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

被引:1
作者
Noda, Paloma [1 ]
Francini, Ana L. R. [1 ]
Teles, Flavio [2 ]
Junior, Samuel J. [1 ]
Fonseca, Fernando L. A. [3 ]
Borges, Fernanda T. [4 ]
Sobrinho, Adao C. [5 ]
Taniwaki, Noemi [6 ]
Noronha, Irene L. [1 ]
Fanelli, Camilla [1 ]
机构
[1] Univ Sao Paulo, Fac Med, Renal Div, Lab Cellular Genet & Mol Nephrol, Av Dr Arnaldo 455,4 Andar, BR-01246903 Sao Paulo, SP, Brazil
[2] Univ Fed Alagoas, Fac Med, Renal Div, BR-57200000 Maceio, AL, Brazil
[3] Univ Ctr ABC Med Sch, Dept Clin Lab, BR-09060650 Santo Andre, SP, Brazil
[4] Univ Fed Sao Paulo, Paulista Sch Med, Dept Med, Nephrol Div, BR-04023062 Sao Paulo, SP, Brazil
[5] Univ Sao Paulo, Sch Med, Dept Pathol, Lab Cellular Biol, BR-01246903 Sao Paulo, SP, Brazil
[6] Adolfo Lutz Inst, Lab Electron Microscopy, BR-01246000 Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
extracellular vesicles; chronic kidney disease; cell therapy; mesenchymal stem cells; RENAL-DISEASE; LOSARTAN; INJURY;
D O I
10.3390/cells14060434
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 Il-4. 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
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页数:22
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