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J Ting

Publications and source records attributed to J Ting.

24 records · Page 2Linked to original sources
PubMed1987

Interleukin 2 responses of lpr and normal L3T4-/Lyt-2- T cells induced by TPA plus A23187.

The major population of cells that accumulate abnormally in MRL/Mp-lpr/lpr lymphoid tissue is Thy-1+, L3T4-, and Lyt-2-. To clarify the functional potential of these cells, we examined their proliferation, interleukin 2 (IL 2) receptor expression, and IL 2 secretion by using as stimulants the combination of 12-O-tetradecanoylphorbol-2-acetate and A23187 (a calcium ionophore). Although the lpr T cells were capable of responding to these stimulants, the nature of the response and of the concentrations of ligand required differed sharply from the responses of normal adult T cells, and of adult L3T4-Lyt-2- thymocytes. There was a strong similarity but not identity when responses of 16 day fetal thymocytes were compared with those of lpr L3T4-Lyt-2- cells. The unusual functional properties of the lpr cells, such as high A23187 dose requirement for maximal proliferation, low percentage of IL 2 receptor-expressing cells, and low levels of IL 2 secretion, suggested that these cells are arrested at a stage of development similar to that of 16-day fetal thymocytes and before adult L3T4-/Lyt-2- thymocytes.

Animals↗
PubMed1987

The nucleotide sequence encoding the hamster 78-kDa glucose-regulated protein (GRP78) and its conservation between hamster and rat.

The complete nucleotide (nt) sequence encoding the hamster 78-kDa glucose-regulated protein has been determined using a cDNA plasmid p3C5. Comparison of the nucleotide sequences from rat and hamster showed a strong conservation in the coding region as well as 5'- and 3'-untranslated regions (UTRs). The relatively long (206 nt for rat) 5'UTR shares 72% sequence homology between rat and hamster in the 142 nt upstream from the ATG start codon. This conserved region contained an imperfect inverted-repeat sequence. The long 5'UTR region is capable of forming stable dyad structures. The homology within the rat and hamster protein-coding region is 93.7%, with most of the differences resulting in silent site mutations. Out of the 654 amino acids, only four changes are detected, two of which are located in the signal peptide. While the sizes of the 3'UTR are different between the two species compared, strong sequence homologies (95%) were observed throughout the entire UTRs. Also, the 3'UTR was not rich in A + T residues as found in other eukaryotic mRNAs.

Animals↗
PubMed1986

Calcium ionophore A23187 as a regulator of gene expression in mammalian cells.

The calcium ionophore A23187 can reversibly induce the expression of two glucose-regulated genes, p3C5 and p4A3. This induction requires a continuous presence of the ionophore for over 2 h. Although extracellular Ca2+ is important for the optimal effect of A23187, it is not necessary for the induction, since a similar response with a lower magnitude can be triggered in cells cultured in low Ca2+ medium buffered with EGTA. Both the basal and induced levels of p3C5 and p4A3 transcripts can be modulated by the calmodulin antagonist W-7, indicating the involvement of Ca2+/calmodulin-associated pathways. In addition, the sensitivity of the A23187 induction to cycloheximide suggests that the induction process is dependent on de novo protein synthesis.

Animals↗
PubMed1984

Biochemical characterization of the 94- and 78-kilodalton glucose-regulated proteins in hamster fibroblasts.

This report concerns further characterization of the 94-kDa and the 78-kDA glucose-regulated proteins which are the major proteins overproduced in hamster fibroblasts when the cells are starved of glucose. Using a temperature-sensitive mutant, K12, which synthesizes high levels of these proteins at the nonpermissive temperature, we purified both proteins by two-dimensional gel electrophoresis and determined their amino acid compositions as well as the NH2-terminal sequences. Both proteins contain an unusual NH2-terminal sequence rich in glutamic and aspartic acid residues. Biochemical fractionation of these proteins demonstrated that the 78-kDa glucose-regulated protein is present in the nuclear fraction. In addition, we show that phosphate incorporation into the 78-kDa protein is specifically affected in the K12 mutant cells.

Amino Acid Sequence↗
PubMedDate not supplied

A simple method of producing depth ionization data for electron energy constancy check.

A simple method has been developed to reproduce depth ionization data of electron beams for energy determination. The method utilizes a simple set of equipment, a combination of a specially designed wedge-shaped polystyrene phantom and a linear array of detectors, to collect the necessary data. The wedge-shaped phantom provides varying depths to various detectors in the array. The ionization readings received from the detectors were corrected for off-axis ratio and plotted against corresponding ray-line depths to produce depth ionization curves. The instrument setup was fast and simple. The relevant data, for a high-energy linear accelerator with multiple electron energies, were collected in minutes. The depths of 80% and 50% ionization determined by this method were found to differ by 2 and 3 mm, respectively, at the most, with those determined by a conventional method.

Biophysical Phenomena↗