Evidence map›Paper›PMID 21178145›Full record

ArticleInvestigative ophthalmology & visual science2011

Isolation and propagation of mesenchymal stem cells from the lacrimal gland.

Samantha You, Claire L Kublin, Orna Avidan, David Miyasaki, Driss Zoukhri

Open access · bronzeAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

28 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
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  4. Review
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  8. Article
  9. Establishing and characterizing lacrispheres from human lacrimal gland for potential clinical application.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2018
    Article
  10. Lacrimal gland development: From signaling interactions to regenerative medicine.Developmental dynamics : an official publication of the American Association of Anatomists · 2017
    Review
  11. Strategies for Regenerating the Lacrimal Gland.Current ophthalmology reports · 2017
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Lacrimal Gland Repair Using Progenitor Cells.Stem cells translational medicine · 2017
    Article
  17. Article
  18. Article
  19. Bioengineered Lacrimal Gland Organ Regeneration in Vivo.Journal of functional biomaterials · 2015
    Article
  20. Human lacrimal gland regeneration: Perspectives and review of literature.Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society · 2014
    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.

Samantha YouDepartment of General Dentistry, Tufts University School of Dental Medicine, Boston, Massachusetts 02111, USA.
Claire L Kublin
Orna Avidan
David Miyasaki
Driss Zoukhri
Tufts University · US

Funding

STIMULUS/SECRETION COUPLING IN DISEASED LACRIMAL GLANDR01EY012383 · NEI · TUFTS UNIVERSITY BOSTON · PI ZOUKHRI, DRISS · 1999 to 2015
$5.2M
NEI NIH HHS R01 EY012383NEI NIH HHS R01-EY12383
6 · The paper itself

Abstract

purposePreviously, it was reported that the murine lacrimal gland is capable of repair after experimentally induced injury and that the number of stem/progenitor cells was increased during the repair phase (2-3 days after injury). The aim of the present study was to determine whether these cells can be isolated from the lacrimal gland and propagated in vitro.

methodsLacrimal gland injury was induced by injection of interleukin (IL)-1, and injection of saline vehicle served as control. Two and half days after injection, the lacrimal glands were removed and used to prepare explants or acinar cells for tissue culture. Cells derived from the explants and the acinar cells were grown in DMEM supplemented with 10% fetal bovine serum. Cells were stained for the stem cells markers, nestin, vimentin, ABCG2, and Sca-1. Cell proliferation was measured using an antibody against Ki67 or a cell-counting kit. The adipogenic capability of these cells was also tested in vitro.

resultsResults show that nestin-positive cells can be isolated from IL-1-injected, but not saline-injected, lacrimal glands. A population of nestin-positive cells was also positive for vimentin, an intermediate filament protein expressed by mesenchymal cells. In addition, cultured cells expressed two other markers of stem cells, ABCG2 and Sca-1. These cells proliferated in vitro and can be induced to form adipocytes, attesting to their mesenchymal stem cell property.

conclusionsMurine lacrimal glands contain mesenchymal stem cells that seem to play a pivotal role in tissue repair.

Indexed as

AdipogenesisAnimalsAntigens, LyATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily G, Member 2BiomarkersCell CountCell Culture TechniquesCell ProliferationCell SeparationFemaleFluorescent Antibody Technique, IndirectIntermediate Filament ProteinsKi-67 AntigenLacrimal ApparatusMembrane ProteinsAbcg2 protein, mouseAntigens, LyATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily G, Member 2BiomarkersIntermediate Filament ProteinsKi-67 AntigenLy6a protein, mouseMembrane ProteinsNerve Tissue ProteinsNes protein, mouseNestinVimentin

Identifiers

PMID21178145
PMCPMC3080180
OpenAlexW1975884685

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.