Evidence map›Paper›PMID 27005832›Full record

ArticleJournal of proteome research2016

Utilization of HPASubC for the Identification of Sinusoid-Specific Proteins in the Liver.

Divine-Favour Anene, Avi Z Rosenberg, David E Kleiner, Toby C Cornish, Marc K Halushka

Open access · greenAbstract read
In one paragraph

Article in Journal of proteome research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Cardiomyocytes have mosaic patterns of protein expression.Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology
    Article
  4. An expanded proteome of cardiac t-tubules.Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology
    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

5 authors at 4 institutions in 1 country.

Divine-Favour AneneDepartment of Pathology, Johns Hopkins University School of Medicine , 720 Rutland Avenue, Baltimore, Maryland 21205, United States.
Avi Z RosenbergDepartment of Pathology, Children's National Medical Center , 111 Michigan Avenue Northwest, Washington, D.C. 20010, United States.
David E KleinerLaboratory of Pathology, National Cancer Institute , Building 10, Room 2S235, MSC 1500, 10 Center Drive, Bethesda, Maryland 20892, United States.
Toby C CornishDepartment of Pathology, Johns Hopkins University School of Medicine , 720 Rutland Avenue, Baltimore, Maryland 21205, United States.
Marc K HalushkaDepartment of Pathology, Johns Hopkins University School of Medicine , 720 Rutland Avenue, Baltimore, Maryland 21205, United States.
Johns Hopkins University · USChildren's National · USJohns Hopkins Medicine · USNational Cancer Institute · US

Funding

Postmortem PathologyZ01BC010685 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KLEINER, DAVID E · 2005 to 2008
$913k
Intramural NIH HHS Z01 BC010685
6 · The paper itself

Abstract

Mass spectrometry-based proteomes of human organs and tissues are powerful tools but fail to capture protein localization and expression at the cellular level. For example, the proteome signal in liver represents the combined protein expression across diverse cellular constituents that include hepatocytes, Kupffer cells, endothelial cells, and others. We utilized HPASubC and the Human Protein Atlas (HPA) to identify the sinusoidal component of protein liver expression to further subset and organize this homogeneous signal. We evaluated 51 109 liver images covering 13 197 proteins from the HPA and discovered 1054 proteins that were exclusive to sinusoidal cells. Sinusoidal staining patterns were identified in a Kupffer cell (n = 247), endothelial cell (n = 358), or lymphocyte (n = 86) specific pattern. Two-hundred and thirty-nine of these proteins were not present in the NextProt or Human Proteome Map liver data sets, potentially expanding our knowledge of the liver proteome. We additionally demonstrate unique endothelial cell expression patterns that distinguish between portal vein, hepatic artery, capillary sinusoids, and central vein regions. These findings significantly improve our understanding of the liver proteome with insight into the endothelial complexity across the hepatic vascular network.

Indexed as

CapillariesData MiningEndothelium, VascularHumansKupffer CellsLiverLymphocytesProteomeProteomeendothelial cellHPASubChuman protein atlasKupffer cellliverlymphocyteproteometissue microarray

Identifiers

PMID27005832
PMCPMC8201909
OpenAlexW2309610704

What OpenQuestion holds

Textmetadata
LicenceTDM
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.