LAUSR

The adipose‐derived stromal vascular fraction (SVF) is composed of a heterogeneous mix of adipose‐derived stem cells (ADSCs), macrophages, pericytes, fibroblasts, blood, and other cells. Previous studies have found that the paracrine effects of SVF cells may be therapeutic, but their role in osteoarthritis treatment remains unclear. This study aimed to investigate the therapeutic effect of SVF cells on chondrocytes. Chondrocytes were seeded on culture plates alone (control) or cocultured with SVF or ADSCs on cell culture inserts. After 48 h of coculture, chondrocyte collagen II, tissue inhibitors of metalloproteinases‐3 (TIMP‐3), and matrix metalloproteinases‐13 (MMP‐13) messenger RNA (mRNA) expression levels were evaluated using reverse‐transcription polymerase chain reaction, and the transforming growth factor‐β (TGF‐β) levels in the supernatant were measured using ELISA. Immunohistochemical staining and flow cytometry were used to evaluate the macrophages in the SVF. These macrophages were characterized according to phenotype using the F4/80, CD86, and CD163 markers. To determine whether the Smad2/3 signaling pathways were involved, the chondrocytes were pre‑treated with a Smad2/3 phosphorylation inhibitor and stimulated with the SVF, and then Smad2/3 phosphorylation levels were analyzed using western blot. The mRNA expression levels of various paracrine factors and chondrocyte pellet size were also assessed. Collagen II and TIMP‐3 expression were higher in the SVF group than in the ADSC group and controls, while MMP‐13 expression was the highest in the ADSC group and the lowest in the controls. TGF‐β levels in the SVF group were also elevated. Immunohistochemical staining and flow cytometry revealed that the macrophages in the SVF were of the anti‐inflammatory phenotype. Western blot analysis showed that the SVF increased Smad2/3 phosphorylation, while Smad2/3 inhibitors decreased phosphorylation. Smad2/3 inhibitors also reduced the expression of various other paracrine factors and decreased chondrocyte pellet size. These findings suggested that the paracrine effect of heterogeneous cells, such as anti‐inflammatory macrophages, in the SVF partly supports chondrocyte regeneration through TGF‐β‐induced Smad2/3 phosphorylation.