TATVHL peptide-grafted alginate/poly(γ-glutamic acid) scaffolds with inverted colloidal crystal topology for neuronal differentiation of iPS cells

Biomaterials

Volumn 33, Issue 35, 2012, Pages 8955-8966

  Kuo, Yung Chih ^a   Chung, Chiu Yen ^a  

^a NATIONAL CHUNG CHENG UNIVERSITY   (Taiwan)

Author keywords

Alginate; Induced pluripotent stem cell; Inverted colloidal crystal scaffold; Neuron; Poly( glutamic acid); TATVHL peptide

Indexed keywords

ATOMIC RATIO; COLLOIDAL CRYSTALS; FREEFORMS; GLUTAMIC ACID; IMMUNOCHEMICAL STAINING; INTERCONNECTED PORES; NERVE TISSUE; NEURONAL DEVELOPMENT; NEURONAL DIFFERENTIATION; PLURIPOTENT; PLURIPOTENT STEM CELLS;

ADHESION; ALGINATE; AMINO ACIDS; COLLOIDS; CYTOLOGY; NEURONS; PEPTIDES; STEM CELLS; TISSUE; TOPOLOGY;

SCAFFOLDS (BIOLOGY);

ALGINIC ACID; BETA TUBULIN; INVERTED COLLOIDAL CRYSTAL SCAFFOLD; MICROSPHERE; NITROGEN; PEPTIDE; POLY(GAMMA GLUTAMIC ACID); POLYGLUTAMIC ACID; PROTEIN TRANSACTIVATOR OF TRANSCRIPTION VON HIPPEL LINDAU; TISSUE SCAFFOLD; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CELL ADHESION; CELL LINEAGE; CELL SELECTION; CELL STIMULATION; CELL VIABILITY; CONTROLLED STUDY; FLOW CYTOMETRY; HYDROGEL; IMMUNOHISTOCHEMISTRY; MOUSE; NERVE CELL; NERVE CELL DIFFERENTIATION; NERVOUS TISSUE; NEURAL STEM CELL; NEURAL STEM CELL TRANSPLANTATION; NONHUMAN; PLURIPOTENT STEM CELL; PRIORITY JOURNAL; TERATOMA; TISSUE MICROARRAY;

ALGINATES; ANIMALS; BIOCOMPATIBLE MATERIALS; CELL ADHESION; CELL DIFFERENTIATION; CELL LINE; CELL LINEAGE; CELL SURVIVAL; GLUCURONIC ACID; HEXURONIC ACIDS; INDUCED PLURIPOTENT STEM CELLS; MICE; NEURONS; PEPTIDES; POLYGLUTAMIC ACID; POROSITY; TISSUE SCAFFOLDS;

IPS;

EID: 84867140048     PISSN: 01429612     EISSN: 18785905     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2012.08.073     Document Type: Article

References (39)

