Hagiwara A, Hashimoto Y, Niikura T, Ito Y, Terashita K, Kita Y, Nishimoto I, Umezawa K
Department of Applied Chemistry, Keio University, Yokohama, Japan.
Biochem Biophys Res Commun. 2000 Nov 30;278(3):633-9. doi: 10.1006/bbrc.2000.3841.
Since an apolipoprotein E4 (ApoE4) peptide composed of the low-density lipoprotein (LDL) receptor-related protein (LRP)-binding domain [ApoE4(141-149)(2) or ApoE(141-155)(2)] exerts neurotoxicity in primary neurons and neuronal cell lines, it has been controversial whether these effects are mediated by LRP. Here, we examined whether ApoE4(141-149)(2)-induced toxicity is mediated by LRP in a neuronal cell system where ApoE4 toxicity is mediated by LRP: serum-deprived F11 neuronal cells. In these cells, where ApoE4 exerted toxicity by apoptosis in a manner sensitive to both caspase inhibitors and pertussis toxin (PTX), ApoE4(141-149)(2) also caused cell death by apoptosis but in a caspase-inhibitor-resistant, PTX-resistant manner. ApoE4(141-149)(2)-induced death was not inhibited by antisense oligonucleotides to LRP. Therefore, we conclude that ApoE4(141-149)(2) is able to exert neurotoxicity without involving LRP.
由于由低密度脂蛋白(LDL)受体相关蛋白(LRP)结合结构域组成的载脂蛋白E4(ApoE4)肽[ApoE4(141 - 149)(2)或ApoE(141 - 155)(2)]在原代神经元和神经元细胞系中发挥神经毒性作用,这些作用是否由LRP介导一直存在争议。在此,我们在一个ApoE4毒性由LRP介导的神经元细胞系统——血清剥夺的F11神经元细胞中,研究了ApoE4(141 - 149)(2)诱导的毒性是否由LRP介导。在这些细胞中,ApoE4通过凋亡发挥毒性作用,对胱天蛋白酶抑制剂和百日咳毒素(PTX)均敏感,而ApoE4(141 - 149)(2)也通过凋亡导致细胞死亡,但以一种对胱天蛋白酶抑制剂和PTX均耐药的方式。针对LRP的反义寡核苷酸不能抑制ApoE4(141 - 149)(2)诱导的细胞死亡。因此,我们得出结论,ApoE4(141 - 149)(2)能够在不涉及LRP的情况下发挥神经毒性作用。