Stemazole promotes survival and preserves stemness in human embryonic stem cells

被引:9
作者
Sun, Ying [1 ,2 ]
Zhang, Xiaoyan [1 ,3 ]
Li, Huajun [2 ]
Xu, Shasha [2 ]
Zhang, Xiaoyan [1 ,3 ]
Liu, Yinan [1 ]
Han, Mei [2 ]
Wen, Jinhua [1 ]
机构
[1] Peking Univ, Hlth Sci Ctr, Sch Basic Med Sci, Dept Cell Biol,Stem Cell Res Ctr, Beijing 100191, Peoples R China
[2] Beijing Normal Univ, Coll Chem, Key Lab Radiopharmaceut, Minist Educ, Beijing 100875, Peoples R China
[3] Beijing Normal Univ, Minist Educ, Key Lab Cell Proliferat & Regulat Biol, Beijing, Peoples R China
基金
北京市自然科学基金; 美国国家科学基金会;
关键词
apoptosis; human embryonic stem cell; small molecule; stemazole; REGENERATIVE MEDICINE; HUMAN BLASTOCYSTS; CHEMICAL APPROACH; SMALL MOLECULES; DIFFERENTIATION; DISEASE; LINES; DERIVATION; CULTURE; BIOLOGY;
D O I
10.1111/febs.14355
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
Human embryonic stem cells (hESCs) are extremely delicate, and survive poorly under suboptimal culture conditions, severelyrestricting long-term studies and practical applications. Thus, a protective agent that promotes stem cell survival is urgently needed. In this study, we evaluated the protective effects of stemazole in single-cell and starved hESC cultures. Colony formation was quantified by alkaline phosphatase and immunofluorescence staining, while apoptosis was assessed by flow cytometry and TUNEL assay. Expression of hESC and other stem cell markers was evaluated by western blot, RT-PCR, and qPCR. We found that stemazole enhanced clonal expansion from single cells in dose-dependent fashion and clearly decreased apoptosis from 54.1% to 25.2%. Furthermore, the drug reduced apoptosis from 43.6% to 8.4% over 15h of starvation, with 66% of stemazole-treated cells remaining viable after 2weeks of starvation. Importantly, starved cells protected with stemazole retained the same proliferation and differentiation properties as cells in normal culture. In conclusion, stemazole significantly promotes survival of stem cells in single-cell or starvation cultures without compromising stemness and pluripotency.
引用
收藏
页码:531 / 541
页数:11
相关论文
共 24 条
[1]   Clonally derived human embryonic stem cell lines maintain pluripotency and proliferative potential for prolonged periods of culture [J].
Amit, M ;
Carpenter, MK ;
Inokuma, MS ;
Chiu, CP ;
Harris, CP ;
Waknitz, MA ;
Itskovitz-Eldor, J ;
Thomson, JA .
DEVELOPMENTAL BIOLOGY, 2000, 227 (02) :271-278
[2]   Small molecules and future regenerative medicine [J].
Ding, S ;
Schultz, PG .
CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2005, 5 (04) :383-396
[3]   A role for chemistry in stem cell biology [J].
Ding, S ;
Schultz, PG .
NATURE BIOTECHNOLOGY, 2004, 22 (07) :833-840
[4]   Pharmacological potential of embryonic stem cells [J].
Gorba, T ;
Allsopp, TE .
PHARMACOLOGICAL RESEARCH, 2003, 47 (04) :269-278
[5]   Neuroprotective effects of stemazole in the MPTP-induced acute model of Parkinson's disease: Involvement of the dopamine system [J].
Guo, Zhirui ;
Xu, Shasha ;
Du, Na ;
Liu, Jia ;
Huang, Yiyun ;
Han, Mei .
NEUROSCIENCE LETTERS, 2016, 616 :152-159
[6]   Therapeutic efficacy of stemazole in a beta-amyloid injection rat model of Alzheimer's disease [J].
Han, Mei ;
Liu, Ying ;
Tan, Qi ;
Zhang, Bing ;
Wang, Wei ;
Liu, Jian ;
Zhang, Xiao-Jun ;
Wang, Yong-Yan ;
Zhang, Jin-Ming .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2011, 657 (1-3) :104-110
[7]   Mechanisms of disease: Nuclear transplantation, embryonic stem cells, and the potential for cell therapy [J].
Hochedlinger, K ;
Jaenisch, R .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (03) :275-286
[8]   Concise Review: A Chemical Approach to Control Cell Fate and Function [J].
Li, Wenlin ;
Jiang, Kai ;
Ding, Sheng .
STEM CELLS, 2012, 30 (01) :61-68
[9]   Small molecules that modulate embryonic stem cell fate and somatic cell reprogramming [J].
Li, Wenlin ;
Ding, Sheng .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2010, 31 (01) :36-45
[10]   Derivation of human embryonic stem cells in defined conditions [J].
Ludwig, TE ;
Levenstein, ME ;
Jones, JM ;
Berggren, WT ;
Mitchen, ER ;
Frane, JL ;
Crandall, LJ ;
Daigh, CA ;
Conard, KR ;
Piekarczyk, MS ;
Llanas, RA ;
Thomson, JA .
NATURE BIOTECHNOLOGY, 2006, 24 (02) :185-187