Literature DB >> 2254448

Electrophysiological identification of alpha- and beta-intercalated cells and their distribution along the rabbit distal nephron segments.

S Muto1, K Yasoshima, K Yoshitomi, M Imai, Y Asano.   

Abstract

By cable analysis and intracellular microelectrode impalement in the in vitro perfused renal tubule, we identified alpha- and beta-intercalated (IC) cells along the rabbit distal nephron segments, including the connecting tubule (CNT), the cortical collecting duct (CCD), and the outer medullary collecting duct in the inner stripe (OMCDi). IC cells were distinguished from collecting duct (CD) cells by a relatively low basolateral membrane potential (VB), a higher fractional apical membrane resistance, and apparent high Cl- conductances of the basolateral membrane. Two functionally different subtypes of IC cells in the CCD were identified based on different responses of VB upon reduction of the perfusate Cl- from 120 to 12 mM: the basolateral membrane of beta-IC cells was hyperpolarized, whereas that of alpha-IC cells was unchanged. This is in accord with the hypothesis that the apical membrane of beta-IC cells contains some Cl(-)-dependent entry processes, possibly a Cl-/HCO3- exchanger. Further characterization of electrical properties of both subtypes of IC cells were performed upon lowering bath or perfusate Cl- from 120 to 12 mM, and raising bath or perfusate K+ from 5 to 50 mM. A 10-fold increase in the perfusate K+ had no effect on VB in both subtypes of IC cells. Upon abrupt changes in Cl- or K+ concentration in the bath, a large or a small depolarization of the basolateral membrane, respectively, was observed in both subtypes of IC cells. The electrical properties of alpha- and beta-IC cells were similar among the distal nephron segments, but their distribution was different: in the CNT, which consists of IC cells and CNT cells, 97.3% (36/37) of IC cells were of the beta type. In the CCD, which consists of IC cells and CD cells, 79.8% (79/99) of IC cells were of the beta-type, whereas in the OMCDi 100% (19/19) were of the alpha type, suggesting that the beta type predominates in the earlier and the alpha type in the later segment.

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Year:  1990        PMID: 2254448      PMCID: PMC329815          DOI: 10.1172/JCI114913

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  47 in total

1.  Effect of vasopressin on electrical resistance of renal cortical collecting tubules.

Authors:  S I Helman; J J Grantham; M B Burg
Journal:  Am J Physiol       Date:  1971-06

2.  Microelectrode assessment of chloride-conductive properties of cortical collecting duct.

Authors:  S C Sansom; E J Weinman; R G O'Neil
Journal:  Am J Physiol       Date:  1984-08

3.  Model of active transepithelial Na and K transport of renal collecting tubules.

Authors:  S I Helman; R G O'Neil
Journal:  Am J Physiol       Date:  1977-12

4.  Transport characteristics of renal collecting tubules: influences of DOCA and diet.

Authors:  R G O'Neil; S I Helman
Journal:  Am J Physiol       Date:  1977-12

5.  Preparation and study of fragments of single rabbit nephrons.

Authors:  M Burg; J Grantham; M Abramow; J Orloff
Journal:  Am J Physiol       Date:  1966-06

6.  Internephron heterogeneity for carbonic anhydrase-independent bicarbonate reabsorption in the rat.

Authors:  J P Frommer; M E Laski; D E Wesson; N A Kurtzman
Journal:  J Clin Invest       Date:  1984-04       Impact factor: 14.808

7.  Bicarbonate absorption by rabbit cortical collecting tubules in vitro.

Authors:  T D McKinney; M B Burg
Journal:  Am J Physiol       Date:  1978-02

8.  Mineralocorticoid modulation of rabbit medullary collecting duct acidification. A sodium-independent effect.

Authors:  D K Stone; D W Seldin; J P Kokko; H R Jacobson
Journal:  J Clin Invest       Date:  1983-07       Impact factor: 14.808

9.  Bicarbonate transport in cortical and outer medullary collecting tubules.

Authors:  W E Lombard; J P Kokko; H R Jacobson
Journal:  Am J Physiol       Date:  1983-03

10.  Characterization of acidification in the cortical and medullary collecting tubule of the rabbit.

Authors:  M E Laski; N A Kurtzman
Journal:  J Clin Invest       Date:  1983-12       Impact factor: 14.808

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  35 in total

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Journal:  Compr Physiol       Date:  2015-01       Impact factor: 9.090

Review 6.  Molecular mechanisms and regulation of urinary acidification.

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7.  Electrical properties of the rabbit cortical collecting duct from obstructed kidneys after unilateral ureteral obstruction. Effects of renal decapsulation.

Authors:  S Muto; Y Asano
Journal:  J Clin Invest       Date:  1994-11       Impact factor: 14.808

8.  Effect of prostaglandin E2 on agonist-stimulated cAMP accumulation in the distal convoluted tubule isolated from the rabbit kidney.

Authors:  N M Griffiths; C Brick-Ghannam; S Siaume-Perez; D Chabardès
Journal:  Pflugers Arch       Date:  1993-03       Impact factor: 3.657

9.  Inhibition of amiloride-sensitive apical Na+ conductance by acetylcholine in rabbit cortical collecting duct perfused in vitro.

Authors:  M Takeda; K Yoshitomi; J Taniguchi; M Imai
Journal:  J Clin Invest       Date:  1994-06       Impact factor: 14.808

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Journal:  J Vet Sci       Date:  2007-12       Impact factor: 1.672

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