Sulfate transport through the contraluminal cell membrane of the renal proximal convolution

1982 ◽  
Vol 394 (S1) ◽  
pp. R23-R23
Author(s):  
K. J. Ullrich ◽  
G. Rumrich ◽  
S. Klöss
Keyword(s):  
Cell Membrane ◽  
Sulfate Transport ◽  
Contraluminal Cell Membrane ◽  
Proximal Convolution

scholarly journals Sulfate permeasesphylogenetic diversity of sulfate transport.

2009 ◽  
Vol 56 (3) ◽  
Author(s):  
Sebastian Piłsyk ◽  
Andrzej Paszewski
Keyword(s):  
Cell Membrane ◽  
Posttranslational Modifications ◽  
Subunit Composition ◽  
Transcriptional Level ◽  
Sulfate Assimilation ◽  
Sulfate Transport ◽  
Tight Control ◽  
Sulfate Uptake ◽  
Sulfate Anion ◽  
Evolutionary Origins

Sulfate uptake, the first step of sulfate assimilation in all organisms, is a highly endoergic, ATP requiring process. It is under tight control at the transcriptional level and is additionally modulated by posttranslational modifications, which are not yet fully characterized. Sulfate anion is taken up into the cell by specific transporters, named sulfate permeases, located in the cell membrane. Bacterial sulfate permeases differ significantly from the eukaryotic transporters in their evolutionary origins, structure and subunit composition. This review focuses on the diversity and regulation of sulfate permeases in various groups of organisms.

Active secretion of hypoxanthine and xanthine by guinea pig jejunum in vitro

1980 ◽  
Vol 238 (2) ◽  
pp. G141-G149 ◽  
Author(s):  
N. Kolassa ◽  
W. G. Schutzenberger ◽  
H. Wiener ◽  
K. Turnheim
Keyword(s):  
Cell Membrane ◽  
Guinea Pig ◽  
Enzymic Activity ◽  
Metabolic Energy ◽  
Transepithelial Transport ◽  
Luminal Membrane ◽  
Contraluminal Cell Membrane ◽  
Contraluminal Membrane ◽  
Pig Jejunum

Isolated epithelium of guinea pig jejunum secretes hypoxanthine and xanthine by a transport process that is capable of uphill transport and dependent on metabolic energy supply. Unidirectional influx of hypoxanthine across both the luminal and the contraluminal cell membrane appears to be saturable; influx across the contraluminal membrane is inhibited by 2,4-dinitrophenol (DNP). Efflux across the luminal membrane is diminished by DNP; efflux across the contraluminal membrane is increased by DNP. This evidence suggests the existence of a mediated transport system both in the luminal and the contraluminal cell membrane. Additionally, intracellular metabolism of hypoxanthine seems to regulate transepithelial permeation: increased hypoxanthine salvage by the phosphoribosyltransferase reduces the rate of secretion. However, the incorporation of hypoxanthine into the nucleotides is limited when the hypoxanthine is added to the luminal side of the epithelium, and the permeation rate in the absorptive direction is not markedly influenced by the rate of hypoxanthine salvage. These findings are a further example of the functional orientation of the jejunal epithelial cells with respect to enzymic activity and transepithelial transport properties.

Cytosolic Ca2+ and Na+ activities in perfused proximal tubules of Necturus kidney

1984 ◽  
Vol 247 (1) ◽  
pp. F93-F102 ◽  
Author(s):  
M. Lorenzen ◽  
C. O. Lee ◽  
E. E. Windhager
Keyword(s):  
Cell Membrane ◽  
Epithelial Transport ◽  
Exchange Process ◽  
Cytosolic Calcium ◽  
Ringer Solution ◽  
Proximal Tubules ◽  
Sodium Permeability ◽  
Contraluminal Cell Membrane ◽  
Ion Activity

