Evidence map›Paper›PMID 1608958›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1992

Differentiation of renal beta-intercalated cells to alpha-intercalated and principal cells in culture.

G Fejes-Tóth, A Náray-Fejes-Tóth

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.7field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 95 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Acidosis induces antimicrobial peptide expression and resistance to uropathogenicAmerican journal of physiology. Renal physiology · 2020
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Development of the Mammalian Kidney.Current topics in developmental biology · 2016
    Review
  18. Article
  19. Adam10 mediates the choice between principal cells and intercalated cells in the kidney.Journal of the American Society of Nephrology : JASN · 2015
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

G Fejes-TóthDepartment of Physiology, Dartmouth Medical School, Hanover, NH 03756.
A Náray-Fejes-Tóth
Dartmouth College · US

Funding

CORTICOSTEROID INTERACTIONS IN ION TRANSPORTR01DK041841 · NIDDK · HENRY FORD HOSPITAL · PI NARAY-FEJES-TOTH, ANIKO · 1989 to 2009
$2.7M
ISOLATED COLLECTING TUBULE CELLS--ION TRANSPORTR01DK039523 · NIDDK · HENRY FORD HOSPITAL · PI FEJES-TOTH, GEZA · 1989 to 1998
–
NIDDK NIH HHS DK-39523NIDDK NIH HHS DK-41841
6 · The paper itself

Abstract

The renal collecting duct is a heterogenous epithelium consisting of intercalated cells (ICC) and principal cells (PC). The origin of this cellular heterogeneity is not clear. To test the hypothesis that the two cell types might originate from one another, pure populations of ICC (beta subtype) and PC were isolated by fluorescence-activated cell sorting and grown on permeable supports. After the monolayers reached confluence, the expression of ICC- and PC-specific functions and antigens was monitored. Cultures of sorted beta-ICC, in addition to expressing ICC-specific functions (such as an electrogenic H+ secretion) and antigens, progressively acquired PC functions (amiloride-sensitive Na+ transport and K+ secretion). On day 6, cultures of sorted beta-ICC exhibited a lumen-negative transepithelial potential difference of 83 +/- 4 mV and a short circuit current of 107 +/- 15 microA/cm2 and created a lumen-to-bath K+ concentration ratio of approximately 10. The percentage of cells staining with two PC-specific antibodies was 53% and 65%. On the other hand, cultures of sorted PC failed to acquire ICC-specific functions while maintaining PC characteristics. To rule out preferential proliferation of a few contaminating PC as an explanation of these results, we have generated a continuous collecting duct cell line (M-1) originating from mice transgenic for the early region of simian virus 40. Cell lines cloned from M-1 cells exhibit both PC and ICC functions and show mutually exclusive heterogenous expression of PC and ICC antigens, demonstrating a common origin of the two cell types. These data indicate that while beta-ICC in culture can give rise to both alpha-ICC and PC, PC cannot convert to ICC, which raises the possibility that beta-ICC is the stem cell in the renal collecting duct. Differentiation of ICC to PC may explain the cellular heterogeneity in the cortical collecting duct.

Indexed as

AcetazolamideAnimalsAntibodies, MonoclonalCell DifferentiationCells, CulturedCell SeparationClone CellsEpithelial CellsEpitheliumFlow CytometryFluorescein-5-isothiocyanateHydrogen-Ion ConcentrationKidney Tubules, CollectingMammalsMembrane PotentialsPotassiumAcetazolamideAntibodies, MonoclonalFluorescein-5-isothiocyanatePotassiumSodium

Identifiers

PMID1608958
PMCPMC49317
OpenAlexW2076028855

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.