Adult cell therapy for brain neuronal damages and the role of tissue engineering

被引:132
作者
Delcroix, Gaetan J. -R. [1 ,2 ]
Schiller, Paul C. [3 ,4 ,5 ,6 ,7 ,8 ]
Benoit, Jean-Pierre [1 ,2 ]
Montero-Menei, Claudia N. [1 ,2 ]
机构
[1] INSERM, U646, 10 Rue Andre Boquel, F-49100 Angers, France
[2] Univ Angers, UMR S646, F-49100 Angers, France
[3] Vet Affairs Med Ctr, Ctr Geriatr Res Educ & Clin, Miami, FL 33125 USA
[4] Vet Affairs Med Ctr, Res Serv, Miami, FL 33125 USA
[5] Univ Miami, Miller Sch Med, Geriatr Inst, Miami, FL 33136 USA
[6] Univ Miami, Miller Sch Med, Interdisciplinary Stem Cell Inst, Miami, FL 33136 USA
[7] Univ Miami, Miller Sch Med, Dept Med, Miami, FL 33136 USA
[8] Univ Miami, Miller Sch Med, Dept Biochem & Mol Biol, Miami, FL 33136 USA
关键词
Brain disorders; Mesenchymal stromal cells; Adult cells; Scaffolds; Biomimetic surface; Pharmacologically active microcarriers; MESENCHYMAL STEM-CELLS; MARROW STROMAL CELLS; PHARMACOLOGICALLY ACTIVE MICROCARRIERS; ADRENAL CHROMAFFIN CELLS; TRANSPLANTED BONE-MARROW; PARKINSONS-DISEASE; FUNCTIONAL RECOVERY; HUNTINGTONS-DISEASE; NEURITE OUTGROWTH; INTRACEREBRAL TRANSPLANTATION;
D O I
10.1016/j.biomaterials.2009.11.084
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
No long term effective treatments are currently available for brain neurological disorders such as stroke/cerebral ischemia, traumatic brain injury and neurodegenerative disorders. Cell therapy is a promising strategy, although alternatives to embryonic/foetal cells are required to overcome ethical, tissue availability and graft rejection concerns. Adult cells may be easily isolated from the patient body, therefore permitting autologous grafts to be performed. Here, we describe the use of adult neural stem cells, adrenal chromaffin cells and retinal pigment epithelium cells for brain therapy, with a special emphasis on mesenchymal stromal cells. However, major problems like cell survival, control of differentiation and engraftment remain and may be overcome using a tissue engineering strategy, which provides a 3D support to grafted cells improving their survival. New developments, such as the biomimetic approach which combines the use of scaffolds with extracellular matrix molecules, may improve the control of cell proliferation, survival, migration, differentiation and engraftment in vivo. Therefore, we later discuss scaffold properties required for brain cell therapy as well as new tissue engineering advances that may be implemented in combination with adult cells for brain therapy. Finally, we describe an approach developed in our laboratory to repair/protect lesioned tissues: the pharmacologically active microcarriers. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2105 / 2120
页数:16
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