Mann D M, Pickering-Brown S M, Siddons M A, Iwatsubo T, Ihara Y, Asami-Odaka A, Suzuki N
Department of Pathological Sciences, University of Manchester, UK.
Neurosci Lett. 1995 Aug 18;196(1-2):105-8. doi: 10.1016/0304-3940(95)11860-y.
The extent of deposition of amyloid beta protein (A beta) was investigated in 20 elderly patients with Down's syndrome, using the end-specific monoclonal antibodies BC05 and BA27 to detect the presence of A beta 42(43) and A beta 40 (respectively), and related to apolipoprotein E (ApoE) genotype. No significant differences in the amount of A beta deposited in the brain, either as A beta 42(43) or A beta 40, were noted in patients possessing an ApoE E4 allele, compared to those without. Patients with an ApoE E4 allele in general died at an earlier age than those with only ApoE E3 alleles, the latter in turn being outlived by those with an ApoE E2 allele. In Down's syndrome therefore, ApoE may influence the timing of onset, or the rate of progression, of disease but without affecting the type or total amount of pathology accumulated.
使用末端特异性单克隆抗体BC05和BA27分别检测β淀粉样蛋白(Aβ)42(43)和Aβ40的存在情况,对20名老年唐氏综合征患者的Aβ沉积程度进行了研究,并与载脂蛋白E(ApoE)基因型相关联。与不携带ApoE E4等位基因的患者相比,携带该等位基因的患者大脑中以Aβ42(43)或Aβ40形式沉积的Aβ量没有显著差异。一般来说,携带ApoE E4等位基因的患者比仅携带ApoE E3等位基因的患者死亡年龄更早,而后者又比携带ApoE E2等位基因的患者寿命短。因此,在唐氏综合征中,ApoE可能会影响疾病的发病时间或进展速度,但不影响积累的病理类型或总量。