Evidence map›Paper›PMID 7622559›Full record

ArticleThe Journal of cell biology1995

Insulation of a G protein-coupled receptor on the plasmalemmal surface of the pancreatic acinar cell.

B F Roettger, R U Rentsch, E M Hadac, E H Hellen, T P Burghardt, L J Miller

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Differential binding profile and internalization process of neurotensin via neuronal and glial receptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1997
    Article
  12. Review
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

6 authors at 1 institution in 1 country.

B F RoettgerCenter for Basic Research in Digestive Diseases, Mayo Clinic and Foundation, Rochester, Minnesota 55905, USA.
R U Rentsch
E M Hadac
E H Hellen
T P Burghardt
L J Miller
Mayo Clinic · US

Funding

Type A CCK Receptor Structure, Function and RegulationR37DK032878 · NIDDK · MAYO CLINIC COLL OF MED, MAYO CLINIC AZ · PI MILLER, LAURENCE J · 2001 to 2010
$4.5M
Type A CCK Receptor Structure, Function & RegulationR01DK032878 · NIDDK · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI MILLER, LAURENCE J · 1986 to 2014
$2.5M
MOLECULAR ANGLE TRANSITIONS IN MUSCLER01AR039288 · NIAMS · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI BURGHARDT, THOMAS P · 1990 to 2001
$448k
INTERNALIZATION PATHWAYS OF THE PANCREATIC CCK RECEPTORF32DK009078 · NIDDK · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI ROETTGER, BELINDA F · 1994 to 1995
–
NIAMS NIH HHS AR39288NIDDK NIH HHS DK09078NIDDK NIH HHS DK32878
6 · The paper itself

Abstract

Receptor desensitization is a key process for the protection of the cell from continuous or repeated exposure to high concentrations of an agonist. Well-established mechanisms for desensitization of guanine nucleotide-binding protein (G protein)-coupled receptors include phosphorylation, sequestration/internalization, and down-regulation. In this work, we have examined some mechanisms for desensitization of the cholecystokinin (CCK) receptor which is native to the pancreatic acinar cell, and have found the predominant mechanism to be distinct from these recognized processes. Upon fluorescent agonist occupancy of the native receptor, it becomes "insulated" from the effects of acid washing and becomes immobilized on the surface of the plasma membrane in a time- and temperature-dependent manner. This localization was assessed by ultrastructural studies using a colloidal gold conjugate of CCK, and lateral mobility of the receptor was assessed using fluorescence recovery after photobleaching. Of note, recent application of the same morphologic techniques to a CCK receptor-bearing Chinese hamster ovary cell line demonstrated prominent internalization via the clathrin-dependent endocytic pathway, as well as entry into caveolae (Roettger, B.F., R.U. Rentsch, D. Pinon, E. Holicky, E. Hadac, J.M. Larkin, and L.J. Miller, 1995, J. Cell Biol. 128: 1029-1041). These organelles are not observed to represent prominent compartments for the same receptor to traverse in the acinar cell, although fluorescent insulin is clearly internalized in these cells via receptor-mediated endocytosis. In this work, the rate of lateral mobility of the CCK receptor is observed to be similar in both cell types (1-3 x 10(-10) cm2/s), while the fate of the agonist-occupied receptor is quite distinct in each cell. This supports the unique nature of desensitization processes which occur in a cell-specific manner. A plasmalemmal site of insulation of this important receptor on the pancreatic acinar cell could be particularly effective to protect the cell from processes which might initiate pancreatitis, while providing for the rapid resensitization of this receptor to ensure appropriate pancreatic secretion to aid in nutrient assimilation for the organism.

Indexed as

AcidsAnimalsCell MembraneCHO CellsCholecystokininCricetinaeFluorescent DyesGTP-Binding ProteinsHistocytochemistryHot TemperatureMaleMembrane FluidityMicroscopy, ConfocalMicroscopy, ElectronMicroscopy, FluorescenceMotionAcidsCholecystokininFluorescent DyesGTP-Binding ProteinsReceptors, Cholecystokinin

Identifiers

PMID7622559
PMCPMC2120534
OpenAlexW1980730059

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.