To study the role of intracellular calcium in the regulation of epithelial transport of ions and water, cytosolic calcium ion activity (aiCa) and cytosolic sodium ion activity (aiNa) were measured in cells of isolated perfused proximal tubules of Necturus kidney. aiCa was measured with Ca2+-selective microelectrodes, aiNa with Na+-selective microelectrodes. Under control conditions, i.e., Ringer solution on both sides of the epithelium, aiCa averaged 71 +/- 7 (SE) nM (n = 21) and aiNa was 12.9 +/- 0.6 mmol (n = 56). When peritubular bath sodium was reduced from 100 to 10 mM by choline substitution, aiCa increased from 73 +/- 14 to 382 +/- 69 nmol (paired t test; P less than 0.001; n = 4); in different tubules, aiNa decreased from 12.8 +/- 1.9 to 8.2 +/- 1.8 mM (P less than 0.001; n = 12). Quinidine (10(-4) M) increased aiCa from 87 +/- 19 to 556 +/- 121 nM (P less than 0.02; n = 5) but reduced aiNa from 15.1 +/- 1.2 to 11.8 +/- 0.8 mM (P less than 0.003; n = 8). In contrast, 10(-4) M ouabain increased both aiCa and aiNa; aiCa rose from 71 +/- 9 to 546 +/- 121 nmol (P less than 0.005; n = 9) and aiNa from 15.1 +/- 1.8 to 70.1 +/- 6.3 mM (P less than 0.001; n = 9). The results are consistent with the existence of a Na-Ca exchange process within the contraluminal cell membrane and with the view that increased aiCa inhibits the tubular transport of sodium by decreasing the sodium permeability of the luminal cell membrane.

Sarcolemmal permeability changes during early myocardial anoxia

1978 ◽  
Vol 36 (2) ◽  
pp. 642-643
Author(s):  
M. Ashraf ◽  
L. Landa ◽  
L. Nimmo ◽  
C. M. Bloor
Keyword(s):  
Cell Membrane ◽  
Membrane Permeability ◽  
Coronary Artery Occlusion ◽  
Artery Occlusion ◽  
Cell Membrane Permeability ◽  
Enzyme Release ◽  
Sprague Dawley ◽  
Sprague Dawley Rats ◽  
Sarcolemmal Permeability ◽  
Membrane Changes

Following coronary artery occlusion, the myocardial cells lose intracellular enzymes that appear in the serum 3 hrs later. By this time the cells in the ischemic zone have already undergone irreversible changes, and the cell membrane permeability is variably altered in the ischemic cells. At certain stages or intervals the cell membrane changes, allowing release of cytoplasmic enzymes. To correlate the changes in cell membrane permeability with the enzyme release, we used colloidal lanthanum (La+++) as a histological permeability marker in the isolated perfused hearts. The hearts removed from sprague-Dawley rats were perfused with standard Krebs-Henseleit medium gassed with 95% O2 + 5% CO2. The hypoxic medium contained mannitol instead of dextrose and was bubbled with 95% N2 + 5% CO2. The final osmolarity of the medium was 295 M osmol, pH 7. 4.

Flagellar Attachment in Selected Trypanosomes

1973 ◽  
Vol 31 ◽  
pp. 496-497
Author(s):  
J. J. Paulin
Keyword(s):  
Cell Membrane ◽  
Lateral Surface ◽  
The Body ◽  
Flagellar Pocket ◽  
Integral Component ◽  
Free Flagellum ◽  
Flagellar Axoneme

Movement in epimastigote and trypomastigote stages of trypanosomes is accomplished by planar sinusoidal beating of the anteriorly directed flagellum and associated undulating membrane. The flagellum emerges from a bottle-shaped depression, the flagellar pocket, opening on the lateral surface of the cell. The limiting cell membrane envelopes not only the body of the trypanosome but is continuous with and insheathes the flagellar axoneme forming the undulating membrane. In some species a paraxial rod parallels the axoneme from its point of emergence at the flagellar pocket and is an integral component of the undulating membrane. A portion of the flagellum may extend beyond the anterior apex of the cell as a free flagellum; the length is variable in different species of trypanosomes.

