Evidence map›Paper›PMID 40064928›Full record

ArticleScientific reports2025

Autologous serum supplementation promotes the phenotype maintenance of human chondrocytes with increased cellular autophagy.

Wei Yin, Zhigang Qian, Chun Liu, Baishan Song, Qicai Sun

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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.

Wei YinZhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Zhigang QianDepartment of Orthopaedic Surgery, Zhejiang Hospital, Hangzhou, Zhejiang, China.
Chun LiuDepartment of Orthopaedic Surgery, Zhejiang Hospital, Hangzhou, Zhejiang, China.
Baishan SongDepartment of Orthopaedic Surgery, Zhejiang Hospital, Hangzhou, Zhejiang, China.
Qicai SunDepartment of Orthopaedic Surgery, Zhejiang Hospital, Hangzhou, Zhejiang, China. sunqicai20718170@126.com.

Funding

Zhejiang Medical and Health Science and Technology Project 2022B12
6 · The paper itself

Abstract

Articular cartilage lacks the capacity for self-repair after injury, rendering autologous chondrocyte transplantation a crucial treatment option for severe cartilage damage. However, the in vitro expansion of chondrocytes in elderly patients poses challenges, particularly due to inadequate cell numbers and rapid phenotypic loss, often exacerbated by the use of animal-derived serum. In this study, we propose the utilization of human autologous serum (HAS) as a supplement in the in vitro cell culture to preserve the phenotype of chondrocytes isolated from the same patient. Chondrocytes cultured in medium supplemented with 5% HAS demonstrated improved cell proliferation and adherence, whereas a 10% concentration promoted a more differentiated phenotype. While 10% fetal bovine serum stimulates chondrocyte proliferation in the short term, 10% HAS is more advantageous for the long-term viability of cells. Notably, chondrocytes treated with the optimal 10% HAS supplementation exhibited a higher level of autophagy compared to those treated with 5% HAS alone. Our findings suggest that 10% human autologous serum holds promise for the efficient expansion of patient-derived autologous chondrocytes and facilitates the maintenance of chondrocyte phenotype, in part through enhanced cellular autophagy.

Indexed as

AutophagyChondrocytesCulture MediaSerumCartilage, ArticularCell Culture TechniquesCell DifferentiationCell ProliferationCells, CulturedCell SurvivalHumansPhenotypeCulture MediaHuman autologous serumHuman chondrocytesIn vitro culture

Identifiers

PMID40064928
PMCPMC11894040

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.