Evidence map›Paper›PMID 23148317›Full record

ArticleThe Journal of physiology2013

Functional expression of SK channels in murine detrusor PDGFR+ cells.

Haeyeong Lee, Byoung H Koh, Lauren E Peri, Kenton M Sanders, Sang Don Koh

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

43 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Regulation of PDGFRαHeliyon · 2024
    Article
  6. Defining the molecular fingerprint of bladder and kidney fibroblasts.American journal of physiology. Renal physiology · 2023
    Review
  7. Article
  8. Cardiac PDGFRαFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  9. Vascular mechanotransduction.Physiological reviews · 2023
    Review
  10. Article
  11. Article
  12. Role of detrusor PDGFRαScientific reports · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. 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

5 authors at 1 institution in 1 country.

Haeyeong LeeDepartment of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV 89557, USA.
Byoung H Koh
Lauren E Peri
Kenton M Sanders
Sang Don Koh
University of Nevada, Reno · US

Funding

Tissue, Cell and Tissue Culture CoreP01DK041315 · NIDDK · UNIVERSITY OF NEVADA RENO · PI KEEF, KATHLEEN D · 1989 to 2018
$26.3M
STRETCH DEPENDENT POTASSIUM CHANNEL REGULATION IN OVERACTIVE BLADDERP20RR018751 · NCRR · UNIVERSITY OF NEVADA RENO · PI RO, SEUNGIL · 2003 to 2011
$17.3M
Molecular and Functional Mechanisms of Purinergic Relaxation in Detrusor MuscleR01DK098388 · NIDDK · UNIVERSITY OF NEVADA RENO · PI KOH, SANG DON · 2013 to 2017
$1.6M
Zeiss LSM 510 Laser Scanning Confocal MicroscopeS10RR016871 · NCRR · UNIVERSITY OF NEVADA RENO · PI WARD, SEAN M · 2002 to 2002
$453k
NCRR NIH HHS 1 S10 RR16871NCRR NIH HHS P20 RR018751NCRR NIH HHS P20-RR18751NIDDK NIH HHS P01 DK041315NIDDK NIH HHS P01 DK41315NIDDK NIH HHS R01 DK098388
6 · The paper itself

Abstract

We sought to characterize molecular expression and ionic conductances in a novel population of interstitial cells (PDGFRα(+) cells) in murine bladder to determine how these cells might participate in regulation of detrusor excitability. PDGFRα(+) cells and smooth muscle cells (SMCs) were isolated from detrusor muscles of PDGFRα(+)/eGFP and smMHC/Cre/eGFP mice and sorted by FACS. PDGFRα(+) cells were highly enriched in Pdgfra (12 fold vs. unsorted cell) and minimally positive for Mhc (SMC marker), Kit (ICC marker) and Pgp9.5 (neuronal marker). SK3 was dominantly expressed in PDGFRα(+) cells in comparison to SMCs. αSlo (BK marker) was more highly expressed in SMCs. SK3 protein was observed in PDGFRα(+) cells by immunohistochemistry but could not be resolved in SMCs. Depolarization evoked voltage-dependent Ca(2+) currents in SMCs, but inward current conductances were not activated in PDGFRα(+) cells under the same conditions. PDGFRα(+) cells displayed spontaneous transient outward currents (STOCs) at potentials positive to -60 mV that were inhibited by apamin. SK channel modulators, CyPPA and SKA-31, induced significant hyperpolarization of PDGFRα(+) cells and activated SK currents under voltage clamp. Similar responses were not resolved in SMCs at physiological potentials. Single channel measurements confirmed the presence of functional SK3 channels (i.e. single channel conductance of 10 pS and sensitivity to intracellular Ca(2+)) in PDGFRα(+) cells. The apamin-sensitive stabilizing factor regulating detrusor excitability is likely to be due to the expression of SK3 channels in PDGFRα(+) cells because SK agonists failed to elicit resolvable currents and hyperpolarization in SMCs at physiological potentials.

Indexed as

Action PotentialsAnimalsApaminBenzothiazolesCalciumGene ExpressionInterstitial Cells of CajalMiceMice, Inbred C57BLMyocytes, Smooth MusclePotassiumPotassium Channel BlockersPyrazolesPyrimidinesReceptor, Platelet-Derived Growth Factor alphaSmall-Conductance Calcium-Activated Potassium ChannelsApaminBenzothiazolesCalciumcyclohexyl-(2-(3,5-dimethylpyrazol-1-yl)-6-methylpyrimidin-4-yl)aminenaphtho(1,2-d)thiazol-2-ylaminePotassiumPotassium Channel BlockersPyrazolesPyrimidinesReceptor, Platelet-Derived Growth Factor alphaSmall-Conductance Calcium-Activated Potassium Channels

Identifiers

PMID23148317
PMCPMC3577524
OpenAlexW2172186975

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.