2021
DOI: 10.1002/2211-5463.13049
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Reduced RING finger protein 10 expression in macrophages is associated with aging‐related inflammation

Abstract: The understanding of the mechanism governing the onset of immunosenescence remains incomplete. Here, we found that RNF10 could be suppressed by increased TLR‐TRIF pathway activation and maintained at a low level in aged macrophages compared with young cells. Moreover, reduced RNF10 increased lipopolysaccharide‐triggered signaling pathways of nuclear factor‐κB and interferon regulatory factor 3, thereby enhancing proinflammatory cytokines and interferons in aged cells.

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Cited by 3 publications
(1 citation statement)
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“…Cardiomyocytes are important sites of RNF10 expression [16,33]. When the myocardium is damaged, the expression and transcription of RNF10 in the myocardial UPS system are affected, resulting in the production and degradation of a large number of signal proteins, which directly affect cardiac energy metabolism, the inflammatory response, oxidative stress, and apoptotic autophagy [17,21,22,34]. The key is that RNF10 can target and regulate the expression of AP-1 and Meox2 [17,[20][21][22].…”
Section: Discussionmentioning
confidence: 99%
“…Cardiomyocytes are important sites of RNF10 expression [16,33]. When the myocardium is damaged, the expression and transcription of RNF10 in the myocardial UPS system are affected, resulting in the production and degradation of a large number of signal proteins, which directly affect cardiac energy metabolism, the inflammatory response, oxidative stress, and apoptotic autophagy [17,21,22,34]. The key is that RNF10 can target and regulate the expression of AP-1 and Meox2 [17,[20][21][22].…”
Section: Discussionmentioning
confidence: 99%