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©The Author(s) 2025.
World J Stem Cells. Dec 26, 2025; 17(12): 114170
Published online Dec 26, 2025. doi: 10.4252/wjsc.v17.i12.114170
Table 4 Comparison of stromal vascular fraction and adipose-derived stem cells
Features
SVF
ASCs
DefinitionA heterogeneous cell mixture obtained directly from adipose tissue enzymatically or mechanically, comprising diverse stromal and immune cell populationsA relatively homogeneous mesenchymal stromal cell population derived from adherent culture and expansion of SVF
CompositionFibroblasts, endothelial cells, pericytes, smooth muscle cells, blood-derived cells, immune cells (T-cells, macrophages), and progenitor and stem cells (ASCs)Enriched in plastic-adherent multipotent MSCs with a fibroblast-like morphology, showing minimal hematopoietic contamination after passaging
HeterogeneityHighly heterogeneousRelatively homogeneous
MarkersCD34, CD45, CD31CD73, CD90, CD105
Isolation methodsSingle-step procedure following collagenase digestion or mechanical dissociation, without the need for culture or expansionRequires isolation from SVF followed by culture expansion over many days to weeks to enrich the adherent cell population
Mechanism of actionVascular/immune cells drive angiogenesis, immunomodulation, and tissue support, while ASCs contribute differentiationCombination of direct differentiation and strong paracrine effects (secretion of VEGF, HGF, IGF-1, extracellular vesicles)
Differentiation potentialVariable potential (due to cellular heterogeneity)Multilineage potential (adipogenic, osteogenic, chondrogenic)
Timeframe for useImmediate use application (cells can be reinjected within the same procedure)Not immediate use (requires laboratory processing and expansion)
Yield per gram of ATYields approximately 500000 to 2000000 nucleated cells per gram of fat but only 1%-10% are progenitors/stem cells[50]Yields approximately 5000-200000 ASCs per gram of fat after culture expansion depending on passages and technique[51]
ScalabilityConstrained by harvest volume and regulatory restrictions, as large-scale expansion is not feasible with same-day isolationsEasily scalable through in vitro expansion, allowing production of large cell doses from relatively small adipose samples
Clinical readinessUsed in autologous cell therapies (especially for cosmetic and orthopedic applications) as regulatory approval easier since it regarded as minimally manipulatedOngoing clinical trials in diverse fields (cardiovascular, musculoskeletal, inflammatory) as this requires GMP culture facilities
Key advantagesQuick, cost-effective, and maintains cellular diversityMore defined, reproducible, and expandable population
Current limitationsBatch variability, lower predictability of outcomes and regulatory debate on enzymatic methodsTime-consuming, cost-intensive, requires GMP conditions for clinical use


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