Role of Long Intergenic Nonprotein-Coding RNA 00511 in Nod-Like Receptor Protein Pyrin Domain 3-Induced Chondrocyte Pyroptosis via the MicroRNA-9-5p/FUT1 Axis
Tianjun Zhai, Zengqiao Zhang, Xiaoshen Hu, Dongyi He, Wei Feng

TL;DR
This study shows how a non-coding RNA, LINC00511, promotes chondrocyte cell death through a specific pathway involving miR-9-5p and FUT1.
Contribution
The study identifies a novel regulatory mechanism involving LINC00511, miR-9-5p, and FUT1 in chondrocyte pyroptosis.
Findings
LINC00511 silencing reduced NLRP3 inflammasome activity and chondrocyte pyroptosis.
LINC00511 acts as a sponge for miR-9-5p, which targets FUT1 to regulate pyroptosis.
Downregulating miR-9-5p or overexpressing FUT1 reversed the effects of LINC00511 silencing.
Abstract
This study aimed to determine the function of LINC00511 in Nod-Like Receptor Pyrin Domain 3 inflammasome-mediated chondrocyte pyroptosis via the regulation of miR-9-5p and FUT 1. Chondrocyte inflammatory injury was induced by treating chondrocytes with LPS. Afterwards, the levels of IL-1β and IL-18, the expression of NLRP3, ASC, Caspase-1, and GSDMD, cell viability, and LDH activity in chondrocytes were assessed. LINC00511 expression in LPS-treated chondrocytes was detected, and LINC00511 was subsequently silenced to analyse its role in chondrocyte pyroptosis. The subcellular localization of LINC00511 was predicted and verified. Furthermore, the binding relationships between LINC00511 and miR-9-5p and between miR-9-5p and FUT1 were validated. LINC00511 regulated NLRP3 inflammasome-mediated chondrocyte pyroptosis through the miR-9-5p/FUT1 axis. LPS-treated ATDC5 cells exhibited elevated…
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Taxonomy
TopicsInflammasome and immune disorders · Cancer-related molecular mechanisms research · Osteoarthritis Treatment and Mechanisms
