The support of neural stem cells transplanted into stroke-induced brain cavities by PLGA particles

被引:158
作者
Bible, Ellen
Chau, David Y. S. [2 ]
Alexander, Morgan R. [3 ]
Price, Jack
Shakesheff, Kevin M. [2 ]
Modo, Michel [1 ]
机构
[1] Kings Coll London, Ctr Cellular Basis Behav, James Black Ctr, Inst Psychiat,Dept Neurosci, London SE5 9NU, England
[2] Univ Nottingham, Div Adv Drug Delivery, Ctr Biomol Sci, Sch Pharm, Nottingham NG7 2RD, England
[3] Univ Nottingham, Lab Biophys & Surface Anal, Sch Pharm, Nottingham NG7 2RD, England
基金
英国生物技术与生命科学研究理事会;
关键词
Stroke; Neural stem cells; Cell transplantation; PLGA; Scaffold particle; Tissue engineering; RETINAL PROGENITOR CELLS; ENDOTHELIAL-CELLS; IN-VITRO; TISSUE; SCAFFOLDS; RECOVERY; GRAFTS; DIFFERENTIATION; POLYMERS; SURVIVAL;
D O I
10.1016/j.biomaterials.2009.02.012
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Stroke causes extensive cellular loss that leads to a disintegration of the afflicted brain tissue. Although transplanted neural stein cells can recover some of the function lost after stroke, recovery is incomplete and restoration of lost tissue is minimal. The challenge therefore is to provide transplanted cells with matrix support in order to optimise their ability to engraft the damaged tissue. We here demonstrate that plasma polymerised allylamine (ppAAm)-treated poly(D,L-lactic acid-co-glycolic acid) (PLGA) scaffold particles can act as a structural support for neural stem cells injected directly through a needle into the lesion cavity using magnetic resonance imaging-derived co-ordinates. Upon implantation, the neuro-scaffolds integrate efficiently within host tissue forming a primitive neural tissue. These neuro-scaffolds could therefore be a more advanced method to enhance brain repair. This study provides a substantial step in the technology development required for the translation of this approach. (C) 2009 Elsevier Ltd. All rights reserved
引用
收藏
页码:2985 / 2994
页数:10
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