Conversion of human adipose-derived stem cells into functional and expandable endothelial-like cells for cell-based therapies

被引:12
作者
Cheng, Fuyi [1 ]
Zhang, Yujing [1 ]
Wang, Yuan [1 ]
Jiang, Qingyuan [2 ]
Zhao, Cheng Jian [1 ]
Deng, Jie [1 ]
Chen, Xiaolei [1 ]
Yao, Yunqi [1 ]
Xia, Zhemin [1 ]
Cheng, Lin [1 ]
Dai, Lei [1 ]
Shi, Gang [1 ]
Yang, Yang [1 ]
Zhang, Shuang [1 ]
Yu, Dechao [1 ]
Wei, Yuquan [1 ]
Deng, Hongxin [1 ]
机构
[1] Sichuan Univ, West China Hosp, Collaborat Innovat Ctr Biotherapy, State Key Lab Biotherapy & Canc Ctr, Ke Yuan Rd 4,1 Gao Peng St, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Prov Hosp Women & Children, Dept Obstet, Chengdu, Sichuan, Peoples R China
基金
国家重点研发计划;
关键词
Human adipose-derived stem cells (hADSCs); ETV2; EC-like cells; Angiogenesis; Regenerative medicine; TGF-BETA; HUMAN FIBROBLASTS; SKIN FIBROBLASTS; PROGENITOR CELLS; ANGIOGENESIS; VEGF; ETV2; ETS; MAINTENANCE; EFFICACY;
D O I
10.1186/s13287-018-1088-6
中图分类号
Q813 [细胞工程];
学科分类号
摘要
BackgroundIschemic vascular diseases are the major cause of death worldwide. In recent years, endothelial cell (EC)-based approaches to vascular regeneration are increasingly viable strategies for treating ischemic diseases, but their applications are challenged by the difficulties in their efficient generation and stable maintenance. Here, we show an alternative protocol that facilitates the generation of functional and expandable ETS variant 2 (ETV2)-induced endothelial-like cells (EiECs) from human adipose-derived stem cells (hADSCs), providing a potential source of cells for autologous ECs to treat ischemic vascular diseases.MethodshADSCs were obtained from fresh human adipose tissue. Passage 3 hADSCs were transduced with doxycycline (DOX)-inducible ETV2 transcription factor; purified ETV2-hADSCs were induced into endothelial-like cells using a two-stage induction culture system composed of small molecule compounds and cell factors. EiECs were evaluated for their surface markers, proliferation, gene expression, secretory capacity, and effects on vascular regeneration in vivo.ResultsWe found that short-term ETV2 expression combined with TGF- inhibition is sufficient for the generation of kinase insert domain receptor (KDR)+ cells from hADSCs within 10days. KDR+ cells showed immature endothelial characteristics, and they can gradually mature in a chemically defined induction medium at the second stage of induction. Futher studies showed that KDR+ cells deriving EC-like cells could stably self-renew and expand about 10(6)-fold in 1month, and they exhibited expected genome-wide molecular features of mature ECs. Functionally, these EC-like cells significantly promoted revascularization in a hind limb ischemic model.ConclusionsWe isolated highly purified hADSCs and effectively converted them into functional and expandable endothelial-like cells. Thus, the study may provide an alternative strategy to obtain functional EC-like cells with potential for biomedical and pharmaceutical applications.
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页数:15
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共 43 条
[1]   Fli1 Acts Downstream of Etv2 to Govern Cell Survival and Vascular Homeostasis via Positive Autoregulation [J].
Abedin, Md J. ;
Nguyen, Annie ;
Jiang, Nan ;
Perry, Cameron E. ;
Shelton, John M. ;
Watson, Dennis K. ;
Ferdous, Anwarul .
CIRCULATION RESEARCH, 2014, 114 (11) :1690-+
[2]   Chromatin dynamics during cellular reprogramming [J].
Apostolou, Effie ;
Hochedlinger, Konrad .
NATURE, 2013, 502 (7472) :462-471
[3]   A protocol for isolation and culture of human umbilical vein endothelial cells [J].
Baudin, Bruno ;
Bruneel, Arnaud ;
Bosselut, Nelly ;
Vaubourdolle, Michel .
NATURE PROTOCOLS, 2007, 2 (03) :481-485
[4]   Shear stress and VEGF enhance endothelial differentiation of human adipose-derived stem cells [J].
Colazzo, Francesca ;
Alrashed, Fahad ;
Saratchandra, Padmini ;
Carubelli, Ivan ;
Chester, Adrian H. ;
Yacoub, Magdi H. ;
Taylor, Patricia M. ;
Somers, Pamela .
GROWTH FACTORS, 2014, 32 (05) :139-149
[5]   Transcriptional Control of Endothelial Cell Development [J].
De Val, Sarah ;
Black, Brian L. .
DEVELOPMENTAL CELL, 2009, 16 (02) :180-195
[6]   Combinatorial Regulation of Endothelial Gene Expression by Ets and Forkhead Transcription Factors [J].
De Val, Sarah ;
Chi, Neil C. ;
Meadows, Stryder M. ;
Minovitsky, Simon ;
Anderson, Joshua P. ;
Harris, Ian S. ;
Ehlers, Melissa L. ;
Agarwal, Pooja ;
Visel, Axel ;
Xu, Shan-Mei ;
Pennacchio, Len A. ;
Dubchak, Inna ;
Krieg, Paul A. ;
Stainier, Didier Y. R. ;
Black, Brian L. .
CELL, 2008, 135 (06) :1053-1064
[7]   Stem cell therapy for chronic ischaemic heart disease and congestive heart failure [J].
Fisher, Sheila A. ;
Doree, Carolyn ;
Mathur, Anthony ;
Taggart, David P. ;
Martin-Rendon, Enca .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2016, (12)
[8]   Stem cell-based peripheral vascular regeneration [J].
Fujita, Yasuyuki ;
Kawamoto, Atsuhiko .
ADVANCED DRUG DELIVERY REVIEWS, 2017, 120 :25-40
[9]   Efficient Direct Reprogramming of Mature Amniotic Cells into Endothelial Cells by ETS Factors and TGFβ Suppression [J].
Ginsberg, Michael ;
James, Daylon ;
Ding, Bi-Sen ;
Nolan, Daniel ;
Geng, Fuqiang ;
Butler, Jason M. ;
Schachterle, William ;
Pulijaal, Venkat R. ;
Mathew, Susan ;
Chasen, Stephen T. ;
Xiang, Jenny ;
Rosenwaks, Zev ;
Shido, Koji ;
Elemento, Olivier ;
Rabbany, Sina Y. ;
Rafii, Shahin .
CELL, 2012, 151 (03) :559-575
[10]   Direct Conversion of Adult Skin Fibroblasts to Endothelial Cells by Defined Factors [J].
Han, Jung-Kyu ;
Chang, Sung-Hwan ;
Cho, Hyun-Ju ;
Choi, Saet-Byeol ;
Ahn, Hyo-Suk ;
Lee, Jaewon ;
Jeong, Heewon ;
Youn, Seock-Won ;
Lee, Ho-Jae ;
Kwon, Yoo-Wook ;
Cho, Hyun-Jai ;
Oh, Byung-Hee ;
Oettgen, Peter ;
Park, Young-Bae ;
Kim, Hyo-Soo .
CIRCULATION, 2014, 130 (14) :1168-1178