Evidence map›Paper›PMID 38570846›Full record

ArticleJournal of nanobiotechnology2024

Hyaluronic acid stimulation of stem cells for cardiac repair: a cell-free strategy for myocardial infarct.

Seon-Yeong Jeong, Bong-Woo Park, Jimin Kim, Seulki Lee, Haedeun You, Joohyun Lee, Susie Lee, Jae-Hyun Park, Jinju Kim, Woosup Sim and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
8.6field-weighted citation impact, top 2% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

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  10. Genetic factors in the pathogenesis of cardio-oncology.Journal of translational medicine · 2024
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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

14 authors at 2 institutions in 2 countries.

Seon-Yeong Jeong *Brexogen Research Center, Brexogen Inc., Songpa‑gu, Seoul, 05855, South Korea.
Bong-Woo Park *Department of Biomedicine & Health Sciences, The Catholic University of Korea, 222 Banpo-daero, Seoho-gu, Seoul, 06591, Republic of Korea.
Jimin KimBrexogen Research Center, Brexogen Inc., Songpa‑gu, Seoul, 05855, South Korea.
Seulki LeeBrexogen Research Center, Brexogen Inc., Songpa‑gu, Seoul, 05855, South Korea.
Haedeun YouBrexogen Research Center, Brexogen Inc., Songpa‑gu, Seoul, 05855, South Korea.
Joohyun LeeBrexogen Research Center, Brexogen Inc., Songpa‑gu, Seoul, 05855, South Korea.
Susie LeeDepartment of Biomedicine & Health Sciences, The Catholic University of Korea, 222 Banpo-daero, Seoho-gu, Seoul, 06591, Republic of Korea.
Jae-Hyun ParkDepartment of Biomedicine & Health Sciences, The Catholic University of Korea, 222 Banpo-daero, Seoho-gu, Seoul, 06591, Republic of Korea.
Jinju KimDepartment of Biomedicine & Health Sciences, The Catholic University of Korea, 222 Banpo-daero, Seoho-gu, Seoul, 06591, Republic of Korea.
Woosup SimDepartment of Biomedicine & Health Sciences, The Catholic University of Korea, 222 Banpo-daero, Seoho-gu, Seoul, 06591, Republic of Korea.
Kiwon BanDepartment of Biomedical Science, City University of Hong Kong, Kowloon Tong, Hong Kong.
Joonghoon ParkGraduate School of International Agricultural Technology, Institutes of Green-Bio Science and Technology, Seoul National University, Pyeongchang, Gangwon-do, 25354, South Korea.
Hun-Jun ParkDepartment of Biomedicine & Health Sciences, The Catholic University of Korea, 222 Banpo-daero, Seoho-gu, Seoul, 06591, Republic of Korea. cardioman@catholic.ac.kr.
Soo KimBrexogen Research Center, Brexogen Inc., Songpa‑gu, Seoul, 05855, South Korea. sue.kim@brexogen.com.
Catholic University of Korea · KRCity University of Hong Kong · HK

Funding

Korean Fund for Regenerative Medicine funded by the Ministry of Science and ICT, the Ministry of Health and Welfare 21C0708L1-13National Research Foundation of Korea Grant funded by the Korean Government NRF-2022R1A2C2009067
6 · The paper itself

Abstract

backgroundMyocardial infarction (MI), a representative form of ischemic heart disease, remains a huge burden worldwide. This study aimed to explore whether extracellular vesicles (EVs) secreted from hyaluronic acid (HA)-primed induced mesenchymal stem cells (HA-iMSC-EVs) could enhance the cardiac repair after MI.

resultsHA-iMSC-EVs showed typical characteristics for EVs such as morphology, size, and marker proteins expression. Compared with iMSC-EVs, HA-iMSC-EVs showed enhanced tube formation and survival against oxidative stress in endothelial cells, while reduced reactive oxygen species (ROS) generation in cardiomyocytes. In THP-1 macrophages, both types of EVs markedly reduced the expression of pro-inflammatory signaling players, whereas HA-iMSC-EVs were more potent in augmenting anti-inflammatory markers. A significant decrease of inflammasome proteins was observed in HA-iMSC-EV-treated THP-1. Further, phospho-SMAD2 as well as fibrosis markers in TGF-β1-stimulated cardiomyocytes were reduced in HA-iMSC-EVs treatment. Proteomic data showed that HA-iMSC-EVs were enriched with multiple pathways including immunity, extracellular matrix organization, angiogenesis, and cell cycle. The localization of HA-iMSC-EVs in myocardium was confirmed after delivery by either intravenous or intramyocardial route, with the latter increased intensity. Echocardiography revealed that intramyocardial HA-iMSC-EVs injections improved cardiac function and reduced adverse cardiac remodeling and necrotic size in MI heart. Histologically, MI hearts receiving HA-iMSC-EVs had increased capillary density and viable myocardium, while showed reduced fibrosis.

conclusionsOur results suggest that HA-iMSC-EVs improve cardiac function by augmenting vessel growth, while reducing ROS generation, inflammation, and fibrosis in MI heart.

Indexed as

Mesenchymal Stem CellsMyocardial InfarctionEndothelial CellsFibrosisHumansHyaluronic AcidMyocytes, CardiacProteomicsReactive Oxygen SpeciesHyaluronic AcidReactive Oxygen SpeciesExtracellular vesiclesInduced Mesenchymal stem cellsMyocardial infarction

Identifiers

PMID38570846
PMCPMC10993512
OpenAlexW4393946571

What OpenQuestion 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 OpenQuestion graph.