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Biomedical subjects

J Jones

Publications and source records attributed to J Jones.

At least 757 records · Page 42Linked to original sources

Separation of cells having histochemically demonstrable glucose-6-phosphatase from suspensions of hamster kidney cells in an isokinetic density gradient of Ficoll in tissue culture medium.

Suspensions of enzymatically disaggregated hamster kidney cells were separated primarily according to differences in diameter using velocity sedimentation in a previously described isokinetic density gradient and according to differences in density in an isopycnic density gradient. Cells which contained histochemically demonstrable glucose-6-phosphatase were thought to be cells from proximal tubules and constituted 46.5 +/- 14.1% of the cells in the starting sample suspension of disaggregated kidney cells. The purest gradient fractions from experiments using velocity sedimentation contained 98.0 +/- 0.6% cells which demonstrated glucose-6-phosphatase activity. More than 99.0% of these cells excluded trypan blue. Isopycnic sedimentation was not an effective means of purifying proximal tubule cells.

Animals↗

Separation of acinar cells from lactating mammary gland using velocity sedimentation in an isokinetic gradient of Ficoll in tissue culture medium.

This report describes a procedure for the purification of acinar cells from the disaggregated lactating mammary gland of the rat. Following disaggregation of the 15 days postpartum mammary gland, two qualitatively different kinds of cells which exhibited alkaline phosphatase activity were identified. These two populations of cells were separated in a previously described isokinetic gradient of Ficoll in tissue culture medium using a centrifugal force of 55g for 14 minutes. The larger of these two types of cells was found in a well-defined subpopulation of mammary cells, 97.4 +/- 0.8% of which lacked demonstrable adenosine triphosphatase activity by light microscopy. Ultrastructurally, these cells were identified as being almost exclusively acinar cells. The potential significance of this method is discussed.

Alkaline Phosphatase↗

Coeliac disease.

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Adult↗

Lung surface-active fraction as a model system for macromolecular ultrastructural studies with Crotalus atrox venom.

The dog lung surface-active fraction and phosphatidylcholine constituents were subjected to hydrolysis by Crotalus atrox phospholipase A(2). Relative rates of hydrolysis were: dipalmitoyl glycerophosphorylcholine > phosphatidylcholine isolated from the surface-active fraction > phosphatidylcholine as an integral component of the intact surface-active macromolecular structure. Cholesterol markedly inhibited, whereas tripalmitin increased, the rate of hydrolysis with both pure phosphatidylcholine substrates. The effect of temperature on the velocity indicated the enzyme was most active when the substrates were in the gel state. These kinetic results, in conjunction with surface chemistry studies, can be interpreted to indicate that the phosphatidylcholine in the intact surface-active macromolecular particle is liquid crystalline due to molecular interactions with other constituents. Gas-liquid chromatographic analysis of the 2-lysophosphatidylcholines and fatty acids produced from the enzymatic hydrolysis of the intact surface-active fraction indicated that palmitoyl residues were more accessible to the enzyme, perhaps because they occupied positions near the surface of the particle.

Animals↗

Slaves of the lamp.

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Family Characteristics↗