Evidence map›Paper›PMID 31569434›Full record

ArticleInternational journal of molecular sciences2019

Enhancing the Wound Healing Effect of Conditioned Medium Collected from Mesenchymal Stem Cells with High Passage Number Using Bioreducible Nanoparticles.

Gwang-Bum Im, Yeong Hwan Kim, Yu-Jin Kim, Sung-Won Kim, Euiyoung Jung, Gun-Jae Jeong, Ke Wang, Jinheung Kim, Dong-Ik Kim, Tae-Hyung Kim and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  12. Stem Cell Therapy for Burns: Story so Far.Biologics : targets & therapy · 2021
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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

13 authors at 5 institutions in 1 country.

Gwang-Bum ImSchool of Chemical Engineering, Sungkyunkwan University, Suwon 16419, Korea. lki1005@skku.edu.
Yeong Hwan KimSchool of Chemical Engineering, Sungkyunkwan University, Suwon 16419, Korea. iva9110@gmail.com.
Yu-Jin KimSchool of Chemical Engineering, Sungkyunkwan University, Suwon 16419, Korea. yujinkim1003@gmail.com.
Sung-Won KimSchool of Chemical Engineering, Sungkyunkwan University, Suwon 16419, Korea. tjdnjdl90@skku.edu.
Euiyoung JungDepartment of Chemical Engineering, Kyung Hee University, Youngin 17104, Korea. jey9207@khu.ac.kr.
Gun-Jae JeongDivision of Vascular Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06351, Korea. jgj814@skku.edu.ORCID 0000-0002-0106-0078
Ke WangSchool of Chemical Engineering, Sungkyunkwan University, Suwon 16419, Korea. kewang@hust.edu.cn.
Jinheung KimDepartment of Chemistry and Nano Science, Ewha Womans University, Seoul 120-750, Korea. jinheung@ewha.ac.kr.
Dong-Ik KimDivision of Vascular Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06351, Korea. dikim@skku.edu.
Tae-Hyung KimSchool of Integrative Engineering, Chung-Ang University, Seoul 06974, Korea. thkim0512@cau.ac.kr.
Gi-Ra YiSchool of Chemical Engineering, Sungkyunkwan University, Suwon 16419, Korea. yigira@skku.edu.ORCID 0000-0003-1353-8988
Taekyung YuDepartment of Chemical Engineering, Kyung Hee University, Youngin 17104, Korea. tkyu@khu.ac.kr.
Suk Ho BhangSchool of Chemical Engineering, Sungkyunkwan University, Suwon 16419, Korea. sukhobhang@skku.edu.
Sungkyunkwan University · KREwha Womans University · KRSamsung Medical Center · KRChung-Ang University · KRKyung Hee University · KR

Funding

Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea grant HI17C1728Ministry of Science, ICT and Future Planning NRF-2016M3A9B4919711Ministry of Science, ICT and Future Planning NRF-2018M3A9E2023255, NRF-2017R1A5A1070259, NRF-2019R1C1C1007384NRF grant funded by the Korean government (MSIP) NRF-2014R1A5A1009799, NRF- 2019R1H1A22079332, and NRF-2016M3D1A1021140
6 · The paper itself

Abstract

Injecting human mesenchymal stem cells (hMSCs) at wound sites is known to have a therapeutic effect; however, hMSCs have several limitations, such as low viability and poor engraftment after injection, as well as a potential risk of oncogenesis. The use of a conditioned medium (CM) was suggested as an alternative method for treating various wounds instead of direct hMSC administration. In addition to not having the adverse effects associated with hMSCs, a CM can be easily mass produced and can be stored for long-term, thereby making it useful for clinical applications. In general, a CM is collected from hMSCs with low passage number; whereas, the hMSCs with high passage number are usually discarded because of their low therapeutic efficacy as a result of reduced angiogenic factor secretion. Herein, we used a CM collected from high passage number (passage 12, P12) hMSCs treated with gold-iron nanoparticles (AuFe NPs). Our AuFe NPs were designed to release the iron ion intracellularly via endocytosis. Endosomes with low pH can dissolve iron from AuFe NPs, and thus, the intracellularly released iron ions up-regulate the hypoxia-inducible factor 1α and vascular endothelial growth factor (VEGF) expression. Through this mechanism, AuFe NPs improve the amount of VEGF expression from P12 hMSCs so that it is comparable to the amount of VEGF expression from low passage number (passage 6, P6), without treatment. Furthermore, we injected the CM retrieved from P12 MSCs treated with AuFe NPs in the mouse skin wound model (AuFe P12 group). AuFe P12 group revealed significantly enhanced angiogenesis in the mouse skin wound model compared to the high passage hMSC CM-injected group. Moreover, the result from the AuFe P12 group was similar to that of the low passage hMSC CM-injected group. Both the AuFe P12 group and low passage hMSC CM-injected group presented significantly enhanced re-epithelization, angiogenesis, and tissue remodeling compared to the high passage hMSC CM-injected group. This study reveals a new strategy for tissue regeneration based on CM injection without considering the high cell passage count.

Indexed as

NanoparticlesBiocompatible MaterialsCell Culture TechniquesCell SurvivalCulture Media, ConditionedGene Expression RegulationHumansMesenchymal Stem CellsVascular Endothelial Growth Factor AWound HealingBiocompatible MaterialsCulture Media, ConditionedVascular Endothelial Growth Factor Aangiogenesishigh passagemesenchymal stem cellnanoparticle

Identifiers

PMID31569434
PMCPMC6801963
OpenAlexW2975767508

What Socratic 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 Socratic graph.