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源自间充质干细胞(MSCs)的细胞外囊泡(EVs)作为慢性肾脏病(CKD)治疗中的佐剂

Extracellular Vesicles (EVs) Derived from Mesenchymal Stem Cells (MSCs) as Adjuvants in the Treatment of Chronic Kidney Disease (CKD).

作者信息

Noda Paloma, Francini Ana L R, Teles Flavio, Júnior Samuel J, Fonseca Fernando L A, Borges Fernanda T, Sobrinho Adão C, Taniwaki Noemi, Noronha Irene L, Fanelli Camilla

机构信息

Laboratory of Cellular, Genetic and Molecular Nephrology, Renal Division, Faculty of Medicine, University of São Paulo, Av. Dr. Arnaldo, 455, 4° Andar, 4304, São Paulo 01246-903, SP, Brazil.

Renal Division, Faculty of Medicine, Federal University of Alagoas, Maceio 57200-000, AL, Brazil.

出版信息

Cells. 2025 Mar 14;14(6):434. doi: 10.3390/cells14060434.

Abstract

Chronic kidney disease (CKD) is considered an important health issue worldwide. The renin-angiotensin-aldosterone system (RAAS) blockade through the administration of angiotensin II receptor blockers, such as Losartan (LOS), has been considered the best strategy for CKD treatment for decades. However, this approach promotes only partial detention of CKD progression and cannot reverse renal damage. The aim of the present study was to investigate whether the therapeutic administration of extracellular vesicles (EVs) derived from adipose stem cells (ASCs), associated to LOS treatment, would promote additional renoprotection in rats underwent the 5/6 renal ablation CKD model. ASC-derived EV were administered locally, in the renal subcapsular area, 15 days after CKD induction, when LOS therapy also began. Animals were followed for additional 15 days and our results demonstrated that subcapsular injection of ASC-derived EV associated with LOS significantly reduced glomerulosclerosis, renal interstitial infiltration by myofibroblasts, and macrophages in the 5/6 CKD model. Additionally, LOS + EV abrogated systemic hypertension, proteinuria, and albuminuria, and stimulated local gene overexpression of the endogenous anti-inflammatory . Although more studies are still required to establish the best EV dose and administration route, these findings point to therapy with ASC-derived EV as a potential adjuvant in CKD treatment.

摘要

慢性肾脏病(CKD)被认为是全球重要的健康问题。几十年来,通过给予血管紧张素II受体阻滞剂(如氯沙坦,LOS)来阻断肾素-血管紧张素-醛固酮系统(RAAS),一直被视为CKD治疗的最佳策略。然而,这种方法仅能部分延缓CKD进展,无法逆转肾损伤。本研究的目的是探究在接受5/6肾切除CKD模型的大鼠中,与LOS治疗联合应用的脂肪干细胞(ASC)来源的细胞外囊泡(EV)进行治疗性给药,是否会促进额外的肾脏保护作用。在CKD诱导15天后,当LOS治疗也开始时,将ASC来源的EV局部注射到肾被膜下区域。对动物再随访15天,我们的结果表明,在5/6 CKD模型中,与LOS联合的肾被膜下注射ASC来源的EV显著降低了肾小球硬化、肌成纤维细胞和巨噬细胞的肾间质浸润。此外,LOS + EV消除了系统性高血压、蛋白尿和白蛋白尿,并刺激了内源性抗炎因子的局部基因过表达。尽管仍需要更多研究来确定最佳的EV剂量和给药途径,但这些发现表明ASC来源的EV治疗作为CKD治疗的潜在辅助手段。

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