首页> 外文期刊>The European Journal of Neuroscience >Matrix metalloproteinase (MMP)-12 expression has a negative impact on sensorimotor function following intracerebral haemorrhage in mice.
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Matrix metalloproteinase (MMP)-12 expression has a negative impact on sensorimotor function following intracerebral haemorrhage in mice.

机译:小鼠脑出血后基质金属蛋白酶(MMP)-12表达对感觉运动功能有负面影响。

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We investigated the role of matrix metalloproteinases (MMPs) in a mouse model of intracerebral haemorrhage (ICH). Transcripts encoding nine of the 23 known mammalian MMPs were measured. MMP-12 levels were the most elevated. To evaluate the role of MMP-12 in ICH, haemorrhages were induced in wild-type (WT) and MMP-12 null mice. The results show that MMP-12 null mice exhibited significant functional recovery of forelimb reaching and reduced dependence on the ipsilateral forelimb compared to WT mice. There was also a trend for improved sensory function in the tape removal test. With respect to single pellet skilled reaching, MMP-12 null mice recovered to a level that was not significantly different from sham at 14 and 28 days post-ICH. In contrast, WT animals demonstrated a persistent impairment relative to sham controls throughout the survival period (P < 0.05). The cylinder task revealed a lesion-induced reliance on the ipsilateral forelimb that was apparent at day 7 in both MMP-12 null and WT mice (P <0.05), but only persisted in WT mice at 14 days post-ICH (P < 0.05). Differences in functional outcome could not be explained by tissue sparing. However, Iba1 immunostaining indicated that more cells bearing macrophage morphology were recruited to the lesion area in WT mice. This is the first study to profile the expression patterns of a number of the known MMPs following ICH in mice. The data indicate that MMP-12 expression following haemorrhagic stroke is deleterious and contributes to the development of secondary injury in this disease.
机译:我们调查了脑出血(ICH)小鼠模型中基质金属蛋白酶(MMP)的作用。测量了编码23种已知哺乳动物MMP中9种的转录本。 MMP-12水平最高。为了评估MMP-12在ICH中的作用,在野生型(WT)和MMP-12 null小鼠中诱发了出血。结果表明,与WT小鼠相比,MMP-12缺失小鼠表现出前肢到达的显着功能恢复,并且对同侧前肢的依赖性降低。带剥离测试中还存在改善感官功能的趋势。关于单药丸熟练到达者,MMP-12无效小鼠恢复至与ICH后14和28天假手术无明显差异的水平。相反,相对于假对照,野生动物在整个生存期内均表现出持续性损伤(P <0.05)。圆柱体任务显示病变诱导的对同侧前肢的依赖在第7天在MMP-12 null和WT小鼠中均很明显(P <0.05),但仅在ICH后14天才在WT小鼠中持续存在(P <0.05 )。功能上的差异不能通过组织保留来解释。但是,Iba1免疫染色表明,WT小鼠的病变区域募集了更多具有巨噬细胞形态的细胞。这是第一个研究小鼠ICH后多种已知MMPs表达模式的研究。数据表明出血性中风后MMP-12表达有害,并导致该疾病继发性损伤的发展。

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