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Updated: May 11, 2026

Manual Isolation of Adipose-derived Stem Cells from Human Lipoaspirates
Published on: September 26, 2013
Adipose Tissue Stem Cells (ASCs) and ASC-Derived Extracellular Vesicles Prevent the Development of Experimental
Priscila Q Gouveia1, Camilla Fanelli1, Felipe M Ornellas1
1Laboratory of Cellular, Genetic, and Molecular Nephrology, Renal Division, Medical School, University of São Paulo, São Paulo 01246-903, Brazil.
Adipose-tissue-derived stem cells (ASCs) and extracellular vesicles (EVs) show promise in treating peritoneal fibrosis (PF). Both therapies reduced fibrosis markers and inflammation, with EVs offering superior preservation of peritoneal membrane function and ultrafiltration capacity.
Area of Science:
- Regenerative Medicine
- Cell Therapy
- Biomaterials Science
Background:
- Peritoneal fibrosis (PF) is a serious complication of peritoneal dialysis, potentially leading to peritoneal membrane failure.
- Mesenchymal stromal cells (MSCs) offer therapeutic potential via paracrine mechanisms for regenerative applications.
- Protecting the peritoneal membrane (PM) is crucial for patients undergoing peritoneal dialysis.
Purpose of the Study:
- To investigate the efficacy of adipose-tissue-derived stem cells (ASCs) and extracellular vesicles (EVs) in mitigating peritoneal fibrosis (PF).
- To evaluate the impact of ASCs and EVs on peritoneal membrane structure, fibrosis markers, inflammation, and function in a rat model.
Main Methods:
- A rat model of peritoneal fibrosis (PF) was induced using chlorhexidine gluconate.
- Animals were treated with ASCs or EVs to assess their therapeutic effects.
- Key markers of fibrosis, inflammation, gene expression (Smad3, Smad7), and peritoneal membrane function (ultrafiltration capacity, glucose transport, neoangiogenesis) were analyzed.
Main Results:
- ASC and EV treatments significantly prevented PM thickening and reduced myofibroblasts, fibronectin, collagen III, TGF-β, and FSP-1.
- Both treatments exhibited potent anti-inflammatory effects and modulated Smad3/Smad7 gene expression.
- While VEGF expression decreased, peritoneal function remained effective, with EVs showing superior enhancement of ultrafiltration capacity.
Conclusions:
- ASCs and EVs effectively hinder PF progression and exert anti-inflammatory effects in an experimental model.
- EV treatment demonstrated superior preservation of peritoneal membrane function and enhanced ultrafiltration capacity.
- ASCs and EVs represent promising novel therapeutic strategies for preventing peritoneal dialysis-associated PF.
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