Your browser doesn't support javascript.
loading
Micronized cellular adipose matrix purified with a bladed connector contains abundant functional adipose stem cells.
Sowa, Yoshihiro; Sawai, Seiji; Yamamoto, Kenta; Sunaga, Ataru; Saito, Natsumi; Shirado, Takako; Toyohara, Yoshihiro; Bolun, Li; Yoshimura, Kotaro; Mazda, Osam.
Affiliation
  • Sowa Y; Department of Plastic Surgery, Jichi Medical University, Japan; Department of Immunology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan; Department of Plastic and Reconstructive Surgery, Graduate School of Medical Science, Kyoto Prefectural University of
  • Sawai S; Department of Immunology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Yamamoto K; Department of Immunology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Sunaga A; Department of Plastic Surgery, Jichi Medical University, Japan.
  • Saito N; Department of Plastic Surgery, Jichi Medical University, Japan.
  • Shirado T; Department of Plastic Surgery, Jichi Medical University, Japan.
  • Toyohara Y; Department of Plastic Surgery, Jichi Medical University, Japan.
  • Bolun L; Department of Plastic Surgery, Jichi Medical University, Japan.
  • Yoshimura K; Department of Plastic Surgery, Jichi Medical University, Japan.
  • Mazda O; Department of Immunology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Tissue Cell ; 89: 102457, 2024 Aug.
Article in En | MEDLINE | ID: mdl-38996772
ABSTRACT

INTRODUCTION:

A specialized device equipped with a sharp blade filter has been developed to enable more efficient purification of a micronized cellular adipose matrix (MCAM) containing stem cells. The aim of this study is to compare the characteristics and functions of the population of stromal cells (mSVF) and cultured cells (mASCs) purified using this device with those of cSVF and cASCs obtained through conventional enzymatic purification.

METHODS:

Cell viability, proliferation capacity and yield were assessed. Characterization of stem cell potency was performed by analyzing cell surface markers including CD34, a marker of activated adipose-derived stem cells. The trilineage differentiation potential was evaluated using RT-PCR and histology.

RESULTS:

The yield rate of mSVF obtained from MCAM was significantly higher than that with the conventional method, although use of the device resulted in a slight decrease in cell viability. After culture, mASCs exhibited a remarkable clonogenic potential and significantly higher cell proliferation potential than cASCs. The mASCs also displayed a distinct pattern of ASC cell surface markers, increased expression of genes related to CD34, high pluripotency, and a high trilineage differentiation ability.

CONCLUSION:

The specialized device enhanced the yield of SVF and produced cells with high proliferation rates and characteristics that include expression of stem cell markers.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stem Cells / Cell Differentiation / Adipose Tissue / Cell Proliferation Limits: Humans Language: En Journal: Tissue Cell Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stem Cells / Cell Differentiation / Adipose Tissue / Cell Proliferation Limits: Humans Language: En Journal: Tissue Cell Year: 2024 Document type: Article Country of publication: