Evidence map›Paper›PMID 19593795›Full record

ArticleStem cells (Dayton, Ohio)2009

Importin 13 serves as a potential marker for corneal epithelial progenitor cells.

Hua Wang, Tao Tao, Jing Tang, Yi-Hui Mao, Wei Li, Juan Peng, Gang Tan, Yue-Ping Zhou, Jing-Xiang Zhong, Scheffer C G Tseng and 3 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Karyopherins in cancer.Current opinion in cell biology · 2018
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Expression and subcellular distribution of imp13 are regulated in brain development.In vitro cellular & developmental biology. Animal · 2013
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Increased expression of importin13 in endometriosis and endometrial carcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2012
    Article
  15. Article
  16. Review
  17. The expression levels of stem cell markers importin13, c-kit, CD146, and telomerase are decreased in endometrial polyps.Medical science monitor : international medical journal of experimental and clinical research · 2011
    Article
  18. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 3 countries.

Hua WangEye Institute and Affiliated Xiamen Eye Center, Xiamen University, Xiamen, Fujian, China.
Tao Tao
Jing Tang
Yi-Hui Mao
Wei Li
Juan Peng
Gang Tan
Yue-Ping Zhou
Jing-Xiang Zhong
Scheffer C G Tseng
Tetsuya Kawakita
Yong-Xiang Zhao
Zu-Guo Liu
Xiamen University · CNZhongshan Hospital of Xiamen University · CNKeio University · JPOcular Surface Center · US

Funding

VITAMIN A AND CONJUNCTIVAL TRANSDIFFERENTIATIONR01EY006819 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI TSENG, SCHEFFER CG · 1986 to 2020
$6.7M
NEI NIH HHS R01 EY006819
6 · The paper itself

Abstract

Importin13 (IPO13), the newest member of importin-beta family discovered recently, is a unique nucleus-cytoplasm bidirectional transport receptor protein. In this study, IPO13 expression in human corneal tissue, limbal epithelial primary explant and clonal culture was evaluated by immunostaining and reverse-transcription polymerase chain reasgon. IPO13 function was evaluated in the corneal epithelial culture treated with IPO13 inhibitor, or fetal bovine serum (FBS)-containing Dulbecco's modified Eagle's medium (DMEM) medium by colony-forming efficiency, clone growth capacity, MTT, immunostaining, and Western blotting assay. IPO13 protein was expressed mainly in nuclei of limbal epithelial basal cells, but not in the other cell layers of limbus and full thickness of corneal epithelia. IPO13 was expressed in the majority of epithelial cells in early-stage clones and in the margin of late-stage clones. IPO13 was positively expressed in mouse TKE2 progenitor cells cultured in keratinocyte serum-free defined medium, while it became negative in FBS-containing DMEM, which promoted TKE2 cell differentiation. In the presence of IPO13 inhibitor, IPO13 expression and the proliferative capacity decreased in human limbal epithelial clones and mouse TKE2 cells, which were accompanied with the cell differentiation. In conclusion, our findings demonstrate for the first time that IPO13 is uniquely expressed by human limbal basal epithelial cells, and plays an important role in maintaining the phenotype, high proliferative potential, and less differentiation of corneal epithelial progenitor cells, suggesting that IPO13 could serve as a novel potential marker for corneal epithelial progenitor cells.

Indexed as

Cell ProliferationAdolescentAdultAnimalsBiomarkersCell DifferentiationCells, CulturedEpithelium, CornealGrowth InhibitorsHumansImmunohistochemistryKaryopherinsMiceMiddle AgedNIH 3T3 CellsPhenotypeBiomarkersGrowth InhibitorsIPO13 protein, humanKaryopherinsRNA, Messenger

Identifiers

PMID19593795
PMCPMC2846104
OpenAlexW2083310304

What OpenQuestion holds

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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.