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mTORC1 activation on membranes We used large unilamellar vesicles (LUVs), with a lipid composition of 72.8% DOPC, 7% POPS, 10% cholesterol, 5% DGS-nitrilotriacetic acid (NTA), 5% PE MCC and 0.2% DiR, as the membrane platform to investigate the role of RAGRagulator and RHEB in mTORC1 activation

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4.2 Potential impact of gut microbiota on ferroptosis in OA 4.2.1 Gut dysbiosis promotes lipid peroxidation and ferroptosis in OA In patients with OA, the significant dysregulation of the gut microbiota not only manifests as a disorder in the community structure but also profoundly affects the pathological process of OA by precisely regulating the key hub genes in the host lipid metabolism network

Although existing studies indicate that MT has the potential to improve energy metabolism, reduce cell death, modulate inflammatory responses, and promote tissue regeneration, the specific molecular mechanisms and signaling pathways require further investigation