Genetic and cellular therapies for cerebral infarction

被引:6
作者
Szentirmai, O
Carter, BS
机构
[1] Massachusetts Gen Hosp, Neurosurg Serv, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Lab Genet & Cellular Engn, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
关键词
cellular therapy; cerebral infarct; gene therapy; neuroregeneration; stem cells; stroke;
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
NEUROSURGEONS, WORKING AS surgical scientists, can have a prominent role in developing and implementing genetic and cellular therapies for cerebral ischemia. The rapid emergence of both genetic and cellular therapies for neural regeneration warrants a careful analysis before implementation of human studies to understand the pitfalls and promises of this strategy. In this article, we review the topic of genetic and cellular therapy for stroke to provide a foundation for practicing neurosurgeons and clinical scientists who may become involved in this type of work. In Part 1, we review preclinical approaches with gene transfer, such as 1) improved energy delivery, 2) reduction of intracellular calcium availability, 3) abrogation of effects of reactive oxygen species, 4) reduction of proinflammatory cytokine signaling, 5) inhibition of apoptosis mediators, and 6) restorative gene therapy, that are paving the way to develop new strategies to treat cerebral infarction. In Part 2, we discuss the results of studies that address the possibility of using cellular therapies for stroke in animal models and in human trials by reviewing 1) the basics of stem cell biology, 2) exogenous and 3) and endogenous cell sources for therapy, and 4) clinical considerations in cell therapy applications. These emerging technologies based on the advancements made in recent years in the fields of genetics, therapeutic cloning, neuroscience, stem cell biology, and gene therapy provide significant potential for new therapies for stroke.
引用
收藏
页码:283 / 296
页数:14
相关论文
共 119 条
[11]   Transplantation of cryopreserved human embryonal carcinoma-derived neurons (NT2N cells) promotes functional recovery in ischemic rats [J].
Borlongan, CV ;
Tajima, Y ;
Trojanowski, JQ ;
Lee, VMY ;
Sanberg, PR .
EXPERIMENTAL NEUROLOGY, 1998, 149 (02) :310-321
[12]   From marrow to brain: Expression of neuronal phenotypes in adult mice [J].
Brazelton, TR ;
Rossi, FMV ;
Keshet, GI ;
Blau, HM .
SCIENCE, 2000, 290 (5497) :1775-1779
[13]   Xenotransplantation for CNS repair: immunological barriers and strategies to overcome them [J].
Brevig, T ;
Holgersson, J ;
Widner, H .
TRENDS IN NEUROSCIENCES, 2000, 23 (08) :337-344
[14]   Cloning and characterization of rat caspase-9: Implications for a role in mediating caspase-3 activation and hippocampal cell death after transient cerebral ischemia [J].
Cao, GD ;
Luo, YM ;
Nagayama, T ;
Pei, W ;
Stetler, RA ;
Graham, SH ;
Chen, J .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2002, 22 (05) :534-546
[15]   Failure of bone marrow cells to transdifferentiate into neural cells in vivo [J].
Castro, RF ;
Jackson, KA ;
Goodell, MA ;
Robertson, CS ;
Liu, H ;
Shine, HD .
SCIENCE, 2002, 297 (5585) :1299-1299
[16]   Intracerebral transplantation of bone marrow with BDNF after MCAo in rat [J].
Chen, JL ;
Li, Y ;
Chopp, M .
NEUROPHARMACOLOGY, 2000, 39 (05) :711-716
[17]   Intravenous administration of human umbilical cord blood reduces behavioral deficits after stroke in rats [J].
Chen, JL ;
Sanberg, PR ;
Li, Y ;
Wang, L ;
Lu, M ;
Willing, AE ;
Sanchez-Ramos, J ;
Chopp, M .
STROKE, 2001, 32 (11) :2682-2688
[18]   Therapeutic benefit of intravenous administration of bone marrow stromal cells after cerebral ischemia in rats [J].
Chen, JL ;
Li, Y ;
Wang, L ;
Zhang, ZG ;
Lu, DY ;
Lu, M ;
Chopp, M .
STROKE, 2001, 32 (04) :1005-1011
[19]  
Choi J, 2001, GLIA, V33, P45, DOI 10.1002/1098-1136(20010101)33:1<45::AID-GLIA1005>3.0.CO
[20]  
2-A