Evidence map›Paper›PMID 7506266›Full record

ArticleThe Journal of cell biology1993

WIF-B cells: an in vitro model for studies of hepatocyte polarity.

G Ihrke, E B Neufeld, T Meads, M R Shanks, D Cassio, M Laurent, T A Schroer, R E Pagano, A L Hubbard

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

82 citing papers in PubMed, 209 citations in OpenAlex.

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  10. Manganese transport and toxicity in polarized WIF-B hepatocytes.American journal of physiology. Gastrointestinal and liver physiology · 2018
    Article
  11. Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2018
    Article
  12. Article
  13. Ethanol metabolism by alcohol dehydrogenase or cytochrome PAmerican journal of physiology. Gastrointestinal and liver physiology · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

22 more citing papers are in PubMed but not listed here.

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

9 authors at 1 institution in 1 country.

G IhrkeDepartment of Cell Biology and Anatomy, Johns Hopkins School of Medicine, Baltimore, Maryland 21205.
E B Neufeld
T Meads
M R Shanks
D Cassio
M Laurent
T A Schroer
R E Pagano
A L Hubbard
Johns Hopkins University · US

Funding

TARGETING OF MEMBRANE PROTEINS IN POLARIZED EPITHELIAP01DK044375 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI HUBBARD, ANN L · 1992 to 2002
$3.0M
NIDDK NIH HHS DK 44375
6 · The paper itself

Abstract

We have evaluated the utility of the hepatoma-derived hybrid cell line, WIF-B, for in vitro studies of polarized hepatocyte functions. The majority (> 70%) of cells in confluent culture formed closed spaces with adjacent cells. These bile canalicular-like spaces (BC) accumulated fluorescein, a property of bile canaliculi in vivo. By indirect immunofluorescence, six plasma membrane (PM) proteins showed polarized distributions similar to rat hepatocytes in situ. Four apical PM proteins were concentrated in the BC membrane of WIF-B cells. Microtubules radiated from the BC (apical) membrane, and actin and foci of gamma-tubulin were concentrated in this region. The tight junction-associated protein ZO-1 was present in belts marking the boundary between apical and basolateral PM domains. We explored the functional properties of this boundary in living cells using fluorescent membrane lipid analogs and soluble tracers. When cells were incubated at 4 degrees C with a fluorescent analog of sphingomyelin, only the basolateral PM was labeled. In contrast, when both PM domains were labeled by de novo synthesis of fluorescent sphingomyelin from ceramide, fluorescent lipid could only be removed from the basolateral domain. These data demonstrate the presence of a barrier to the lateral diffusion of lipids between the PM domains. However, small soluble FITC-dextrans (4,400 mol wt) were able to diffuse into BC, while larger FITC-dextrans were restricted to various degrees depending on their size and incubation temperature. At 4 degrees C, the surface labeling reagent sNHS-LC-biotin (557 mol wt) had access to the entire PM, but streptavidin (60,000 mol wt), which binds to biotinylated molecules, was restricted to only the basolateral domain. Such differential accessibility of well-characterized probes can be used to mark each membrane domain separately. These results show that WIF-B cells are a suitable model to study membrane trafficking and targeting in hepatocytes in vitro.

Indexed as

AnimalsCarcinoma, HepatocellularCell MembraneCells, CulturedCeramidesDextransFluorescein-5-isothiocyanateFluorescent Antibody TechniqueHumansHybrid CellsIntercellular JunctionsLiverLiver NeoplasmsMembrane ProteinsMicrotubulesModels, BiologicalCeramidesDextransFluorescein-5-isothiocyanatefluorescein isothiocyanate dextranMembrane ProteinsPhosphoproteinsSphingolipidsSphingomyelinsTJP1 protein, humanTjp1 protein, ratZonula Occludens-1 Protein

Identifiers

PMID7506266
PMCPMC2290861
OpenAlexW2113189847

What OpenQuestion holds

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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.