Evidence map›Paper›PMID 42193890›Full record

ArticleCells2026

A Novel Selective Strategy for Bioactive Limbal Stem Cells Primary Culture Using Deep Cryopreservation and IL-1β Precondition.

Yinglin Liu, Liling Xu, Yanmei Li, Cheng Lu, Zepei Fan, Jun Ling, Yingwei Wang, Zheng Wu

Abstract read
In one paragraph

Article in Cells, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Yinglin LiuKey Laboratory for Regenerative Medicine, Ministry of Education, Department of Developmental and Regenerative Biology, Jinan University, Guangzhou 510630, China.
Liling XuKey Laboratory for Regenerative Medicine, Ministry of Education, Department of Developmental and Regenerative Biology, Jinan University, Guangzhou 510630, China.ORCID 0000-0002-7572-4455
Yanmei LiKey Laboratory for Regenerative Medicine, Ministry of Education, Department of Developmental and Regenerative Biology, Jinan University, Guangzhou 510630, China.ORCID 0009-0001-7964-6095
Cheng LuKey Laboratory for Regenerative Medicine, Ministry of Education, Department of Developmental and Regenerative Biology, Jinan University, Guangzhou 510630, China.
Zepei FanKey Laboratory for Regenerative Medicine, Ministry of Education, Department of Developmental and Regenerative Biology, Jinan University, Guangzhou 510630, China.
Jun LingKey Laboratory for Regenerative Medicine, Ministry of Education, Department of Developmental and Regenerative Biology, Jinan University, Guangzhou 510630, China.
Yingwei WangKey Laboratory for Regenerative Medicine, Ministry of Education, Department of Developmental and Regenerative Biology, Jinan University, Guangzhou 510630, China.
Zheng WuKey Laboratory for Regenerative Medicine, Ministry of Education, Department of Developmental and Regenerative Biology, Jinan University, Guangzhou 510630, China.

Funding

China Postdoctoral Science Foundation 2025M782898Guangdong Basic and Applied Basic Research Foundation 2024A1515011167National Natural Science Foundation of China 32371418National Natural Science Foundation of China 82301172
6 · The paper itself

Abstract

Limbal stem cell (LSC) transplantation is an important treatment for limbal stem cell deficiency (LSCD), but low efficacy in maintaining LSC stemness during in vitro expansion greatly affects its wider application. The primary contributing factors include a low proportion of stem cells and the lack of a stable, supportive microenvironment over prolonged culture. Rabbit corneal tissues preserved under deep cryogenic conditions for more than six months retain viable limbal stem cells (LSCs), and primary LSCs isolated from these tissues exhibit robust stem cell characteristics. It is noteworthy that the NLRP3/Caspase-1/IL-1β signaling axis was activated in corneal epithelial cells, and outer limbal layers preserved for one or two years. Based on these findings, a combined strategy integrating deep cryopreservation with IL-1β induction was established for the processing of limbal tissues. The combined cryogenic and IL-1β preconditioning yielded primary LSCs with maintained p63

Indexed as

CryopreservationInterleukin-1betaLimbal Stem CellsLimbus CorneaePrimary Cell CultureStem CellsAnimalsCell DifferentiationCell ProliferationLimbal Stem Cell DeficiencyRabbitsInterleukin-1betacryogenic inductioncryopreservationinflammatory factor inductionlimbal stem cellsprimary cell culture

Identifiers

PMID42193890
PMCPMC13205095

What OpenQuestion holds

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LicenceCC BY
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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.