Preserved neurogenesis in non-demented individuals with AD neuropathology

被引:57
|
作者
Briley, David [1 ]
Ghirardi, Valeria [1 ]
Woltjer, Randy [2 ]
Renck, Alicia [1 ]
Zolochevska, Olga [1 ]
Taglialatela, Giulio [1 ]
Micci, Maria-Adelaide [3 ]
机构
[1] Univ Texas Med Branch, Dept Neurol, Mitchell Ctr Neurodegenerat Dis, Galveston, TX 77555 USA
[2] Oregon Hlth & Sci Univ, Dept Pathol, Portland, OR 97201 USA
[3] Univ Texas Med Branch, Dept Anesthesiol, Galveston, TX 77555 USA
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
关键词
ADULT HIPPOCAMPAL NEUROGENESIS; EPIGENETIC REGULATION; STEM-CELL; HYPERTROPHY; SUFFICIENT; RESISTANCE;
D O I
10.1038/srep27812
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Rare individuals remain cognitively intact despite the presence of neuropathology usually associated with fully symptomatic Alzheimer's disease (AD), which we refer to as Non-Demented with Alzheimer's disease Neuropathology (NDAN). Understanding the involved mechanism(s) of their cognitive resistance may reveal novel strategies to treat AD-related dementia. In the pursuit of this goal, we determined the number of hippocampal neural stem cells (NSCs) and investigated the expression of several miRNAs in NDAN and AD subjects. Laser-capture microdissection of autopsy human hippocampus DG and qRT-PCR miRNA analyses were combined with immunofluorescence in this study. The number of SOX2(+) NSCs in the DG was significantly increased in NDAN individuals as compared to AD subjects. Further, the prevalence of SOX2(+) NSCs was found to correlate with cognitive capacity. Neurogenesis-regulating miRNAs were decreased in NDAN individuals as compared to AD patients. An increased number of NSCs and new neurons in NDAN individuals is associated with a unique expression of regulating miRNAs and strongly support a role of neurogenesis in mediating, in part, the ability of these individuals to resist the pathological burden of AD.
引用
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页数:10
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