Huang Min-Syuan, Wang Tze-Kai, Liu Yi-Wen, Li Yi-Ting, Chi Tang-Hao, Chou Chih-Wei, Hsieh Mingli
Department of Life Science, Tunghai University, Taichung 407, Taiwan, Republic of China.
Department of Life Science, Tunghai University, Taichung 407, Taiwan, Republic of China; Life Science Research Center, Tunghai University, Taichung 407, Taiwan, Republic of China.
Biochim Biophys Acta. 2014 Sep;1840(9):2829-42. doi: 10.1016/j.bbagen.2014.04.017. Epub 2014 May 1.
Carbonic anhydrase 8 (CA8) is an isozyme of α-carbonic anhydrases (CAs). Previous studies showed that CA8 can be detected in human adult brain, with more intense expression in the cerebellum. Single mutations in CA8 were reported to cause novel syndromes like ataxia, mild mental retardation or the predisposition to quadrupedal gait.
In the present study, we examine the functions of CA8 in neuronal cell lines, mouse cerebellar granule neurons and zebrafish.
We demonstrated that overexpression of CA8 in neuronal cells significantly decreased cell death under staurosporine treatment. Moreover, CA8 overexpression significantly increased cell migration and invasion ability in neuronal cells and in mouse cerebellar granule neurons, implicating that CA8 may be involved in neuron motility and oncogenesis. By using zebrafish as an animal model, motor reflection of 3dpf zebrafish embryos was significantly affected after the down-regulation of CA8 through ca8 morpholino.
We concluded that CA8 overexpression desensitizes neuronal cells to STS induced apoptotic stress and increases cell migration and invasion ability in neuronal cells. In addition, down-regulated CA8 decreases neuron mobility in neuronal cells and leads to abnormal calcium release in cerebellar granule neurons. Knockdown of the ca8 gene results in an abnormal movement pattern in zebrafish.
Our findings provide evidence to support that the impaired protective function of CA8 contributes to human neuropathology, and to suggest that zebrafish can be used as an animal model to study the biological functions of human CA8 in vivo.
碳酸酐酶8(CA8)是α-碳酸酐酶(CAs)的一种同工酶。先前的研究表明,在成人脑中可检测到CA8,在小脑中表达更强烈。据报道,CA8中的单基因突变会导致新的综合征,如共济失调、轻度智力低下或四足步态倾向。
在本研究中,我们检测了CA8在神经元细胞系、小鼠小脑颗粒神经元和斑马鱼中的功能。
我们证明,在星形孢菌素处理下,神经元细胞中CA8的过表达显著降低了细胞死亡。此外,CA8过表达显著提高了神经元细胞和小鼠小脑颗粒神经元的细胞迁移和侵袭能力,这表明CA8可能参与神经元运动和肿瘤发生。通过使用斑马鱼作为动物模型,在通过ca8吗啉代下调CA8后,3dpf斑马鱼胚胎的运动反射受到显著影响。
我们得出结论,CA8过表达使神经元细胞对STS诱导的凋亡应激不敏感,并提高神经元细胞的迁移和侵袭能力。此外,CA8下调会降低神经元细胞中的神经元迁移率,并导致小脑颗粒神经元中钙释放异常。ca8基因敲低导致斑马鱼运动模式异常。
我们的研究结果提供了证据支持CA8保护功能受损导致人类神经病理学,并表明斑马鱼可作为动物模型在体内研究人类CA8的生物学功能。