Evidence map›Paper›PMID 18161881›Full record

ArticleHepatology (Baltimore, Md.)2008

Microtubule acetylation and stability may explain alcohol-induced alterations in hepatic protein trafficking.

Rohan A Joseph, Blythe D Shepard, George T Kannarkat, Tara M Rutledge, Dean J Tuma, Pamela L Tuma

Open access · bronzeAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.5field-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

27 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  6. Alcohol-induced microtubule acetylation leads to the accumulation of large, immobile lipid droplets.American journal of physiology. Gastrointestinal and liver physiology · 2019
    Article
  7. Review
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  10. Ethanol metabolism by alcohol dehydrogenase or cytochrome PAmerican journal of physiology. Gastrointestinal and liver physiology · 2017
    Article
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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 3 institutions in 1 country.

Rohan A JosephDepartment of Biology, The Catholic University of America, Washington, DC 20064, USA.
Blythe D Shepard
George T Kannarkat
Tara M Rutledge
Dean J Tuma
Pamela L Tuma
Catholic University of America · USUniversity of America · USUniversity of Nebraska Medical Center · US

Funding

Alcohol alters hepatic microtubule and membrane dynamicsR21AA015683 · NIAAA · CATHOLIC UNIVERSITY OF AMERICA · PI TUMA, PAMELA L · 2005 to 2006
$349k
NIAAA NIH HHS R21 AA015683
6 · The paper itself

Abstract

unlabelledWe have been using polarized hepatic WIF-B cells to examine ethanol-induced liver injury. Previously, we determined microtubules were more highly acetylated and more stable in ethanol-treated WIF-B cells. We proposed that the ethanol-induced alterations in microtubule dynamics may explain the ethanol-induced defects in membrane trafficking that have been previously documented. To test this, we compared the trafficking of selected proteins in control cells and cells treated with ethanol or with the histone deacetylase 6 inhibitor trichostatin A (TSA). We determined that exposure to 50 nM TSA for 30 minutes induced microtubule acetylation ( approximately 3-fold increase) and stability to the same extent as did ethanol. As shown previously in situ, the endocytic trafficking of the asialoglycoprotein receptor (ASGP-R) was impaired in ethanol-treated WIF-B cells. This impairment required ethanol metabolism and was likely mediated by acetaldehyde. TSA also impaired ASGP-R endocytic trafficking, but to a lesser extent. Similarly, both ethanol and TSA impaired transcytosis of the single-spanning apical resident aminopeptidase N (APN). For both ASGP-R and APN and for both treatments, the block in trafficking was internalization from the basolateral membrane. Interestingly, no changes in transcytosis of the glycophosphatidylinositol-anchored protein, 5'-nucleotidase, were observed, suggesting that increased microtubule acetylation and stability differentially regulate internalization. We further determined that albumin secretion was impaired in both ethanol-treated and TSA-treated cells, indicating that increased microtubule acetylation and stability also disrupted this transport step.

conclusionThese results indicate that altered microtubule dynamics explain in part alcohol-induced defects in membrane trafficking.

Indexed as

AcetylationAnimalsCarcinoma, HepatocellularEthanolHistone Deacetylase InhibitorsHydroxamic AcidsKineticsLiverLiver NeoplasmsMicrotubulesProteinsRatsSerum AlbuminEthanolHistone Deacetylase InhibitorsHydroxamic AcidsProteinsSerum Albumintrichostatin A

Identifiers

PMID18161881
PMCPMC2957806
OpenAlexW1970977249

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.