1. Takahashi K., Yamanaka S. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors. Cell 2006, 126:663-676.
2. Aoi T., Yae K., Nakagawa M., Ichisaka T., Okita K., Takahashi K., et al. Generation of pluripotent stem cells from adult mouse liver and stomach cells. Science 2008, 321:699-702.
3. Kim J.B., Zaehres H., Wu G., Gentile L., Ko K., Sebastiano V., et al. Pluripotent stem cells induced from adult neural stem cells by reprogramming with two factors. Nature 2008, 454:646-650.
4. Liu H., Zhu F., Yong J., Zhang P., Hou P., Li H., et al. Generation of induced pluripotent stem cells from adult rhesus monkey fibroblasts. Cell Stem Cell 2008, 3:587-590.
5. Aasen T., Raya A., Barrero M.J., Garreta E., Consiglio A., Gonzalez F., et al. Efficient and rapid generation of induced pluripotent stem cells from human keratinocytes. Nat Biotechnol 2008, 26:1276-1284.
6. Sun N., Panetta N.J., Gupta D.M., Wilson K.D., Lee A., Jia F., et al. Feeder-free derivation of induced pluripotent stem cells from adult human adipose stem cells. Proc Natl Acad Sci U S A 2009, 106:15720-15725.
7. Ye J.H., Xu Y.J., Gao J., Yan S.G., Zhao J., Tu Q., et al. Critical-size calvarial bone defects healing in a mouse model with silk scaffolds and SATB2-modified iPSCs. Biomaterials 2011, 32:5065-5076.
8. Xie C., Hu J., Ma H., Zhang J., Chang L.J., Chen Y.E., et al. Three-dimensional growth of iPS cell-derived smooth muscle cells on nanofibrous scaffolds. Biomaterials 2011, 32:4369-4375.
9. Brafman D.A., Chang C.W., Fernandez A., Willert K., Varghese S., Chien S. Long-term human pluripotent stem cell self-renewal on synthetic polymer surfaces. Biomaterials 2010, 31:9135-9144.
10. Chen G.Y., Pang D.W., Hwang S.M., Tuan H.Y., Hu Y.C. A graphene-based platform for induced pluripotent stem cells culture and differentiation. Biomaterials 2012, 33:418-427.
11. Kuo Y.C., Ku I.N. Cartilage regeneration by novel polyethylene oxide/chitin/chitosan scaffolds. Biomacromolecules 2008, 9:2662-2669.
12. Lee J., Shanbhag S., Kotov N.A. Inverted colloidal crystals as three-dimensional microenvironments for cellular co-cultures. J Mater Chem 2006, 16:3558-3564.
13. Shanbhag S., Lee J., Kotov A.N. Diffusion in three-dimensionally ordered scaffolds with inverted colloidal crystal geometry. Biomaterials 2005, 26:5581-5585.
14. Lee J., Cuddihy M.J., Cater G.M., Kotov N.A. Engineering liver tissue spheroids with inverted colloidal crystal scaffolds. Biomaterials 2009, 30:4687-4694.
15. Nichols J.E., Cortiella J., Lee J., Niles J.A., Cuddihy M., Wang S., et al. In vitro analog of human bone marrow from 3D scaffolds with biomimetic inverted colloidal crystal geometry. Biomaterials 2009, 30:1071-1079.
16. Peramo A., Bahng J.H., Marcelo C.L., Kotov N., Martin D.C. In vitro integration of human skin dermis with porous cationic hydrogels. Acta Biomater 2009, 5:3337-3345.
17. Wu S., Suzuki Y., Kitada M., Kitaura M., Kataoka K., Takahashi J., et al. Migration, integration, and differentiation of hippocampus-derived neurosphere cells after transplantation into injured rat spinal cord. Neurosci Lett 2001, 312:173-176.
18. Prang P., Müller R., Eljaouhari A., Heckmann K., Kunz W., Weber T., et al. The promotion of oriented axonal regrowth in the injured spinal cord by alginate-based anisotropic capillary hydrogels. Biomaterials 2006, 27:3560-3569.
19. Akagi T., Matsusaki M., Akashi M. Pharmaceutical and medical applications of poly-gamma-glutamic acid 2010, Springer-Verlag, Berlin.
20. Peng S.F., Yang M.J., Su C.J., Chen H.L., Lee P.W., Wei M.C., et al. Effects of incorporation of poly(γ-glutamic acid) in chitosan/DNA complex nanoparticles on cellular uptake and transfection efficiency. Biomaterials 2009, 30:1797-1808.
