Heijink E, Scholten S W, Bolhuis P A, de Wolff F A
Coronel Institute for Occupational and Environmental Health, Academic Medical Center, University of Amsterdam, P.O. Box 22700, 1100 DE, Amsterdam, The Netherlands.
Chem Biol Interact. 2000 Dec 15;129(3):231-47. doi: 10.1016/s0009-2797(00)00207-6.
2,5-Hexanedione (2,5-HD), the neurotoxic metabolite of n-hexane, can structurally modify neurofilaments (NF) by pyrrole adduct formation and subsequent covalent cross-linking. 2,5-HD also induces accumulations of NF within the pre-terminal axon. We examined whether exposure of NF to 2,5-HD affected NF degradation. Two different models were used: (1) NF-enriched cytoskeletons isolated from human sciatic nerve were incubated with 2,5-HD in vitro and (2) differentiated human neuroblastoma cells (SK-N-SH) were exposed to 2, 5-HD in culture prior to isolation of cytoskeletal proteins. The cytoskeletal preparations were subsequently incubated with calpain II. The amount of NF-H and NF-L remaining after proteolysis was determined by SDS-PAGE and quantitative immunoblotting. NF-M proteolysis could not be quantified. Incubation of sciatic nerve cytoskeletal preparations with 2,5-HD resulted in cross-linking of all three NF proteins into high molecular weight (HMW) material with a range of molecular weights. Proteolysis of the NF-H and NF-L polypeptides was not affected by 2,5-HD-exposure. Degradation of the HMW material containing NF-H or NF-L was retarded when comparing with degradation of the NF-H and NF-L polypeptides, respectively, from control samples, but not as compared to the corresponding NF polypeptides from 2,5-HD-treated samples. Exposure of SK-N-SH cells to 2,5-HD also resulted in considerable cross-linking of NF. No differences were found between the proteolytic rates of NF-L and NF-H from exposed cells as compared with those subunits from control cells. Moreover, degradation of cross-linked NF-H was not different from monomeric NF-H. In conclusion, whether 2,5-HD affects calpain-mediated degradation of cross-linked NF proteins will depend on which model better reflects NF cross-linking as occurring in 2, 5-HD-induced axonopathy. However, with both models it was demonstrated that exposure of NF proteins to 2,5-HD without subsequent cross-linking is not adequate to inhibit NF proteolysis in vitro by added calpain.
正己烷的神经毒性代谢产物2,5 -己二酮(2,5 - HD)可通过形成吡咯加合物并随后进行共价交联在结构上修饰神经丝(NF)。2,5 - HD还会诱导终末前轴突内NF的积聚。我们研究了NF暴露于2,5 - HD是否会影响NF的降解。使用了两种不同的模型:(1)从人坐骨神经中分离出的富含NF的细胞骨架在体外与2,5 - HD孵育,以及(2)分化的人神经母细胞瘤细胞(SK - N - SH)在分离细胞骨架蛋白之前在培养物中暴露于2,5 - HD。随后将细胞骨架制剂与钙蛋白酶II孵育。通过SDS - PAGE和定量免疫印迹法测定蛋白水解后剩余的NF - H和NF - L的量。无法对NF - M的蛋白水解进行定量。坐骨神经细胞骨架制剂与2,5 - HD孵育导致所有三种NF蛋白交联成一系列分子量的高分子量(HMW)物质。NF - H和NF - L多肽的蛋白水解不受2,5 - HD暴露的影响。与对照样品中NF - H和NF - L多肽的降解相比,含有NF - H或NF - L的HMW物质的降解分别受到抑制,但与2,5 - HD处理样品中的相应NF多肽相比则不然。SK - N - SH细胞暴露于2,5 - HD也导致NF大量交联。与对照细胞的那些亚基相比,暴露细胞中NF - L和NF - H的蛋白水解速率没有差异。此外,交联的NF - H的降解与单体NF - H没有差异。总之,2,5 - HD是否会影响钙蛋白酶介导的交联NF蛋白的降解将取决于哪种模型能更好地反映2,5 - HD诱导的轴突病中发生的NF交联。然而,在两种模型中均证明,NF蛋白暴露于2,5 - HD而不随后交联不足以在体外抑制添加的钙蛋白酶对NF的蛋白水解。