2022
DOI: 10.26508/lsa.202201468
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circEXOC5 promotes acute lung injury through the PTBP1/Skp2/Runx2 axis to activate autophagy

Abstract: To understand the pathogenesis of acute lung injury (ALI), we focused on circEXOC5, a significantly up-regulated circular RNA in ALI. Using the in vivo cecal ligation and puncture (CLP)–induced ALI mouse model and in vitro LPS-challenged mouse pulmonary microvascular endothelial cell (MPVEC) model, we examined the impacts of knockdown circEXOC5 on lung injury, inflammation, and autophagy. The regulation between circEXOC5, polypyrimidine tract-binding protein 1 (PTBP1), S-phase kinase-associated protein 2 (Skp2… Show more

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Cited by 8 publications
(4 citation statements)
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“…It is required for photoreceptor ciliogenesis and retinal development [ 40 ]. A recent work demonstrated that circEXOC5 (hsa_circ_0004399) is one of the mostly significantly up regulated circRNAs identified by microarray in lung macrophages from acute lung injured mice compared to control mice finally demonstrating a pivotal role of this circRNAs in promoting acute lung injury in mice [ 41 ].…”
Section: Discussionmentioning
confidence: 99%
“…It is required for photoreceptor ciliogenesis and retinal development [ 40 ]. A recent work demonstrated that circEXOC5 (hsa_circ_0004399) is one of the mostly significantly up regulated circRNAs identified by microarray in lung macrophages from acute lung injured mice compared to control mice finally demonstrating a pivotal role of this circRNAs in promoting acute lung injury in mice [ 41 ].…”
Section: Discussionmentioning
confidence: 99%
“…We cut the PVDF membrane while retaining sufficient width and length to allow different positions of the PVDF membrane to bond with different primary antibodies. Then blotted with primary antibodies for LC3 (1:1000, ab192890, Abcam) 54 , P62 (1:1000, ab109012, Abcam) 55 , SIRT3 (1:500, #5490, CST) 56 , SOD2 (1:1000, #13141, CST) 57 , acetylated SOD2 (1:1000, ab137037, Abcam) 58 and GAPDH (1:2000, 60004-1-Ig, Proteintech) 59 overnight at 4 °C. Then, incubate with the secondary antibody for 1.5 h at room temperature.…”
Section: Methodsmentioning
confidence: 99%
“…So far, there have been a few studies focusing on the detection of either ALP or RUNX2 with the help of graphene-based biosensors. Mahato et al [34] developed an impedimetric biosensor using gold-nano-dendroids and graphene oxide (GO) detecting ALP in human serum samples, Liu et al [35] describe a fluorescent assay based on GO and λ exonuclease for ALP activity, while to the best of our knowledge, RUNX2 detection is still performed using classical techniques like quantitative PCR (qPCR) [36], Western blot [37], and immunohistochemistry [38], while no progress has been made regarding the development of a novel electrochemical biosensor to detect this biomarker. Ma'arif et al [22] compared two techniques used for RUNX2 detection in bone tissue, i.e., Western blot and immunohistochemistry, investigating 70 articles, and concluded that the Western blot method is superior in terms of sensitivity, selectivity, cost, and detection time.…”
Section: Introductionmentioning
confidence: 99%