Trophoblast Cell Membrane Interactions at Implantation

1970 ◽  
Vol 28 ◽  
pp. 310-311
Author(s):  
A. C. Enders
Keyword(s):  
Epithelial Cells ◽  
Cell Membrane ◽  
Membrane Fusion ◽  
Trophoblast Cell ◽  
Membrane Interactions ◽  
Uterine Epithelial Cells ◽  
Functional Complex ◽  
Cytotrophoblast Cells ◽  
Complex Relationships ◽  
Syncytial Trophoblast

The alteration in membrane relationships seen at implantation include 1) interaction between cytotrophoblast cells to form syncytial trophoblast and addition to the syncytium by subsequent fusion of cytotrophoblast cells, 2) formation of a wide variety of functional complex relationships by trophoblast with uterine epithelial cells in the process of invasion of the endometrium, and 3) in the case of the rabbit, fusion of some uterine epithelial cells with the trophoblast.Formation of syncytium is apparently a membrane fusion phenomenon in which rapid confluence of cytoplasm often results in isolation of residual membrane within masses of syncytial trophoblast. Often the last areas of membrane to disappear are those including a desmosome where the cell membranes are apparently held apart from fusion.

Some Conditions Necessary for Pinocytosis

1968 ◽  
Vol 26 ◽  
pp. 142-143
Author(s):  
M. W. Brightman
Keyword(s):  
Smooth Muscle ◽  
Cell Membrane ◽  
Toxic Effects ◽  
Cytological Evidence ◽  
Cell Processes

The cytological evidence for pinocytosis is the focal infolding of the cell membrane to form surface pits that eventually pinch off and move into the cytoplasm. This activity, which can be inhibited by oxidative and glycolytic poisons, is performed only by cell processes that are at least 300A wide. However, the interpretation of such toxic effects becomes equivocal if the membrane invaginations do not normally lead to the formation of migratory vesicles, as in some endothelia and in smooth muscle. The present study is an attempt to set forth some conditions under which pinocytosis, as distinct from the mere inclusion of material in surface invaginations, can take place.

Electron microscopic radioautographic studies on the incorporation of 3H proline in the glomerular basement membrane (GBM) in antistreptococcal-cell-membrane (SCM) injected mice

1984 ◽  
Vol 42 ◽  
pp. 188-189
Author(s):  
R.P. Nayyar ◽  
C.F. Lange ◽  
J. L. Borke
Keyword(s):  
Body Weight ◽  
Cell Membrane ◽  
Basement Membrane ◽  
Glomerular Basement Membrane ◽  
Mesangial Matrix ◽  
Electron Microscopic ◽  
Group A ◽  
Injection Protocol

Streptococcal cell membrane (SCM) antiserum injected mice show a significant thickening of glomerular basement membrane (GBM) and an increase in mesangial matrix within 4 to 24 hours of antiserum administration (1,2,3). This study was undertaken to evaluate the incorporation of 3H proline into glomerular cells and GBM under normal and anti-SCM induced conditions. Mice were administered, intraperitoneally, 0.1 ml of normal or anti-SCM serum followed by a 10 µC/g body weight injection of 3H proline. Details of the preparation of anti-SCM (Group A type 12 streptococcal pyogenes) and other sera and injection protocol have been described elsewhere (2). After 15 minutes of isotope injection a chase of cold proline was given and animal sacrificed at 20 minutes, 1,2,4,8,24 and 48 hours. One of the removed kidneys was processed for immunofluorescence, light and electron microscopic radioautographic studies; second kidney was used for GBM isolation and aminoacid analysis.

High-voltage electron microscopy of patch-clamped membranes

1987 ◽  
Vol 45 ◽  
pp. 582-583
Author(s):  
F. Sachs ◽  
M. J. Song
Keyword(s):  
Electron Microscopy ◽  
Cell Membrane ◽  
Patch Clamp ◽  
High Voltage Electron Microscopy ◽  
Small Patch ◽  
Cellular Electrophysiology ◽  
Voltage Electron ◽  
Electron Microscopes ◽  
Patch Technique ◽  
Membrane Patch

Cellular electrophysiology has been revolutionized by the introduction of patch clamp techniques. The patch clamp records current from a small patch of the cell membrane which has been sucked into a glass pipette. The membrane patch, a few micons in diameter, is attached to the glass by a seal which is electrically, diffusionally and mechanically tight. Because of the tight electrical seal, the noise level is low enough to record the activity of single ion channels over a time scale extending from 10μs to days. However, although the patch technique is over ten years old, the patch structure is unknown. The patch is inside a glass pipette where it has been impossible to see with standard electron microscopes. We show here that at 1 Mev the glass pipette is transparent and the membrane within can be seen with a resolution of about 30 A.

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