Evidence map›Paper›PMID 19184252›Full record

ArticleIn vitro cellular & developmental biology. Animal

Macrophage cell lines use CD81 in cell growth regulation.

Whitney J Mordica, Keith M Woods, Rollie J Clem, A Lorena Passarelli, Stephen K Chapes

Abstract read
In one paragraph

Article in In vitro cellular & developmental biology. Animal. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 43% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. CD81 inhibits the proliferation of astrocytes by inducing G(0)/G (1) arrest in vitro.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2010
    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 1 institution in 1 country.

Whitney J MordicaDivision of Biology, Kansas State University, 116 Ackert Hall, Manhattan, KS 66506-4901, USA.
Keith M Woods
Rollie J Clem
A Lorena Passarelli
Stephen K Chapes
Kansas State University · US

Funding

UNDERSTANDING THE ROLE OF SMALL RNAS IN ARABIDOPSIS POLLEN DEVELOPMENTP20RR016475 · NCRR · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ACKLEY, BRIAN DOUGLAS · 2001 to 2011
$38.1M
TRANSEPITHELIAL ION TRANSPORT &ITS REGULATIONP20RR017686 · NCRR · KANSAS STATE UNIVERSITY · PI MELGAREJO GARCIA, LUIS TONATIUH · 2002 to 2011
$21.8M
Cellular Immunity Against Ehrlichia chaffeensisR01AI055052 · NIAID · KANSAS STATE UNIVERSITY · PI GANTA, ROMAN R. · 2003 to 2007
$1.5M
Analysis of CD81-PGRL complex on T cellsR01AI052206 · NIAID · KANSAS STATE UNIVERSITY · PI CHAPES, STEPHEN KEITH · 2003 to 2007
$1.3M
NCRR NIH HHS P20 RR016475NCRR NIH HHS P20 RR017686NCRR NIH HHS RR16475NCRR NIH HHS RR17686NIAID NIH HHS AI052206NIAID NIH HHS AI55052NIAID NIH HHS R01 AI052206NIAID NIH HHS R01 AI055052
6 · The paper itself

Abstract

CD81 is an integral membrane protein belonging to the tetraspanin superfamily. It has two extracellular domains that interact with cell surface proteins and two intracellular tails that contribute to cellular processes. Although there are considerable data about how CD81 affects T- and B-cell function, not much is known about how it impacts macrophages. To address this, we established four cell lines from mouse bone marrow in the presence of macrophage colony-stimulating factor and transfection with SV40 large T antigen. Two were CD81(-/-) (ASD1 and ASD2) and two were CD81(+/-) (2ASD1.10 and 2BSD1.10). Cells were Mac-2-, PU.1-, and c-fms-positive and all the cell lines were phagocytic indicating that they were macrophage-like. In mixtures of the two cell types in tissue culture, CD81(-/-) cells out competed CD81(+/-) cells with CD81-bearing cells being undetectable after 50 cell culture passages. Although cell divisions during log-phase growth were not significantly different between CD81(+/-) macrophage cells and CD81(-/-) macrophage cells, we found that CD81(-/-) macrophage cells reached a higher density at confluency than CD81(+/-) macrophage cells. CD81 transcript levels increased as cultures became confluent, but transcript levels of other tetraspanin-related molecules remained relatively constant. Transfection of CD81 into ASD1 (CD81(-/-)) cells reduced the density of confluent cultures of transformants compared to cells transfected with vector alone. These data suggest that CD81 potentially plays a role in macrophage cell line growth regulation.

Indexed as

AnimalsAntigens, CDCell DivisionCell LineCell LineageCell MembraneCell ProliferationCell SeparationFemaleGenotypeMacrophagesMaleMicePhagocytosisPhenotypeTetraspanin 28Antigens, CDCd81 protein, mouseTetraspanin 28

Identifiers

PMID19184252
PMCPMC3595608
OpenAlexW1987395525

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.