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Bioactive calcium silicate extracts regulate the morphology and stemness of human embryonic stem cells at the initial stage
Zhang F; Lv DY(吕东媛); Li HY; Luo CH; Chang J; Long M(龙勉); Long, M (reprint author), Chinese Acad Sci, Inst Mech, Ctr Biomech & Bioengn, Beijing 100190, Peoples R China.; Long, M (reprint author), Chinese Acad Sci, Inst Mech, Natl Micrograv Lab, Key Lab Micrograv, Beijing 100190, Peoples R China.; Long, M (reprint author), Chinese Acad Sci, Inst Mech, Beijing Key Lab Engn Construct & Mechanobiol, Beijing 100190, Peoples R China.; Chang, J (reprint author), Chinese Acad Sci, Shanghai Inst Ceram, Biomat & Tissue Engn Res Ctr, Shanghai 200050, Peoples R China.
Source PublicationRSC ADVANCES
2016
Volume6Issue:106Pages:104666-104674
ISSN2046-2069
AbstractEmbryonic stem cells (ESCs) are undifferentiated cells that have the capacity to self-renew and differentiate into a variety of cells and provide cell sources for regenerative medicine or biological specimens for cytotoxicity tests. Calcium silicate (CS), a bioactive silicate ceramic, can stimulate the osteogenic differentiation of various types of stem cells, but its role in regulating the biological phenotypes of ESCs remains unclear. Here, the impact of CS on human ESCs was investigated using CS-supplemented medium. The cytotoxicity of CS to hESCs and its effects on apoptosis, growth, proliferation, and differentiation were quantified systematically. Morphological analysis of hESC colonies indicated that the bioactive ions released from CS have little cytotoxicity to hESCs at two CS concentrations. Immunofluorescence and flow cytometry analyses showed that apoptosis was time-independent at early or late stages of hESC growth. In contrast, CS ion extracts regulated hESC differentiation in a time-dependent manner: ESC stemness was preserved by enhancing Oct-4, Sox-2, and Nanog gene expression at day 3, while the cells tended to differentiate at day 6. Combined tests on gene and protein levels further indicated that hESCs tended to differentiate into mesoderm in the presence of CS ion extracts, especially at low CS concentrations. These results demonstrate the effects of CS extracts on hESC stemness and differentiation at the molecular and cellular levels, suggesting that CS-based biomaterials could serve as a potential regulator for ESCs in regenerative medicine.
DOI10.1039/c6ra17785a
URL查看原文
Indexed BySCI ; EI
Language英语
WOS IDWOS:000388111900097
WOS Research AreaChemistry
WOS SubjectChemistry, Multidisciplinary
Funding OrganizationNational Natural Science Foundation of China [31110103918, 31470907, 31370963, 81190132] ; National Key Basic Research Foundation of China [2011CB710904] ; Strategic Priority Research Program [XDA01030604] ; National High Technology Research and Development Program of China [2011AA020109]
DepartmentNML分子-细胞生物力学与空间生命科学
Classification二类
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Cited Times:2[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://dspace.imech.ac.cn/handle/311007/59950
Collection微重力重点实验室
Corresponding AuthorLong, M (reprint author), Chinese Acad Sci, Inst Mech, Ctr Biomech & Bioengn, Beijing 100190, Peoples R China.; Long, M (reprint author), Chinese Acad Sci, Inst Mech, Natl Micrograv Lab, Key Lab Micrograv, Beijing 100190, Peoples R China.; Long, M (reprint author), Chinese Acad Sci, Inst Mech, Beijing Key Lab Engn Construct & Mechanobiol, Beijing 100190, Peoples R China.; Chang, J (reprint author), Chinese Acad Sci, Shanghai Inst Ceram, Biomat & Tissue Engn Res Ctr, Shanghai 200050, Peoples R China.
Recommended Citation
GB/T 7714
Zhang F,Lv DY,Li HY,et al. Bioactive calcium silicate extracts regulate the morphology and stemness of human embryonic stem cells at the initial stage[J]. RSC ADVANCES,2016,6,106,:104666-104674.
APA Zhang F.,吕东媛.,Li HY.,Luo CH.,Chang J.,...&Chang, J .(2016).Bioactive calcium silicate extracts regulate the morphology and stemness of human embryonic stem cells at the initial stage.RSC ADVANCES,6(106),104666-104674.
MLA Zhang F,et al."Bioactive calcium silicate extracts regulate the morphology and stemness of human embryonic stem cells at the initial stage".RSC ADVANCES 6.106(2016):104666-104674.
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