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Fructose 1,6‐Bisphosphate as a Protective Agent for Experimental Fat Grafting

Authors :
Tao Lv
Yunpeng Gu
Jianhai Bi
Ning Kang
Zhigang Yang
Xin Fu
Qian Wang
Li Yan
Xia Liu
Yilin Cao
Ran Xiao
Source :
Stem Cells Translational Medicine, Vol 8, Iss 6, Pp 606-616 (2019)
Publication Year :
2019
Publisher :
Oxford University Press, 2019.

Abstract

Abstract Fat grafting procedures are considered to be a promising regenerative, cell‐directed therapy; however, their survival is mainly influenced by ischemia condition. Fructose 1,6‐bisphosphate (FBP), as an intermediate in energy metabolism, has the potential to rescue cells and tissues from hypoxic‐ischemic circumstances. In the present study, human lipoaspirates were grafted subcutaneously into nude mice followed by a daily intraperitoneal injection of FBP at different doses for 7 days. Next, the grafts were harvested at different time points till 12 weeks postimplantation and were evaluated for cell viability and function, tissue revascularization and inflammatory cell infiltration using histological analysis, whole‐mount living tissue imaging, glycerol 3‐phosphate dehydrogenase activity assays, and quantitative analysis of gene expression. The results demonstrated that exogenous FBP administration could attenuate the volume and weight reduction of fat graft; meanwhile, FBP enhanced adipocyte viability and function, increased blood vessel formation, and decreased inflammation. Moreover, in vitro cell experiments showed that FBP could promote adipose‐derived stem cell viability and vascular endothelial growth factor (VEGF) mRNA expression in ischemia conditions. Our study indicates that FBP can be used as a protective agent for fat grafting and may be applied in stem cell‐based regenerative medicine. Stem Cells Translational Medicine 2019;8:606–616

Details

Language :
English
ISSN :
21576580 and 21576564
Volume :
8
Issue :
6
Database :
Directory of Open Access Journals
Journal :
Stem Cells Translational Medicine
Publication Type :
Academic Journal
Accession number :
edsdoj.9431666a9634b93b098e60f5cc20297
Document Type :
article
Full Text :
https://doi.org/10.1002/sctm.18-0212