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Ciliary neuronotrophic factor activates mitogen-activated protein kinase in cultured chick ciliary ganglion neurons.
Neurite outgrowth from embryonic chick ciliary neurons is promoted by ciliary neuronotrophic factor (CNTF), which activates mitogen-activated protein kinase (MAPK). We examined the effect of CNTF on phosphorylation of MAPK in cultured chick ciliary ganglion neurons and immunocytochemical localization of phosphorylated MAPK in the ganglion neurons. Addition of CNTF (50 ng/ml) to the medium increased both [35S]cysteine- and [32P]orthophosphate-labeled MAPK. The CNTF-induced [35S]cysteine-labeled MAPK became phosphorylated within 10 min and the phosphorylated MAPK was dephosphorylated during incubation in CNTF-free medium. In the ganglion neurons, [35S]cysteine-labeled MAPK was mainly localized in the nucleus, while phosphorylated MAPK was localized in both the nucleus and cytoplasm. These results indicate that CNTF activates MAPK in cultured chick ciliary ganglion neurons.The present invention relates to a decoder circuit for use in an electronic apparatus and, more particularly, to a decoder circuit of the type wherein a plurality of data bits from a received bit string are decoded to obtain each bit of decoded data.
An example of the decoder circuit of this type is described in an article entitled "A 10.4 Mb/s DRAM for VLSI" in IEEE Journal of Solid-State Circuits, Vol. SC-18, No. 6, December 1983, pp. 836-844, which is incorporated herein by reference.
The decoder circuit in the article includes an n-bit latch or register in which each of n data bits of received data is stored. To obtain each of n bits of decoded data, the n-bit data bits stored in the n-bit latch are simultaneously compared with the ac619d1d87
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