Biological and clinical availability of adipose- derived stem cells for pelvic dead space repair

Hidekazu Takahashi, Naotsugu Haraguchi, Shimpei Nishikawa, Susumu Miyazaki, Yozou Suzuki, Tsunekazu Mizushima, Junichi Nishimura, Ichirou Takemasa, Hirofumi Yamamoto, Koshi Mimori, Hideshi Ishii, Yuichiro Doki, Masaki Mori

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

Adipose-derived stem cells (ADSCs) are a very attractive cell source for regenerative and reconstructive medicine. Although ADSCs have already been used in cardiovascular disease and cosmetic surgery, they have not yet been used in gastroenterological surgery. In this study, we clarified the utility of the combined application of ADSCs and resected intraperitoneal fatty tissues as a sealant for the pelvic dead space that sometimes causes severe and fatal complications in colorectal and gynecological surgeries. In pelvic dead space model mice, mouse ADSCs efficiently maintained transplanted intraperitoneal fatty tissues without any incidence of adhesion to surrounding organs. In vivo and in vitro analyses revealed that transplanted ADSCs differentiated into endothelial cells by expressing the angiogenic factors vascular endothelial growth factor and hepatocyte growth factor. Mouse and human ADSCs contained a CD45-CD34+ subset possessing high colony formation and sphere formation abilities. In addition, the CD45-CD34+ subset consisted of two characteristic subsets: the CD34+CD90+ angiogenic subset and the CD34+CD90- adipogenic subset. Grafts of human ADSCs with fat transplanted into mice were efficiently maintained for more than 12 months without volume reductions. A comparative study of graft maintenance efficacy between cultured human ADSCs and freshly isolated ADSCs indicated that the cultivation of ADSCs decreased their graft maintenance ability. These findings suggested that the angiogenic and adipogenic subsets act in coordination with each other and are essential for efficient graft maintenance.

Original languageEnglish
Pages (from-to)803-810
Number of pages8
JournalStem Cells Translational Medicine
Volume1
Issue number11
DOIs
Publication statusPublished - 2012

All Science Journal Classification (ASJC) codes

  • Developmental Biology
  • Cell Biology

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