Kunimoto M, Suzuki T
Environmental Health Sciences Division, The National Institute for Environmental Studies, Tsukuba, Ibaraki, Japan.
Neuroreport. 1995 Dec 15;6(18):2545-8. doi: 10.1097/00001756-199512150-00023.
Brain-specific isoforms of ankyrin, 440 kDa and 220 kDa ankyrinB, which are generated from a single gene by alternative splicing of pre-mRNA, are both expressed in human neuroblastoma NB-1 cells and the expression of the larger isoform is increased upon induction of neurite outgrowth. Exposure to methylmercury, a potent neurotoxic substance, at a sublethal dose induced dramatic retraction of neurites in NB-1 cells. Concomitantly, synthesis of 440 kDa ankyrinB polypeptide and mRNA were selectively attenuated in methylmercury-treated cells, while the 220 kDa isoform was not affected. These results indicate that the expression of 440 kDa ankyrinB is intimately associated not only with the neurite outgrowth but also with neurite retraction in neuronal cells, and is regulated at mRNA level.
锚蛋白的脑特异性同工型,即440 kDa和220 kDa的锚蛋白B,由一个基因通过前体mRNA的可变剪接产生,二者均在人神经母细胞瘤NB-1细胞中表达,且在诱导神经突生长时,较大同工型的表达增加。暴露于亚致死剂量的强效神经毒性物质甲基汞会诱导NB-1细胞中的神经突急剧回缩。与此同时,在甲基汞处理的细胞中,440 kDa锚蛋白B多肽和mRNA的合成被选择性减弱,而220 kDa同工型则不受影响。这些结果表明,440 kDa锚蛋白B的表达不仅与神经突生长密切相关,还与神经元细胞中的神经突回缩密切相关,并且在mRNA水平受到调控。