Evidence map›Paper›PMID 20719981›Full record

ArticleAmerican journal of physiology. Renal physiology2010

Direct demonstration of tubular fluid flow sensing by macula densa cells.

Arnold Sipos, Sarah Vargas, János Peti-Peterdi

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.5field-weighted citation impact, top 15% 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

27 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. A new view of macula densa cell protein synthesis.American journal of physiology. Renal physiology · 2021
    Article
  4. A new view of macula densa cell microanatomy.American journal of physiology. Renal physiology · 2021
    Article
  5. Salt intake and the dance of the macula densa cells.American journal of physiology. Renal physiology · 2021
    Article
  6. Review
  7. Review
  8. Article
  9. TRPV4 deletion protects against hypokalemia during systemic KAmerican journal of physiology. Renal physiology · 2019
    Article
  10. "I don't get no respect": the role of chloride in acute kidney injury.American journal of physiology. Renal physiology · 2019
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Shear stress blunts tubuloglomerular feedback partially mediated by primary cilia and nitric oxide at the macula densa.American journal of physiology. Regulatory, integrative and comparative physiology · 2015
    Article
  18. Newly stemming functions of macula densa-derived prostanoids.Hypertension (Dallas, Tex. : 1979) · 2015
    Article
  19. Renal autoregulation in health and disease.Physiological reviews · 2015
    Review
  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

3 authors at 2 institutions in 2 countries.

Arnold SiposZilkha Neurogenetic Institute, ZNI335, Univ. of Southern California, 1501 San Pablo St., Los Angeles, CA 90033, USA.
Sarah Vargas
János Peti-Peterdi
Hungarian Academy of Sciences · HUUniversity of Southern California · US

Funding

Multiphoton Imaging of the Juxtaglomerular ApparatusR01DK064324 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JANOS PETI-PETERDI · 2004 to 2026
$8.4M
NIDDK NIH HHS DK-064324NIDDK NIH HHS R01 DK064324
6 · The paper itself

Abstract

Macula densa (MD) cells in the cortical thick ascending limb (cTAL) detect variations in tubular fluid composition and transmit signals to the afferent arteriole (AA) that control glomerular filtration rate [tubuloglomerular feedback (TGF)]. Increases in tubular salt at the MD that normally parallel elevations in tubular fluid flow rate are well accepted as the trigger of TGF. The present study aimed to test whether MD cells can detect variations in tubular fluid flow rate per se. Calcium imaging of the in vitro microperfused isolated JGA-glomerulus complex dissected from mice was performed using fluo-4 and fluorescence microscopy. Increasing cTAL flow from 2 to 20 nl/min (80 mM [NaCl]) rapidly produced significant elevations in cytosolic Ca(2+) concentration ([Ca(2+)](i)) in AA smooth muscle cells [evidenced by changes in fluo-4 intensity (F); F/F(0) = 1.45 ± 0.11] and AA vasoconstriction. Complete removal of the cTAL around the MD plaque and application of laminar flow through a perfusion pipette directly to the MD apical surface essentially produced the same results even when low (10 mM) or zero NaCl solutions were used. Acetylated α-tubulin immunohistochemistry identified the presence of primary cilia in mouse MD cells. Under no flow conditions, bending MD cilia directly with a micropipette rapidly caused significant [Ca(2+)](i) elevations in AA smooth muscle cells (fluo-4 F/F(0): 1.60 ± 0.12) and vasoconstriction. P2 receptor blockade with suramin significantly reduced the flow-induced TGF, whereas scavenging superoxide with tempol did not. In conclusion, MD cells are equipped with a tubular flow-sensing mechanism that may contribute to MD cell function and TGF.

Indexed as

Aniline CompoundsAnimalsBody FluidsCiliaFluorescent DyesImmunohistochemistryIn Vitro TechniquesJuxtaglomerular ApparatusKidney CortexKidney GlomerulusKidney TubulesMechanoreceptorsMiceMice, Inbred C57BLNephronsPerfusionAniline CompoundsFluo 4Fluorescent DyesSodium ChlorideXanthenes

Identifiers

PMID20719981
PMCPMC2980403
OpenAlexW2169230483

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.