Literature DB >> 3421894

Study of the mechanism by which the Na+-Pi co-transporter of mouse kidney proximal-tubule cells adjusts to phosphate depletion.

M Jahan1, P J Butterworth.   

Abstract

1. Proximal-tubule cells isolated from mouse kidney after digestion with collagenase take up Pi by an Na+-dependent and saturable process mediated by the Na+-Pi co-transporter of the brush-border membrane. 2. Pi depletion of the cells is accompanied by a stimulation of Pi-transport activity. Kinetic investigations reveal that Vmax. is increased by 90% and Km decreased by 50% after Pi depletion. Transport activity returns to normal values after incubation for 30 min at 37 degrees C of Pi-depleted cells in normal medium containing 1 mM-Pi, but the fall in transport activity under these conditions is inhibited by colchicine. 3. The energy of activation of Na+-Pi co-transport activity of depleted cells differs greatly from that found for normal replete cells. 4. The results provide evidence that stimulation of transport by Pi depletion arises from an increase in the number of carrier sites in the brush-border membrane. Additionally, changes in the properties of the transporter occur which may reflect altered phospholipid-carrier-protein interaction in the Pi-depleted condition.

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Year:  1988        PMID: 3421894      PMCID: PMC1149112          DOI: 10.1042/bj2520105

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  15 in total

1.  Hexikinase of rat brain.

Authors:  A C Chou; J E Wilson
Journal:  Methods Enzymol       Date:  1975       Impact factor: 1.600

Review 2.  Cellular mechanisms of inorganic phosphate transport in kidney.

Authors:  P Gmaj; H Murer
Journal:  Physiol Rev       Date:  1986-01       Impact factor: 37.312

3.  Reconstitution of the partially purified renal phosphate (Pi) transporter.

Authors:  C Schäli; D A Vaughn; D D Fanestil
Journal:  Biochem J       Date:  1986-04-01       Impact factor: 3.857

Review 4.  Renal handling of phosphate and calcium.

Authors:  V W Dennis; W W Stead; J L Myers
Journal:  Annu Rev Physiol       Date:  1979       Impact factor: 19.318

Review 5.  The statistical analysis of enzyme kinetic data.

Authors:  W W Cleland
Journal:  Adv Enzymol Relat Areas Mol Biol       Date:  1967

6.  Adaptation of phosphate transport in phosphate-deprived LLC-PK1 cells.

Authors:  J Caverzasio; C D Brown; J Biber; J P Bonjour; H Murer
Journal:  Am J Physiol       Date:  1985-01

7.  Influence of temperature on phosphate uptake by renal brush border membrane vesicles.

Authors:  M G Brunette; R Béliveau
Journal:  Adv Exp Med Biol       Date:  1984       Impact factor: 2.622

8.  The interaction between gluconeogenic metabolism and accumulation of phosphate by chick kidney tubule cells.

Authors:  M F Grahn; R Parveen; P J Butterworth
Journal:  Cell Biochem Funct       Date:  1985-07       Impact factor: 3.685

9.  Membrane fluidity and enzyme activities in brush border and basolateral membranes of the dog kidney.

Authors:  C Le Grimellec; M C Giocondi; B Carrière; S Carrière; J Cardinal
Journal:  Am J Physiol       Date:  1982-03

10.  Mechanism of rapid phosphate (Pi) transport adaptation to a single low Pi meal in rat renal brush border membrane.

Authors:  J Caverzasio; J P Bonjour
Journal:  Pflugers Arch       Date:  1985-07       Impact factor: 3.657

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  3 in total

1.  Functional asymmetry of phosphate transport and its regulation in opossum kidney cells: phosphate "adaptation".

Authors:  S J Reshkin; J Forgo; J Biber; H Murer
Journal:  Pflugers Arch       Date:  1991-10       Impact factor: 3.657

2.  32P-labelling anomalies in human erythrocytes. Is there more than one pool of cellular Pi?

Authors:  G J Kemp; A Bevington; D Khodja; A Challa; R G Russell
Journal:  Biochem J       Date:  1989-12-15       Impact factor: 3.857

Review 3.  Hyperphosphatemia Management in Patients with Chronic Kidney Disease.

Authors:  Ahmed M Shaman; Stefan R Kowalski
Journal:  Saudi Pharm J       Date:  2015-01-12       Impact factor: 4.330

  3 in total

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