Extensive neurite outgrowth and active synapse formation on self-assembling peptide scaffolds

被引:980
作者
Holmes, TC
de Lacalle, S
Su, X
Liu, GS
Rich, A
Zhang, SG
机构
[1] MIT, Ctr Biomed Engn 56 341, Cambridge, MA 02139 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
[3] MIT, Dept Brain, Cambridge, MA 02139 USA
[4] MIT, Dept Cognit Sci, Ctr Learning & Memory, Cambridge, MA 02139 USA
[5] NYU, Dept Biol, New York, NY 10003 USA
[6] Calif State Univ Los Angeles, Dept Biol & Microbiol, Los Angeles, CA 90032 USA
[7] Harvard Univ, Sch Med, McLean Hosp, Belmont, MA 02478 USA
关键词
biological; materials; cell attachment; molecular material design; primary neurons; PC12; cells;
D O I
10.1073/pnas.97.12.6728
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
A new type of self-assembling peptide (sapeptide) scaffolds that serve as substrates for neurite outgrowth and synapse formation is described. These peptide-based scaffolds are amenable to molecular design by using chemical or biotechnological syntheses. They can be tailored to a variety of applications. The sapeptide scaffolds are formed through the spontaneous assembly of ionic self-complementary beta-sheet oligopeptides under physiological conditions, producing a hydrogel material. The scaffolds can support neuronal cell attachment and differentiation as well as extensive neurite outgrowth. Furthermore, they are permissive substrates for functional synapse formation between the attached neurons. That primary rat neurons form active synapses on such scaffold surfaces in situ suggests these scaffolds could be useful for tissue engineering applications. The buoyant sapeptide scaffolds with attached cells in culture can be transported readily from one environment to another. Furthermore, these peptides did not elicit a measurable immune response or tissue inflammation when introduced into animals. These biological materials created through molecular design and self assembly may be developed as a biologically compatible scaffold for tissue repair and tissue engineering.
引用
收藏
页码:6728 / 6733
页数:6
相关论文
共 40 条
[1]
POLYORNITHINE-ATTACHED NEURITE-PROMOTING FACTORS (PNPFS) - CULTURE SOURCES AND RESPONSIVE NEURONS [J].
ADLER, R ;
MANTHORPE, M ;
SKAPER, SD ;
VARON, S .
BRAIN RESEARCH, 1981, 206 (01) :129-144
[2]
Responsive gels formed by the spontaneous self-assembly of peptides into polymeric beta-sheet tapes [J].
Aggeli, A ;
Bell, M ;
Boden, N ;
Keen, JN ;
Knowles, PF ;
McLeish, TCB ;
Pitkeathly, M ;
Radford, SE .
NATURE, 1997, 386 (6622) :259-262
[3]
Conformation and ion-channeling activity of a 27-residue peptide modeled on the single-transmembrane segment of the IsK (minK) protein [J].
Aggeli, A ;
Bannister, ML ;
Bell, M ;
Boden, N ;
Findlay, JBC ;
Hunter, M ;
Knowles, PF ;
Yang, JC .
BIOCHEMISTRY, 1998, 37 (22) :8121-8131
[4]
[Anonymous], 1997, PRINCIPLES TISSUE EN
[5]
[Anonymous], 1998, FRONTIERS TISSUE ENG
[6]
BANKER G, 1997, PRIMARY DISSOCIATED, P41
[7]
BETA-STRUCTURES OF ALTERNATING POLYPEPTIDES AND THEIR POSSIBLE PREBIOTIC SIGNIFICANCE [J].
BRACK, A ;
ORGEL, LE .
NATURE, 1975, 256 (5516) :383-387
[8]
LONG-TERM EXPRESSION OF THE C-FOS PROTEIN DURING THE INVITRO DIFFERENTIATION OF CEREBELLAR GRANULE CELLS INDUCED BY POTASSIUM OR NMDA [J].
DIDIER, M ;
ROUX, P ;
PIECHACZYK, M ;
MANGEAT, P ;
DEVILLIERS, G ;
BOCKAERT, J ;
PIN, JP .
MOLECULAR BRAIN RESEARCH, 1992, 12 (1-3) :249-258
[9]
THE EXTRACELLULAR-MATRIX COORDINATELY MODULATES LIVER TRANSCRIPTION FACTORS AND HEPATOCYTE MORPHOLOGY [J].
DIPERSIO, CM ;
JACKSON, DA ;
ZARET, KS .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (09) :4405-4414
[10]
Recent advances in tissue synthesis in vivo by use of collagen-glycosaminoglycan copolymers [J].
Ellis, DL ;
Yannas, IV .
BIOMATERIALS, 1996, 17 (03) :291-299