Perlecan Domain V Therapy for Stroke: A Beacon of Hope?

被引:16
作者
Bix, Gregory J. [1 ]
机构
[1] Univ Kentucky, Dept Anat & Neurobiol, Sanders Brown Ctr Aging, Lexington, KY 40536 USA
关键词
Stroke; perlecan; neurogenesis; angiogenesis; neuroprotection; astrogliosis; FOCAL CEREBRAL-ISCHEMIA; OSTEOPONTIN; NEUROPROTECTION; ANGIOGENESIS; ENDOREPELLIN; ENDOTHELIN-1; RECEPTORS; GROWTH; INJURY; REPAIR;
D O I
10.1021/cn300197y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The sad reality is that in the year 2012, people are still dying or suffering from the extreme morbidity of ischemic stroke. This tragedy is only compounded by the graveyard full of once promising new therapies. While it is indeed true that the overall mortality from stroke has declined in the United States, perhaps due to increased awareness of stroke symptoms by both the lay public and physicians, it is clear that better therapies are needed. In this regard, progress has been tremendously slowed by the simple fact that experimental models of stroke and the animals that they typically employ, rats and mice, do not adequately represent human stroke. Furthermore, the neuroprotective therapeutic approach, in which potential treatments are administered with the hope of preventing the spread of dying neurons that accompanies a stroke, typically fail for a number of reasons such as there is simply more brain matter to protect in a human than there is in a rodent! For this reason, there has been somewhat of a shift in stroke research away from neuroprotection and toward a neurorepair approach. This too may be problematic in that agents that might foster brain repair could be acutely deleterious or neurotoxic and vice versa, making the timing of treatment administration after stroke critical. Therefore, in our efforts to discover a new stroke therapy, we decided to focus on identifying brain repair elements that were (1) endogenously and actively generated in response to stroke in both human and experimental animal brains, (2) present acutely and chronically after ischemic stroke, suggesting that they could have a role in acute neuroprotection and chronic neurorepair, and (3) able to be administered peripherally and reach the site of stroke brain injury. In this review, I will discuss the evidence that suggests that perlecan domain V may be just that substance, a potential beacon of hope for stroke patients.
引用
收藏
页码:370 / 374
页数:5
相关论文
共 33 条
[1]   Perlecan Domain V Modulates Astrogliosis In Vitro and After Focal Cerebral Ischemia Through Multiple Receptors and Increased Nerve Growth Factor Release [J].
Al-Ahmad, Abraham J. ;
Lee, Boyeon ;
Saini, Maxim ;
Bix, Gregory J. .
GLIA, 2011, 59 (12) :1822-1840
[2]   Recanalization therapy for acute ischemic stroke, part 2: mechanical intra-arterial technologies [J].
Ansari, Saeed ;
Rahman, Maryam ;
McConnell, Douglas J. ;
Waters, Michael F. ;
Hoh, Brian L. ;
Mocco, J. .
NEUROSURGICAL REVIEW, 2011, 34 (01) :11-19
[3]   Signaling, delivery and age as emerging issues in the benefit/risk ratio outcome of tPA For treatment of CNS ischemic disorders [J].
Armstead, William M. ;
Ganguly, Kumkum ;
Kiessling, J. W. ;
Riley, John ;
Chen, Xiao-Han ;
Smith, Douglas H. ;
Stein, Sherman C. ;
Higazi, Abd A. R. ;
Cines, Douglas B. ;
Bdeir, Khalil ;
Zaitsev, Sergei ;
Muzykantov, Vladimir R. .
JOURNAL OF NEUROCHEMISTRY, 2010, 113 (02) :303-312
[4]   Novel interactions of perlecan: Unraveling perlecan's role in angiogenesis [J].
Bix, Gregory ;
Iozzo, Renato V. .
MICROSCOPY RESEARCH AND TECHNIQUE, 2008, 71 (05) :339-348
[5]   Endorepellin in vivo: Targeting the tumor vasculature and retarding cancer growth and metabolism [J].
Bix, Gregory ;
Castello, Remedios ;
Burrows, Michelle ;
Zoeller, Jason J. ;
Weech, Michelle ;
Iozzo, Rex A. ;
Cardi, Christopher ;
Thakur, Mathew L. ;
Barker, Christopher A. ;
Camphausen, Kevin ;
Iozzo, Renato V. .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2006, 98 (22) :1634-1646
[6]   Osteopontin Reduced Hypoxia-Ischemia Neonatal Brain Injury by Suppression of Apoptosis in a Rat Pup Model [J].
Chen, Wanqiu ;
Ma, Qingyi ;
Suzuki, Hidenori ;
Hartman, Richard ;
Tang, Jiping ;
Zhang, John H. .
STROKE, 2011, 42 (03) :764-769
[7]   Perlecan Domain V Induces VEGf Secretion in Brain Endothelial Cells through Integrin α5β1 and ERK-Dependent Signaling Pathways [J].
Clarke, Douglas N. ;
Al Ahmad, Abraham ;
Lee, Boyeon ;
Parham, Christi ;
Auckland, Lisa ;
Fertala, Andrezj ;
Kahle, Michael ;
Shaw, Courtney S. ;
Roberts, Jill ;
Bix, Gregory J. .
PLOS ONE, 2012, 7 (09)
[8]   Nasal administration of osteopontin peptide mimetics confers neuroprotection in stroke [J].
Doyle, Kristian P. ;
Yang, Tao ;
Lessov, Nikola S. ;
Ciesielski, Thomas M. ;
Stevens, Susan L. ;
Simon, Roger P. ;
King, Jeffrey S. ;
Stenzel-Poore, Mary P. .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2008, 28 (06) :1235-1248
[9]   Focal cerebral ischemia induces active proteases that degrade microvascular matrix [J].
Fukuda, S ;
Fini, CA ;
Mabuchi, T ;
Koziol, JA ;
Eggleston, LL ;
del Zoppo, GJ .
STROKE, 2004, 35 (04) :998-1004
[10]   BMP-1/tolloid-like metalloproteases process endorepellin, the angiostatic C-terminal fragment of perlecan [J].
Gonzalez, EM ;
Reed, CC ;
Bix, G ;
Fu, J ;
Zhang, Y ;
Gopalakrishnan, B ;
Greenspan, DS ;
Iozzo, RV .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (08) :7080-7087