Evidence map›Paper›PMID 22665974›Full record

ArticleMolecular vision2012

Characterization of cultivated murine lacrimal gland epithelial cells.

Shinya Kobayashi, Tetsuya Kawakita, Motoko Kawashima, Naoko Okada, Kenji Mishima, Ichiro Saito, Masataka Ito, Shigeto Shimmura, Kazuo Tsubota

Open access · greenAbstract read
In one paragraph

Article in Molecular vision, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

10 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Lacrimal gland development: From signaling interactions to regenerative medicine.Developmental dynamics : an official publication of the American Association of Anatomists · 2017
    Review
  5. Strategies for Regenerating the Lacrimal Gland.Current ophthalmology reports · 2017
    Article
  6. Article
  7. Article
  8. Applications of stem cell biology to oculoplastic surgery.Current opinion in ophthalmology · 2016
    Review
  9. Bioengineered Lacrimal Gland Organ Regeneration in Vivo.Journal of functional biomaterials · 2015
    Article
  10. Review
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 2 institutions in 1 country.

Shinya KobayashiDepartment of Ophthalmology, Keio University School of Medicine, Tokyo, Japan.
Tetsuya Kawakita
Motoko Kawashima
Naoko Okada
Kenji Mishima
Ichiro Saito
Masataka Ito
Shigeto Shimmura
Kazuo Tsubota
Keio University · JPNational Defense Medical College · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo date, mouse lacrimal gland epithelial cells have been cultured successfully but only in cases involving newborn mouse lacrimal glands. In this work, we attempted to cultivate and characterize adult mouse lacrimal gland epithelial cells.

methodsLacrimal glands were removed from newborn mice (C57B/6) and isolated lacrimal gland epithelial cells were seeded onto tissue culture treated or low adherent culture dishes in Cnt-07 culture medium with or without cholera toxin. Cultivated cells were characterized by immunostaining with pan-cytokeratin, α-smooth muscle actin, and lactoferrin antibodies. Lacrimal gland cells from 7-week-old green fluorescent protein (GFP) and non-GFP (C57B/6) mice were mixed and seeded onto uncoated dishes to assess sphere-forming efficiency. Cells were also seeded onto 3T3 cell feeder layers to assess colony forming efficiency.

resultsLacrimal gland epithelial cells were selectively cultured with cholera toxin, and cell type was verified by pan-cytokeratin and α-smooth muscle actin immunostaining. Sphere formation from single cells of adult mice was observed using specific medium and low adherent culture dishes. These cells could also undergo colony formation on 3T3 feeder cells.

conclusionsAdult mouse lacrimal gland epithelial cells were successfully cultivated in cholera toxin-containing medium, and were observed to form spheres from single cells.

Indexed as

ActinsAnimalsAnimals, NewbornBALB 3T3 CellsCell Culture TechniquesCell DivisionCholera ToxinEpithelial CellsFeeder CellsKeratinsLacrimal ApparatusLactoferrinMaleMiceMice, Inbred C57BLActinsalpha-smooth muscle actin, mouseCholera ToxinKeratinsLactoferrin

Identifiers

PMID22665974
PMCPMC3365134
OpenAlexW1506078702

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.