Co-transplantation of exosomes derived from hypoxia-preconditioned adipose mesenchymal stem cells promotes neovascularization and graft survival in fat grafting

被引:160
作者
Han, Yu-di [1 ,2 ]
Bai, Yun [1 ,3 ]
Yan, Xin-long [4 ,5 ]
Ren, Jing [1 ,2 ]
Zeng, Quan [4 ]
Li, Xiao-dong [2 ,6 ]
Pei, Xue-tao [4 ]
Han, Yan [1 ,2 ]
机构
[1] Peoples Liberat Army Gen Hosp, Dept Plast & Reconstruct Surg, Beijing 100853, Peoples R China
[2] Med Sch Chinese PLA, Beijing 100853, Peoples R China
[3] Nankai Univ, Sch Med, Tianjin 300000, Peoples R China
[4] Beijing Inst Transfus Med, Stem Cell & Regenerat Med Lab, 27 Taiping Rd, Beijing 100850, Peoples R China
[5] Beijing Univ Technol, Life Sci & Bioengn Dept, Beijing 100124, Peoples R China
[6] Bethune Int Peace Hosp, Bum & Plast Surg, Shijiazhuang 050000, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
Fat grafting; Adipose-derived stem cells; Exosomes; Angiogenesis; Microenvironment; EXTRACELLULAR VESICLES; ANGIOGENESIS;
D O I
10.1016/j.bbrc.2018.02.076
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Adipose-derived stromal cells (ADSCs)-derived exosomes (ADSC-Exos) account for the proangiogenic potential of stem cell. This study aimed to investigate the effect of ADSC-derived exosomes (ADSC-Exos) on the survival in fat grafting. Methods: A nude mouse model of subcutaneous fat grafting was adopted. Hypoxic preconditioned ADSC-Exos and ADSC-Exos were injected around the grafted tissue. The fat graft sample was weighed and examined by hematoxylin and eosin (H&E) staining and immunohistochemistry. Laser Doppler flowmetry and CD31 immunofluorescence staining were used to analyze neovascularization. Results: ADSC-Exo and hypoxic ADSC-Exo groups had a significantly higher weight of fat graft and more perilipin-positive adipocytes than the control groups from 2 to 8 weeks after grafting, and the hypoxic ADSC-Exo group had better outcomes (all P < 0.05). H&E staining showed that ADSC-Exos attenuated infiltration of inflammatory cells around the fat grafts. Laser Doppler flowmetry showed that the two ADSC-Exo groups had better blood perfusion in the graft tissue than the control groups (all P < 0.05). Immunofluorescence demonstrated that the hypoxic ADSC-Exo group had significantly more CD31-positive cells than the ADSC-Exo group. In vitro study showed that hypoxic ADSC-Exos treatment significantly increased the migration (at 12 and 24 h) and in vitro capillary network formation (at 12 h) in the human umbilical vein endothelial cells (HUVECs) as compared with the ADSC-Exo group and control group (all P < 0.05). Conclusions: Co-transplantation of ADSC-Exos can effectively promote the survival of graft, neovascularization and attenuated inflammation in the fat grafts. Hypoxia treatment can further enhance the beneficial effect of ADSC-Exos. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:305 / 312
页数:8
相关论文
共 20 条
[1]   Exosomes for repair, regeneration and rejuvenation [J].
Basu, Joydeep ;
Ludlow, John W. .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2016, 16 (04) :489-506
[2]   Using exosomes, naturally-equipped nanocarriers, for drug delivery [J].
Batrakova, Elena V. ;
Kim, Myung Soo .
JOURNAL OF CONTROLLED RELEASE, 2015, 219 :396-405
[3]   Proangiogenic Compositions of Microvesicles Derived from Human Umbilical Cord Mesenchymal Stem Cells [J].
Chen, Jianying ;
Liu, Zhenjun ;
Hong, Mian Ming ;
Zhang, Hongzhe ;
Chen, Can ;
Xiao, Mengyuan ;
Wang, Junxian ;
Yao, Feng ;
Ba, Mingchuan ;
Liu, Jinghu ;
Guo, Zi-Kuan ;
Zhong, Jixin .
PLOS ONE, 2014, 9 (12)
[4]   The Graft- to- Capacity Ratio: Volumetric Planning in Large- Volume Fat Transplantation [J].
Del Vecchio, Daniel A. ;
Del Vecchio, Sharon J. .
PLASTIC AND RECONSTRUCTIVE SURGERY, 2014, 133 (03) :561-569
[5]   Autologous Fat Transplantation: Volumetric Tools for Estimation of Volume Survival. A Systematic Review [J].
Herold, Christian ;
Ueberreiter, Klaus ;
Busche, Marc N. ;
Vogt, Peter M. .
AESTHETIC PLASTIC SURGERY, 2013, 37 (02) :380-387
[6]   Hypoxic lung cancer-secreted exosomal miR-23a increased angiogenesis and vascular permeability by targeting prolyl hydroxylase and tight junction protein ZO-1 [J].
Hsu, Y-L ;
Hung, J-Y ;
Chang, W-A ;
Lin, Y-S ;
Pan, Y-C ;
Tsai, P-H ;
Wu, C-Y ;
Kuo, P-L .
ONCOGENE, 2017, 36 (34) :4929-4942
[7]  
Hu Li., 2013, BioMed research international, V2013
[8]   Extracellular vesicles as new players in angiogenesis [J].
Kholia, Sharad ;
Ranghino, Andrea ;
Garnieri, Paolo ;
Lopatina, Tatiana ;
Deregibus, Maria Chiara ;
Rispoli, Pietro ;
Brizzi, Maria Felice ;
Camussi, Giovanni .
VASCULAR PHARMACOLOGY, 2016, 86 :64-70
[9]  
Laloze J., 2017, J TISSUE ENG REGEN M, P1
[10]   Mesenchymal stem cells promote tumor angiogenesis via the action of transforming growth factor β1 [J].
Li, Guo-Cai ;
Zhang, Hong-Wei ;
Zhao, Qing-Chun ;
Sun, Li ;
Yang, Jian-Jun ;
Hong, Liu ;
Feng, Fan ;
Cai, Lei .
ONCOLOGY LETTERS, 2016, 11 (02) :1089-1094