Evidence map›Paper›PMID 22936272›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2012

Cell-specific effects of luminal acid, bicarbonate, cAMP, and carbachol on transporter trafficking in the intestine.

Robert L Jakab, Anne M Collaco, Nadia A Ameen

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Characterization of CFTR High Expresser cells in the intestine.American journal of physiology. Gastrointestinal and liver physiology · 2013
    Article
  10. Regulated traffic of anion transporters in mammalian Brunner's glands: a role for water and fluid transport.American journal of physiology. Gastrointestinal and liver physiology · 2013
    Article
  11. 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 1 institution in 1 country.

Robert L JakabDepartment of Pediatrics/Gastroenterology and Hepatology, School of Medicine, New Haven, Connecticut 06520, USA.
Anne M Collaco
Nadia A Ameen
Yale University · US

Funding

Yale Liver CenterP30DK034989 · NIDDK · YALE UNIVERSITY · PI YASUKO IWAKIRI · 1986 to 2026
$31.1M
Renal Physiology and Phenotyping CoreP30DK079310 · NIDDK · YALE UNIVERSITY · PI ARONSON, PETER S. · 2008 to 2022
$16.8M
Glucocorticoid and SGK1 regulation of CFTR in the intestine: role in diarrheaR01DK077065 · NIDDK · YALE UNIVERSITY · PI AMEEN, NADIA A. · 2008 to 2024
$5.8M
NIDDK NIH HHS DK-34989NIDDK NIH HHS P30 DK079310NIDDK NIH HHS R01-DK-077065
6 · The paper itself

Abstract

Changes in intestinal luminal pH affect mucosal ion transport. The aim of this study was to compare how luminal pH and specific second messengers modulate the membrane traffic of four major ion transporters (CFTR, NHE3, NKCC1, and NBCe1) in rat small intestine. Ligated duodenal, jejunal, and ileal segments were infused with acidic or alkaline saline, 8-Br-cAMP, or the calcium agonist carbachol in vivo for 20 min. Compared with untreated intestine, lumen pH was reduced after cAMP or carbachol and increased following HCO(3)(-)-saline. Following HCl-saline, lumen pH was restored to control pH levels. All four secretory stimuli resulted in brush-border membrane (BBM) recruitment of CFTR in crypts and villi. In villus enterocytes, CFTR recruitment was coincident with internalization of BBM NHE3 and basolateral membrane recruitment of the bicarbonate transporter NBCe1. Both cAMP and carbachol recruited NKCC1 to the basolateral membrane of enterocytes, while luminal acid or HCO(3)(-) retained NKCC1 in intracellular vesicles. Luminal acid resulted in robust recruitment of CFTR and NBCe1 to their respective enterocyte membrane domains in the upper third of the villi; luminal HCO(3)(-) induced similar membrane changes lower in the villi. These findings indicate that each stimulus promotes a specific transporter trafficking response along the crypt-villus axis. This is the first demonstration that physiologically relevant secretory stimuli exert their actions in villus enterocytes by membrane recruitment of CFTR and NBCe1 in tandem with NHE3 internalization.

Indexed as

8-Bromo Cyclic Adenosine MonophosphateAcidsAnimalsBicarbonatesCarbacholCystic Fibrosis Transmembrane Conductance RegulatorHumansIntestinal MucosaIntestinesMaleProtein TransportRatsRats, Sprague-DawleySodium-Bicarbonate SymportersSodium-Hydrogen Exchanger 3Sodium-Hydrogen Exchangers8-Bromo Cyclic Adenosine MonophosphateAcidsBicarbonatesCarbacholCystic Fibrosis Transmembrane Conductance RegulatorSLC12A2 protein, humanSlc12a2 protein, ratSlc4a4 protein, ratSLC9A3 protein, humanSlc9a3 protein, ratSodium-Bicarbonate SymportersSodium-Hydrogen Exchanger 3Sodium-Hydrogen ExchangersSodium-Potassium-Chloride SymportersSolute Carrier Family 12, Member 2

Identifiers

PMID22936272
PMCPMC3469693
OpenAlexW2057262607

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.