21. Yang J.T., Kuo Y.C., Chiu K.H. Peptide-modified inverted colloidal crystal scaffolds with bone marrow stromal cells in the treatment for spinal cord injury. Colloids Surf B 2011, 84:198-205.
22. Kanno H., Nakano S., Kubo A., Mimura T., Tajima N., Sugimoto N. Neuronal differentiation of neural progenitor cells by intracellular delivery of synthetic oligopeptide derived from von Hippel-Lindau protein. Protein Pept Lett 2009, 16:1291-1296.
23. Kuo Y.C., Yu H.W. Transport of saquinavir across human brain-microvascular endothelial cells by poly(lactide-co-glycolide) nanoparticles with surface poly-(γ-glutamic acid). Int J Pharm 2011, 416:365-375.
24. Kuo Y.C., Tsai Y.T. Heparin-conjugated scaffolds with pore structure of inverted colloidal crystals for cartilage regeneration. Colloids Surf B 2011, 82:616-623.
25. Kuo Y.C., Leou S.N. Effects of composition, solvent, and salt particles on the physicochemical properties of polyglycolide/poly(lactide-co-glycolide) scaffolds. Biotechnol Prog 2006, 22:1664-1670.
26. Kuo Y.C., Chiu K.H. Inverted colloidal crystal scaffolds with laminin-derived peptides for neuronal differentiation of bone marrow stromal cells. Biomaterials 2011, 32:819-831.
27. Kuo Y.C., Lin C.Y. Effect of genipin-crosslinked chitin-chitosan scaffolds with hydroxyapatite modifications on the cultivation of bovine knee chondrocytes. Biotechnol Bioeng 2006, 95:132-144.
28. Whang K., Thomas C.H., Healy K.E. A novel method to fabricate bioabsorbable scaffolds. Polymer 1995, 36:837-842.
29. Li J.L., Pan J.L., Zhang L.G., Yu Y.T. Culture of hepatocytes on fructose-modified chitosan scaffolds. Biomaterials 2003, 24:2317-2322.
30. Santiago L.Y., Nowak R.W., Rubin J.P., Marra K.G. Peptide-surface modification of poly(caprolactone) with laminin-derived sequences for adipose-derived stem cell applications. Biomaterials 2006, 27:2962-2969.
31. Stachowiak A.N., Bershteyn A., Tzatzalos E., Irvine D.J. Bioactive hydrogels with an ordered cellular structure combine interconnected macroporosity and robust mechanical properties. Adv Mater 2005, 17:399-403.
32. Geiger H., Koehler A., Gunzer M. Stem cells, aging, niche, adhesion and Cdc42: a model for changes in cell-cell interactions and hematopoietic stem cell aging. Cell Cycle 2007, 6:884-887.
33. Calvi L.M., Adams G.B., Weibrecht K.W., Weber J.M., Olson D.P., Knight M.C., et al. Osteoblastic cells regulate the haematopoietic stem cell niche. Nature 2003, 425:841-846.
34. Djouad F., Delorme B., Maurice M., Bony C., Apparailly F., Louis-Plence P., et al. Microenvironmental changes during differentiation of mesenchymal stem cells towards chondrocytes. Arthritis Res Ther 2007, 9:R33.
35. Li X., Liu T., Song K., Yao L., Ge D., Bao C., et al. Culture of neural stem cells in calcium alginate beads. Biotechnol Prog 2006, 22:1683-1689.
36. Hsieh C.Y., Tsai S.P., Wang D.M., Chang Y.N., Hsieh H.J. Preparation of γ-PGA/chitosan composite tissue engineering matrices. Biomaterials 2005, 26:5617-5623.
37. Yamada H., Dezawa M., Shimazu S., Baba M., Sawada H., Kuroiwa Y., et al. Transfer of the Von Hippel-Lindau gene to neuronal progenitor cells in treatment for Parkinson's disease. Ann Neurol 2003, 54:352-359.
38. Kubo A., Yoshida T., Kobayashi N., Yokoyama T., Mimura T., Nishiguchi T., et al. Efficient generation of dopamine neuron-like cells fromskin-derived precursors with a synthetic peptide derived from von Hippel-Lindau protein. Stem Cells Dev 2009, 18:1523-1531.
39. Yamazaki Y., Kanno H., Maeda K., Yoshida T., Kobayashi N., Kubo A., et al. Engrafted VHL peptide-delivered bone marrow stromal cells promote spinal cord repair in rats. Neuroreport 2010, 21:287-292.