Injectable Hydrogels with In Situ Double Network Formation Enhance Retention of Transplanted Stem Cells

被引:275
作者
Cai, Lei [1 ]
Dewi, Ruby E. [1 ]
Heilshorn, Sarah C. [1 ,2 ]
机构
[1] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
EXTRACELLULAR-MATRIX; PHYSICAL HYDROGELS; PROTEIN HYDROGELS; SURVIVAL; DELIVERY; CARDIOMYOCYTES; VIABILITY; DIFFUSION; SCAFFOLD; THERAPY;
D O I
10.1002/adfm.201403631
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Stem cell transplantation via direct injection is a minimally invasive strategy being explored for treatment of a variety of injuries and diseases. Injectable hydrogels with shear moduli <50 Pa can mechanically protect cells during the injection process; however, these weak gels typically biodegrade within 1-2 weeks, which may be too fast for many therapeutic applications. To address this limitation, an injectable hydrogel is designed that undergoes two different physical crosslinking mechanisms. The first crosslinking step occurs ex vivo through peptide-based molecular recognition to encapsulate cells within a weak gel that provides mechanical protection from injection forces. The second crosslinking step occurs in situ to form a reinforcing network that significantly retards material biodegradation and prolongs cell retention time. Human adipose-derived stem cells are transplanted into the subcutaneous space of a murine model using hand-injection through a 28-gauge syringe needle. Cells delivered within the double-network hydrogel are significantly protected from mechanical damage and have significantly enhanced in vivo cell retention rates compared to delivery within saline and single network hydrogels. These results demonstrate that in situ formation of a reinforcing network within an already existing hydrogel can greatly improve transplanted cell retention, thereby enhancing potential regenerative medicine therapies.
引用
收藏
页码:1344 / 1351
页数:8
相关论文
共 62 条
[1]
Aguado BA, 2012, TISSUE ENG PT A, V18, P806, DOI [10.1089/ten.tea.2011.0391, 10.1089/ten.TEA.2011.0391]
[2]
Optimization of Parameters for a More Efficient Use of Adipose-Derived Stem Cells in Regenerative Medicine Therapies [J].
Aguena, Meire ;
Fanganiello, Roberto Dalto ;
Lorico Tissiani, Luiz Alexandre ;
Andre Ishiy, Felipe Augusto ;
Atique, Rodrigo ;
Alonso, Nivaldo ;
Passos-Bueno, Maria Rita .
STEM CELLS INTERNATIONAL, 2012, 2012
[3]
Understanding drug release from poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide) gels [J].
Anderson, BC ;
Pandit, NK ;
Mallapragada, SK .
JOURNAL OF CONTROLLED RELEASE, 2001, 70 (1-2) :157-167
[4]
Injectable Multidomain Peptide Nanofiber Hydrogel as a Delivery Agent for Stem Cell Secretome [J].
Bakota, Erica L. ;
Wang, Yin ;
Danesh, Farhad R. ;
Hartgerink, Jeffrey D. .
BIOMACROMOLECULES, 2011, 12 (05) :1651-1657
[5]
Cell transplantation therapy for stroke [J].
Bliss, Tonya ;
Guzman, Raphael ;
Daadi, Marcel ;
Steinberg, Gary K. .
STROKE, 2007, 38 (02) :817-826
[6]
Myocardial homing of nonmobilized peripheral-blood CD34+ cells after intracoronary injection [J].
Blocklet, Didier ;
Toungouz, Michel ;
Berkenboom, Guy ;
Lambermont, Micheline ;
Unger, Philippe ;
Preumont, Nicolas ;
Stoupel, Eric ;
Egrise, Dominique ;
Degaute, Jean-Paul ;
Goldman, Michel ;
Goldman, Serge .
STEM CELLS, 2006, 24 (02) :333-336
[7]
Injectable fibrin scaffold improves cell transplant survival, reduces infarct expansion, and induces neovasculature formation in ischemic myocardium [J].
Christman, KL ;
Vardanian, AJ ;
Fang, QZ ;
Sievers, RE ;
Fok, HH ;
Lee, RJ .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2004, 44 (03) :654-660
[8]
In vitro analysis of PNIPAAm-PEG, a novel, injectable scaffold for spinal cord repair [J].
Comolli, Noelle ;
Neuhuber, Birgit ;
Fischer, Itzhak ;
Lowman, Anthony .
ACTA BIOMATERIALIA, 2009, 5 (04) :1046-1055
[9]
Design of biomaterials to enhance stem cell survival when transplanted into the damaged central nervous system [J].
Cooke, M. J. ;
Vulic, K. ;
Shoichet, M. S. .
SOFT MATTER, 2010, 6 (20) :4988-4998
[10]
In vivo bioluminescence for tracking cell fate and function [J].
de Almeida, Patricia E. ;
van Rappard, Juliaan R. M. ;
Wu, Joseph C. .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2011, 301 (03) :H663-H671