Evidence map›Paper›PMID 38551744›Full record

ArticleDigestive diseases and sciences2024

Deletion of Mixed Lineage Kinase Domain Like Pseudokinase Aggravates Chronic Alcohol-Induced Liver Injury via Increasing Apoptosis.

Keon Hwi Im, Waqar Khalid Saeed, Eun Bin Kim, A Hyeon Lee, Ji Eun Kim, Seung Min Lee, Xuanyuan Hanning, Hyun Sung Kim, Dae Won Jun, Eileen L Yoon

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Article in Digestive diseases and sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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10 authors at 3 institutions in 3 countries.

Keon Hwi Im *Department of Translational Medicine, Graduate School of Biomedical Science and Engineering, Hanyang University, 222 Wangsimni-Ro, Seongdong-Gu, Seoul, Republic of Korea.
Waqar Khalid Saeed *Department of Biomedical Sciences, Pak-Austria Fachhochschule: Institute of Applied Sciences and Technology, Mang, Haripur, Pakistan.
Eun Bin KimFaculty of Science, Bachelor of Medical Sciences, University of Western Ontario (ON), London, Canada.
A Hyeon LeeDepartment of Translational Medicine, Graduate School of Biomedical Science and Engineering, Hanyang University, 222 Wangsimni-Ro, Seongdong-Gu, Seoul, Republic of Korea.
Ji Eun KimDepartment of Translational Medicine, Graduate School of Biomedical Science and Engineering, Hanyang University, 222 Wangsimni-Ro, Seongdong-Gu, Seoul, Republic of Korea.
Seung Min LeeDepartment of Translational Medicine, Graduate School of Biomedical Science and Engineering, Hanyang University, 222 Wangsimni-Ro, Seongdong-Gu, Seoul, Republic of Korea.
Xuanyuan HanningDepartment of Internal Medicine, Hanyang University College of Medicine, 222 Wangsimni-Ro, Seongdong-Gu, Seoul, 133-791, Republic of Korea.
Hyun Sung KimDepartment of Pathology, Hanyang University School of Medicine, 222 Wangsimni-Ro, Seongdong-Gu, Seoul, Republic of Korea.
Dae Won Jun *Department of Translational Medicine, Graduate School of Biomedical Science and Engineering, Hanyang University, 222 Wangsimni-Ro, Seongdong-Gu, Seoul, Republic of Korea. noshin@hanyang.ac.kr.ORCID http://orcid.org/0000-0002-2875-6139
Eileen L Yoon *Department of Internal Medicine, Hanyang University College of Medicine, 222 Wangsimni-Ro, Seongdong-Gu, Seoul, 133-791, Republic of Korea.
Hanyang University · KRPakistan Institute of Engineering and Applied Sciences · PKWestern University · CA

Funding

Korean Association for the Study of the Liver KASL2019-04Ministry of Science and ICT, South Korea RS-2021-DD121073
6 · The paper itself

Abstract

BACKGROUND AND

aimhe mixed lineage kinase domain like pseudokinase (MLKL) is known to play a protective role in non-alcoholic fatty liver disease (NAFLD) via inhibition of necroptosis pathway. However, the role of MLKL in alcoholic liver disease (ALD) is not yet clear.

methodC57BL/6N wild-type (WT) and MLKL-knockout (KO) mice (8-10 weeks old) were randomly divided into eight groups. To establish ALD model of different durations, ethanol (EtOH) was fed to WT and MLKL KO for 10 days, 4 weeks, and 8 weeks. The control group was fed with Lieber-DeCarli control diet for 8 weeks. Mortality, degree of hepatic inflammation, and steatosis were compared among the groups. Bulk mRNA transcriptome analysis was performed. Abundance of transcript and gene expressions were calculated based on read count or Transcript by Million (TPM) value.

resultsSurvival rate of MLKL KO mice compared to WT was similar until 4 weeks, but the survival of MLKL KO mice significantly decreased after 8 weeks in ALD model. There was no difference in degree of inflammation, steatosis, and NAS scores between EtOH-fed MLKL KO and EtOH-fed WT mice at 10 days. However, at 4 weeks and 8 weeks, the degree of hepatic steatosis, NAS, and inflammation were increased in MLKL KO mice. RNA transcriptome data showed that fatty acid synthesis, and lipogenesis, mitochondria, and apoptosis-related pathways were upregulated in EtOH-fed MLKL KO mice compared to EtOH-fed WT mice. Although hepatocyte apoptosis (BAX/BCL2 ratio, caspase-3, and TUNEL staining) increased after EtOH intake; however, apoptosis was more significantly increased in EtOH-fed MLKL KO mice compared to the WT group. At the same time, hepatic cFLIP was decreased in EtOH-fed MLKL KO mice compared to the WT group.

conclusionMLKL deletion did not prevent chronic alcohol-induced liver damage independently of necroptosis and exacerbated hepatic steatosis by increasing hepatocyte apoptosis.

Indexed as

ApoptosisLiver Diseases, AlcoholicProtein KinasesAnimalsDisease Models, AnimalEthanolLiverMiceMice, Inbred C57BLMice, KnockoutEthanolMLKL protein, mouseProtein Kinases

Identifiers

PMID38551744
OpenAlexW4393314591

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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.