Evidence map›Paper›PMID 39334020›Full record

ArticleBMC pulmonary medicine2024

Mitochondrial transplantation attenuates lipopolysaccharide-induced acute respiratory distress syndrome.

Seo-Eun Lee, In-Hyeon Kim, Young Cheol Kang, Yujin Kim, Shin-Hye Yu, Jeong Seon Yeo, Iksun Kwon, Jun Hyeok Lim, Je-Hein Kim, Kyuboem Han and 2 more

Abstract read
In one paragraph

Article in BMC pulmonary medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 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.

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

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. 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

12 authors.

Seo-Eun Lee *Paean Biotechnology, Inc. 5 Samil-daero8-gil, Jung-gu, Seoul, 04552, Korea.
In-Hyeon Kim *Jeonbuk Branch Institute, Korea Institute of Toxicology, Jeongeup, 56212, Korea.
Young Cheol Kang *Paean Biotechnology, Inc. 5 Samil-daero8-gil, Jung-gu, Seoul, 04552, Korea.
Yujin KimPaean Biotechnology, Inc. 5 Samil-daero8-gil, Jung-gu, Seoul, 04552, Korea.
Shin-Hye YuPaean Biotechnology, Inc. 5 Samil-daero8-gil, Jung-gu, Seoul, 04552, Korea.
Jeong Seon YeoPaean Biotechnology, Inc. 5 Samil-daero8-gil, Jung-gu, Seoul, 04552, Korea.
Iksun KwonPaean Biotechnology, Inc. 5 Samil-daero8-gil, Jung-gu, Seoul, 04552, Korea.
Jun Hyeok LimPaean Biotechnology, Inc. 5 Samil-daero8-gil, Jung-gu, Seoul, 04552, Korea.
Je-Hein KimJeonbuk Branch Institute, Korea Institute of Toxicology, Jeongeup, 56212, Korea.
Kyuboem HanPaean Biotechnology, Inc. 5 Samil-daero8-gil, Jung-gu, Seoul, 04552, Korea.
Sung-Hwan KimJeonbuk Branch Institute, Korea Institute of Toxicology, Jeongeup, 56212, Korea. sunghwan.kim@kitox.re.kr.
Chun-Hyung KimPaean Biotechnology, Inc. 5 Samil-daero8-gil, Jung-gu, Seoul, 04552, Korea. chkim@paeanbio.com.

Funding

Industry-University-Research Institute platform cooperation R&D funded Korea Ministry of SMEs and Startups S3311100the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education NRF-2022R1A2C2006061
6 · The paper itself

Abstract

backgroundThe mitochondria are essential organelles not only providing cellular energy in the form of ATP, but also regulating the inflammatory response and the cell death program. Mitochondrial dysfunction has been associated with various human diseases, including metabolic syndromes as well as inflammatory and neurodegenerative diseases. Acute respiratory distress syndrome (ARDS) is an acute pulmonary disorder characterized by uncontrolled alveolar inflammation, apoptotic lung epithelial/endothelial cells, and pulmonary edema. Despite the high mortality of ARDS, an effective pharmacotherapy to treat this disease has not been established yet. Therefore, identifying a novel targeted therapy for ARDS is important. Recently, exogenous mitochondrial transplantation was reported to be beneficial for treating mitochondrial dysfunction. The current study aimed to investigate the therapeutic effect of mitochondrial transplantation on ARDS in vitro and in vivo.

methodsMitochondria were isolated from human stem cells. For in vitro efficacy of mitochondrial transplantation on the inflammation and cell death, murine alveolar macrophages MH-S and human pulmonary microvascular endothelial cells HPMECs were exposed to LPS, respectively. The ARDS mice model established by a single intratracheal instillation of LPS was used for in vivo efficacy of intravenously treated mitochondria.

resultsOur results showed that the mitochondria isolated from human stem cells exhibited an anti-inflammatory effect against alveolar macrophages and an anti-apoptotic effect against the alveolar epithelial cells. Furthermore, intravenous mitochondrial treatment was associated with the attenuation of lung injury in the LPS-induced ARDS mice.

conclusionDual effects of mitochondria on anti-inflammation and anti-apoptosis support the potential of mitochondrial transplantation as a novel therapeutic strategy for ARDS.

Indexed as

ApoptosisDisease Models, AnimalLipopolysaccharidesMitochondriaRespiratory Distress SyndromeAnimalsEndothelial CellsHumansMacrophages, AlveolarMaleMiceMice, Inbred C57BLLipopolysaccharidesAcute respiratory distress syndrome (ARDS)AntiapoptosisAnti-inflammationLipopolysaccharideMitochondriaStem cellTransplantation

Identifiers

PMID39334020
PMCPMC11437886

What Socratic 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 Socratic graph.