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具有脑神经元烟碱型乙酰胆碱受体(S248F)敲入突变的雌性小鼠中快肌和慢肌纤维特征的改变。

Altered fast- and slow-twitch muscle fibre characteristics in female mice with a (S248F) knock-in mutation of the brain neuronal nicotinic acetylcholine receptor.

作者信息

Cannata David J, Finkelstein David I, Gantois Ilse, Teper Yaroslav, Drago John, West Jan M

机构信息

School of Life and Environmental Sciences, Deakin University, VIC, Australia.

出版信息

J Muscle Res Cell Motil. 2009;30(1-2):73-83. doi: 10.1007/s10974-009-9177-x. Epub 2009 Apr 29.

Abstract

We generated a mouse line with a missense mutation (S248F) in the gene (CHRNA4) encoding the alpha4 subunit of neuronal nicotinic acetylcholine receptor (nAChR). Mutant mice demonstrate brief nicotine induced dystonia that resembles the clinical events seen in patients with the same mutation. Drug-induced dystonia is more pronounced in female mice, thus our aim was to determine if the S248F mutation changed the properties of fast- and slow-twitch muscle fibres from female mutant mice. Reverse transcriptase-PCR confirmed CHRNA4 gene expression in the brain but not skeletal muscles in normal and mutant mice. Ca(2+) and Sr(2+) force activation curves were obtained using skinned muscle fibres prepared from slow-twitch (soleus) and fast-twitch (EDL) muscles. Two significant results were found: (1) the (pCa(50) - pSr(50)) value from EDL fibres was smaller in mutant mice than in wild type (1.01 vs. 1.30), (2) the percentage force produced at pSr 5.5 was larger in mutants than in wild type (5.76 vs. 0.24%). Both results indicate a shift to slow-twitch characteristics in the mutant. This conclusion is supported by the identification of the myosin heavy chain (MHC) isoforms. Mutant EDL fibres expressed MHC I (usually only found in slow-twitch fibres) as well as MHC IIa. Despite the lack of spontaneous dystonic events, our findings suggest that mutant mice may be having subclinical events or the mutation results in a chronic alteration to muscle neural input.

摘要

我们构建了一种小鼠品系,其编码神经元烟碱型乙酰胆碱受体(nAChR)α4亚基的基因(CHRNA4)存在错义突变(S248F)。突变小鼠表现出短暂的尼古丁诱导的肌张力障碍,类似于具有相同突变的患者所出现的临床症状。药物诱导的肌张力障碍在雌性小鼠中更为明显,因此我们的目的是确定S248F突变是否改变了雌性突变小鼠快肌纤维和慢肌纤维的特性。逆转录聚合酶链反应(RT-PCR)证实正常小鼠和突变小鼠的大脑中CHRNA4基因表达,但骨骼肌中未表达。使用从慢肌(比目鱼肌)和快肌(趾长伸肌)制备的去皮肤肌纤维获得钙(Ca2+)和锶(Sr2+)力激活曲线。发现了两个重要结果:(1)突变小鼠趾长伸肌纤维的(pCa50 - pSr50)值小于野生型(1.01对1.30),(2)在pSr 5.5时突变体产生的力百分比大于野生型(5.76对0.24%)。这两个结果都表明突变体向慢肌特性转变。这一结论得到了肌球蛋白重链(MHC)同工型鉴定的支持。突变的趾长伸肌纤维表达MHC I(通常仅在慢肌纤维中发现)以及MHC IIa。尽管缺乏自发性肌张力障碍事件,但我们的研究结果表明突变小鼠可能存在亚临床事件,或者该突变导致肌肉神经输入的慢性改变。

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