Evidence map›Paper›PMID 24578340›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2014

Myosin IIB and F-actin control apical vacuolar morphology and histamine-induced trafficking of H-K-ATPase-containing tubulovesicles in gastric parietal cells.

Paramasivam Natarajan, James M Crothers, Jared E Rosen, Stephanie L Nakada, Milap Rakholia, Curtis T Okamoto, John G Forte, Terry E Machen

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

8 authors at 2 institutions in 1 country.

Paramasivam NatarajanDepartment of Molecular and Cell Biology, University of California, Berkeley, California; and.
James M Crothers
Jared E Rosen
Stephanie L Nakada
Milap Rakholia
Curtis T Okamoto
John G Forte
Terry E Machen
University of California, Berkeley · USUniversity of Southern California · US

Funding

MECHANISM OF H+ AND CL- TRANSPORT BY GASTRIC MUCOSAR01AM010141 · AM · UNIVERSITY OF CALIFORNIA BERKELEY · PI FORTE, JOHN G · 1985 to 1985
–
NIADDK NIH HHS AM-10141
6 · The paper itself

Abstract

Selective inhibitors of myosin or actin function and confocal microscopy were used to test the role of an actomyosin complex in controlling morphology, trafficking, and fusion of tubulovesicles (TV) containing H-K-ATPase with the apical secretory canaliculus (ASC) of primary-cultured rabbit gastric parietal cells. In resting cells, myosin IIB and IIC, ezrin, and F-actin were associated with ASC, whereas H-K-ATPase localized to intracellular TV. Histamine caused fusion of TV with ASC and subsequent expansion resulting from HCl and water secretion; F-actin and ezrin remained associated with ASC whereas myosin IIB and IIC appeared to dissociate from ASC and relocalize to the cytoplasm. ML-7 (inhibits myosin light chain kinase) caused ASC of resting cells to collapse and most myosin IIB, F-actin, and ezrin to dissociate from ASC. TV were unaffected by ML-7. Jasplakinolide (stabilizes F-actin) caused ASC to develop large blebs to which actin, myosin II, and ezrin, as well as tubulin, were prominently localized. When added prior to stimulation, ML-7 and jasplakinolide prevented normal histamine-stimulated transformations of ASC/TV and the cytoskeleton, but they did not affect cells that had been previously stimulated with histamine. These results indicate that dynamic pools of actomyosin are required for maintenance of ASC structure in resting cells and for trafficking of TV to ASC during histamine stimulation. However, the dynamic pools of actomyosin are not required once the histamine-stimulated transformation of TV/ASC and cytoskeleton has occurred. These results also show that vesicle trafficking in parietal cells shares mechanisms with similar processes in renal collecting duct cells, neuronal synapses, and skeletal muscle.

Indexed as

Parietal Cells, GastricTransport VesiclesActinsAnimalsAzepinesBiological TransportCell Physiological PhenomenaCells, CulturedEnzyme InhibitorsH(+)-K(+)-Exchanging ATPaseNaphthalenesNonmuscle Myosin Type IIBRabbitsActinsAzepinesEnzyme InhibitorsH(+)-K(+)-Exchanging ATPaseML 7NaphthalenesNonmuscle Myosin Type IIBF-actinmembrane dynamicsnonmuscle myosin IIvesicle trafficking

Identifiers

PMID24578340
PMCPMC3989701
OpenAlexW2025768306

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.