylated NH2-terminal arm of the polypeptide. We suggest that phosphorylation inactivates one of two distinct DNA-binding activities on the polypeptide chain perhaps corresponding to two separate regions in T antigen.

Antigens, Viral, Tumor↗