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Characterization and functional analysis of the adipose tissue-derived stromal vascular fraction of pediatric patients with osteogenesis imperfecta. | LitMetric

AI Article Synopsis

  • * A new study explored using the stromal vascular fraction (SVF) from adipose tissue as a less invasive and potentially abundant alternative to traditional bone-marrow-derived stem cells for bone regeneration in OI patients.
  • * The research found that both OI patients and non-OI controls had similar viable cell counts in the isolated SVF, and these cells demonstrated the ability to differentiate into various cell types (cartilage, fat, bone) in a lab setting, suggesting SVF could be effectively

Article Abstract

Pediatric patients with Osteogenesis Imperfecta (OI), a heritable connective tissue disorder, frequently suffer from long bone deformations. Surgical correction often results in bone non-unions, necessitating revision surgery with autogenous bone grafting using bone-marrow-derived stem cells (BM-SC) to regenerate bone. BM-SC harvest is generally invasive and limited in supply; thus, adipose tissue's stromal vascular fraction (SVF) has been introduced as an alternative stem cell reservoir. To elucidate if OI patients' surgical site dissected adipose tissue could be used as autologous bone graft in future, we investigated whether the underlying genetic condition alters SVF's cell populations and in vitro differentiation capacity. After optimizing SVF isolation, we demonstrate successful isolation of SVF of pediatric OI patients and non-OI controls. The number of viable cells was comparable between OI and controls, with about 450,000 per gram tissue. Age, sex, type of OI, disease-causing collagen mutation, or anatomical site of harvest did not affect cell outcome. Further, SVF-containing cell populations were similar between OI and controls, and all isolated SVF's demonstrated chondrogenic, adipogenic, and osteogenic differentiation capacity in vitro. These results indicate that SVF from pediatric OI patients could be used as a source of stem cells for autologous stem cell therapy in OI.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844034PMC
http://dx.doi.org/10.1038/s41598-022-06063-4DOI Listing

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