Intracellular Release of 17-β Estradiol from Cationic Polyamidoamine Dendrimer Surface-Modified Poly (Lactic-co-Glycolic Acid) Microparticles Improves Osteogenic Differentiation of Human Mesenchymal Stromal Cells

被引:1
作者
Hong, Liu [1 ]
Krishnamachari, Yogita [2 ]
Seabold, Denise [1 ]
Joshi, Vijaya [2 ]
Schneider, Galen [1 ]
Salem, Aliasger K. [2 ]
机构
[1] Univ Iowa, Coll Dent, Dow Inst Dent Res, Iowa City, IA 52242 USA
[2] Univ Iowa, Coll Pharm, Div Pharmaceut, Iowa City, IA 52242 USA
基金
美国国家卫生研究院;
关键词
HUMAN BONE-MARROW; STEM-CELLS; IN-VITRO; MESSENGER-RNA; PROTEINS;
D O I
10.1089/ten.tec.2010.0388
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Human bone marrow mesenchymal stromal cells (MSCs) are considered a potential cell source for MSC-based bone regeneration, but improvements in the proliferation and differentiation capacity of MSCs are necessary for practical applications. Estrogen effectively improves MSC capabilities and has strong potential as a regulator of MSCs. The aim of this study was to develop a delivery system that provides intracellular release of estrogen and test its ability to improve osteogenic differentiation of MSCs. Biodegradable poly (lactic-co-glycolic acid) (PLGA) microparticles were developed that entrap 17-beta estradiol (E2) and provide intracellular release of E2. The results show that we can prepare PLGA particles with efficient loading of E2 and maintain release of E2 up to 7 days. Surface modifying E2-loaded PLGA particles with cationic polyamidoamine dendrimers enabled increased uptake by human MSCs. Human MSC uptake of the E2-loaded PLGA particles significantly upregulates osteogenic differentiation markers of alkaline phosphatase and osteocalcin. In conclusion, cationic-modified PLGA particles can serve as a tool for intracellular delivery of estrogen to effectively execute estrogen regulation of MSCs. This approach has the potential to improve the osteogenic capabilities of MSCs and to develop appropriate environments of implantation for MSC-based bone tissue engineering.
引用
收藏
页码:319 / 325
页数:7
相关论文
共 34 条
[21]  
Oreffo ROC, 1999, J CELL BIOCHEM, V75, P382, DOI 10.1002/(SICI)1097-4644(19991201)75:3<382::AID-JCB4>3.0.CO
[22]  
2-N
[23]   Multilineage potential of adult human mesenchymal stem cells [J].
Pittenger, MF ;
Mackay, AM ;
Beck, SC ;
Jaiswal, RK ;
Douglas, R ;
Mosca, JD ;
Moorman, MA ;
Simonetti, DW ;
Craig, S ;
Marshak, DR .
SCIENCE, 1999, 284 (5411) :143-147
[24]   The genetics of induced pluripotency [J].
Ralston, Amy ;
Rossant, Janet .
REPRODUCTION, 2010, 139 (01) :35-44
[25]   Effect of oestradiol on cytokine production in immortalized human marrow stromal cell lines [J].
Ramalho, AC ;
Jullienne, A ;
Couttet, P ;
Graulet, AM ;
Morieux, C ;
de Vernejoul, MC ;
Cohen-Solal, ME .
CYTOKINE, 2001, 16 (04) :126-130
[26]  
Rodríguez JP, 1999, J CELL BIOCHEM, V75, P414, DOI 10.1002/(SICI)1097-4644(19991201)75:3<414::AID-JCB7>3.3.CO
[27]  
2-3
[28]   Aging is associated with decreased maximal life span and accelerated senescence of bone marrow stromal cells [J].
Stenderup, K ;
Justesen, J ;
Clausen, C ;
Kassem, M .
BONE, 2003, 33 (06) :919-926
[29]   Phenotypic changes of adult porcine mesenchymal stem cells induced by prolonged passaging in culture [J].
Vacanti, V ;
Kong, E ;
Suzuki, G ;
Sato, K ;
Canty, JM ;
Lee, TC .
JOURNAL OF CELLULAR PHYSIOLOGY, 2005, 205 (02) :194-201
[30]   Principles of encapsulating hydrophobic drugs in PLA/PLGA microparticles [J].
Wischke, Christian ;
Schwendeman, Steven P. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2008, 364 (02) :298-327