Evidence map›Paper›PMID 25884704›Full record

ArticleStem cell research & therapy2015

Comparative analysis of human mesenchymal stem cells from bone marrow and adipose tissue under xeno-free conditions for cell therapy.

Chun-yu Li, Xiao-yun Wu, Jia-bei Tong, Xin-xin Yang, Jing-li Zhao, Quan-fu Zheng, Guo-bin Zhao, Zhi-jie Ma

Registry-linked trialAbstract readComparative Study
In one paragraph

Article in Stem cell research & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05777213 (Effectiveness of Giving Injection of Human Umbilical Cord Secretome in the Case of Trophic Ulcers), which is not on this map. Cited by 210 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
210citing papers in PubMed, 8 pooled it
–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.

NCT05777213 phase1completednot on this mapstarted 2019, after this paper: background citation

Effectiveness of Giving Injection of Human Umbilical Cord Secretome in the Case of Trophic Ulcers (Pre-post Intervention)

TypeinterventionalSponsorYohanes Firmansyah, dr, MH, MMRan2019 to 2023Enrolled27ConditionsTrophic Ulcer, Leprosy, Morbus HansenArmsSecretome
3 · Its place in the literature

Who cites it

210 citing papers in PubMed, 8 syntheses or guidelines pooled it.

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150 more citing papers are in PubMed but not listed here.

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.

Chun-yu LiChina Military Institute of Chinese Medicine, 302 Military Hospital, Beijing, 100039, China. chunyu327@163.com.
Xiao-yun WuBeijing Institute of Life Science Translational Medicine Research Center, Beijing, 100085, China. chinastemcells@163.com.
Jia-bei TongShandong Medicinal Biotechnology Centre, Shandong Academy of Medical Sciences, Jinan, 250000, China. virosome@163.com.
Xin-xin YangSchool of Pharmacy, Changchun University of Traditional Chinese Medicine, Changsha, 410208, China. xinxin_yang1980@126.com.
Jing-li ZhaoJilin Vocational College of Industry and Technology, Jilin, 132013, China. jinglizhao2005@126.com.
Quan-fu ZhengChina Military Institute of Chinese Medicine, 302 Military Hospital, Beijing, 100039, China. ringring12@126.com.
Guo-bin ZhaoThe First Affiliated Hospital, Hebei North University, Zhangjiakou, 075000, China. 26609642@qq.com.
Zhi-jie MaDepartment of Pharmacy, Beijing Friendship Hospital, Capital Medical University, Beijing, 100050, China. 13811647091@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMesenchymal stem cells (MSCs) are promising candidates for cell-based therapies. Human platelet lysate represents an efficient alternative to fetal bovine serum for clinical-scale expansion of MSCs. Different media used in culture processes should maintain the biological characteristics of MSCs during multiple passages. However, bone marrow-derived MSCs and adipose tissue-derived MSCs have not yet been directly compared with each other under human platelet lysate conditions. This study aims to conduct a direct head-to-head comparison of the biological characteristics of the two types of MSCs under human platelet lysate-supplemented culture conditions for their ability to be used in regenerative medicine applications.

methodsThe bone marrow- and adipose tissue-derived MSCs were cultured under human platelet lysate conditions and their biological characteristics evaluated for cell therapy (morphology, immunophenotype, colony-forming unit-fibroblast efficiency, proliferation capacity, potential for mesodermal differentiation, secreted proteins, and immunomodulatory effects).

resultsUnder human platelet lysate-supplemented culture conditions, bone marrow- and adipose tissue-derived MSCs exhibited similar fibroblast-like morphology and expression patterns of surface markers. Adipose tissue-derived MSCs had greater proliferative potential than bone marrow-derived MSCs, while no significantly difference in colony efficiency were observed between the two types of cells. However, bone marrow-derived MSCs possessed higher capacity toward osteogenic and chondrogenic differentiation compared with adipose tissue-derived MSCs, while similar adipogenic differentiation potential wase observed between the two types of cells. There were some differences between bone marrow- and adipose tissue-derived MSCs for several secreted proteins, such as cytokine (interferon-γ), growth factors (basic fibroblast growth factor, hepatocyte growth factor, and insulin-like growth factor-1), and chemokine (stem cell-derived factor-1). Adipose tissue-derived MSCs had more potent immunomodulatory effects than bone marrow-derived MSCs.

conclusionsAdipose tissue-derived MSCs have biological advantages in the proliferative capacity, secreted proteins (basic fibroblast growth factor, interferon-γ, and insulin-like growth factor-1), and immunomodulatory effects, but bone marrow-derived MSCs have advantages in osteogenic and chondrogenic differentiation potential and secreted proteins (stem cell-derived factor-1 and hepatocyte growth factor); these biological advantages should be considered systematically when choosing the MSC source for specific clinical application.

Indexed as

Adipose TissueAntigens, CDBlood PlateletsBone Marrow CellsCell- and Tissue-Based TherapyCell DifferentiationCell ProliferationCells, CulturedChemokine CXCL12CytokinesEnzyme-Linked Immunosorbent AssayFibroblast Growth Factor 2Hepatocyte Growth FactorHumansImmunophenotypingInsulin-Like Growth Factor IAntigens, CDChemokine CXCL12CytokinesFibroblast Growth Factor 2Hepatocyte Growth FactorInsulin-Like Growth Factor I

Identifiers

PMID25884704
PMCPMC4453294

What OpenQuestion holds

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Registered trials

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.