Acute hepatocyte growth factor treatment induces long-term neuroprotection and stroke recovery via mechanisms involving neural precursor cell proliferation and differentiation

被引:61
作者
Doeppner, Thorsten R. [1 ,2 ]
Kaltwasser, Britta [2 ]
ElAli, Ayman [1 ]
Zechariah, Anil [1 ]
Hermann, Dirk M. [1 ]
Baehr, Mathias [2 ,3 ]
机构
[1] Univ Duisburg Essen, Sch Med, Dept Neurol, D-45122 Essen, Germany
[2] Univ Gottingen, Dept Neurol, Sch Med, D-3400 Gottingen, Germany
[3] DFG Res Ctr Mol Physiol Brain CMPB, Gottingen, Germany
关键词
cerebral ischemia; hepatocyte growth factor; matrix metalloproteases; neural precursor cells; neurogenesis; stroke; FOCAL CEREBRAL-ISCHEMIA; BLOOD-BRAIN-BARRIER; TRANSIENT FOREBRAIN ISCHEMIA; STEM-CELLS; SUBVENTRICULAR ZONE; NEUROTROPHIC FACTOR; RAT-BRAIN; MATRIX METALLOPROTEINASES; NEURONAL DIFFERENTIATION; ADULT BRAIN;
D O I
10.1038/jcbfm.2010.211
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hepatocyte growth factor (HGF) is an interesting candidate for acute stroke treatment as shown by continuous infusion or gene delivery protocols. However, little is known about HGF-mediated long-term effects. The present study therefore analyzed long-term effects of an acute intrastriatal HGF treatment (5 mu g) after a 45-minute stroke, with regard to brain injury and neurologic recovery. Hepatocyte growth factor induced long-term neuroprotection as assessed by infarct volume and neuronal cell death analysis for as long as 4 weeks after stroke, which was associated with sustained neurologic recovery as evidenced by corner-turn and tight-rope tests. Analyzing underlying mechanisms of HGF-induced sustained neuroprotection, enhanced cell proliferation followed by increased neuronal differentiation of neural precursor cells (NPCs) was observed in the ischemic striatum of HGF-treated mice, which persisted for up to 4 weeks. In line with this, HGF promoted neurosphere formation as well as proliferation of NPC and decreased caspase-3-dependent hypoxic injury in vitro. Preservation of blood-brain barrier integrity 24 hours after stroke was furthermore noticed in animals receiving HGF, which was associated with the inhibition of matrix metalloproteases (MMP)-2 and MMP-9 at 4 and 24 hours, respectively. We suggest that sustained recruitment of proliferating cells together with improved neurovascular remodeling provides an explanation for HGF-induced long-term neuroprotection. Journal of Cerebral Blood Flow & Metabolism(2011) 31, 1251-1262; doi:10.1038/jcbfm.2010.211; published online 1 December 2010
引用
收藏
页码:1251 / 1262
页数:12
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