[Culture of the single cell clones of human adipose-derived stem cells and identification of their surface antigen expressions].
Gu F., Gao JH., Lu F.
Laboratory Study on Face & Skin, published in Nan Fang Yi Ke Da Xue Xue Bao (2008) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.
- Study type
- Laboratory Study
- Journal
- Nan Fang Yi Ke Da Xue Xue Bao (2008)
- Country
- China
- Reported sample size
- —
- Source database
- PubMed
- PMID
- 18583266
- Citations
- 1
Abstract (original English)
Objective To perform single cell clone culture of human adipose-derived stem cells (hASCs), and identify their surface antigens in different clones. Methods Surgically removed human adipose tissues were digested with collagenase to isolate hASCs, which were seeded in primary culture. After culture to the second passage, the hASCs were committed to limiting dilution assays to form the colony units. Each of the clones obtained were examined with flow cytometry to identify the expressions of cell-surface antigens including CD29, CD44, CD34, CD54, CD106, and ABCG2. Results Ten clones were obtained by colony-forming unit (CFU) assays, and after culture to the 9th passage, a portion of the cells were frozen in liquid nitrogen. All the clones exhibited similar fibroblast-like morphology, but their proliferative activities varied. Flow cytometry showed that all the clones were strongly positive for CD29 and CD44 but with rather low ABCG2 expression. The expressions of CD34, CD54 and CD106 varied between the cell clones. Conclusion hASCs harvested from human adipose tissue with collagenase digestion represent a hybrid population of multilineage stem cells. CFU assays may result in single purified hASC clones, and the different clones differ in but also share some common surface antigens, possibly due to their different potentials of differentiation.
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is preclinical work; animal or laboratory results cannot be applied to humans.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
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