Claudio Ponticelli, Gabriella Moroni
, Via Ampere 126, Milan, Italy.
Department of Biomedical Sciences, Humanitas University, Via Rita Levi Montalcini 4 Pieve Emanuele, 20072, Milan, Italy.
J Nephrol. 2025 Mar 19. doi: 10.1007/s40620-025-02267-9.
Autophagy is a natural process whereby damaged or dying parts of a cell are eliminated and recycled. The term autophagy usually refers to macroautophagy, which is one of three types of autophagy, alongside microautophagy and chaperone-mediated autophagy. Autophagy is activated by adenosine monophosphate-activated protein kinase (AMPK) and inhibited by mammalian target of rapamycin (mTOR) through their interference with Unc-51-like kinase 1 (ULK1). Dysregulated autophagy is deeply involved in autoimmune glomerular diseases. Upregulated autophagy can induce inflammation and activate innate and adaptive immunity. However, autophagy may also exert a protective role on podocytes, enhance endothelial cell function, and preserve proximal tubular epithelial cells during ischemic or endotoxic acute kidney injury (AKI). Hydroxychloroquine (HCQ) can downregulate increased autophagy and is widely used in lupus nephritis. HCQ causes alkalinization, which results in vacuolization of lysosomes and inhibition of their functions. By inhibiting autophagic activity, HCQ may reduce inflammation and innate immunity, inhibit the activation of T cells, restore the T helper 17/T regulator balance, restrict the production of pro-inflammatory cytokines, and modulate co-stimulatory molecules. This reduces the risk of flares, spares the dosage of glucocorticoids, improves lupus activity, and prevents the thrombotic effects of anti-phospholipid antibodies. Recent studies showed that HCQ can also reduce proteinuria in IgA nephropathy (IgAN) and membranous nephropathy (MN). Drugs that improve mitochondrial function or enhance autophagy, such as metformin, sodium-glucose co-transporter 2 (SGLT2) inhibitors or mTOR inhibitors, may exert protective effects on podocytes and reduce proteinuria in MN or focal segmental glomerulosclerosis (FSGS).
自噬是一种自然过程,通过该过程细胞受损或即将死亡的部分被清除并循环利用。术语“自噬”通常指巨自噬,它是自噬的三种类型之一,另外两种是微自噬和伴侣介导的自噬。自噬由单磷酸腺苷激活的蛋白激酶(AMPK)激活,并通过其对Unc-51样激酶1(ULK1)的干扰被雷帕霉素哺乳动物靶蛋白(mTOR)抑制。自噬失调与自身免疫性肾小球疾病密切相关。自噬上调可诱导炎症并激活先天性和适应性免疫。然而,自噬在足细胞中也可能发挥保护作用,增强内皮细胞功能,并在缺血性或内毒素性急性肾损伤(AKI)期间保护近端肾小管上皮细胞。羟氯喹(HCQ)可下调增加的自噬,并且广泛用于狼疮性肾炎。HCQ导致碱化,这会导致溶酶体空泡化并抑制其功能。通过抑制自噬活性,HCQ可减少炎症和先天性免疫,抑制T细胞的激活,恢复辅助性T细胞17/调节性T细胞平衡,限制促炎细胞因子的产生,并调节共刺激分子。这降低了疾病发作的风险,节省了糖皮质激素的用量,改善了狼疮活动,并防止了抗磷脂抗体的血栓形成作用。最近的研究表明,HCQ还可以降低IgA肾病(IgAN)和膜性肾病(MN)中的蛋白尿。改善线粒体功能或增强自噬的药物,如二甲双胍、钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂或mTOR抑制剂,可能对足细胞发挥保护作用,并减少MN或局灶节段性肾小球硬化(FSGS)中的蛋白尿。