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BDNF Val66Met 多态性(rs6265)增强了 rs6265 敲入大鼠中多巴胺神经元移植物的疗效和副作用倾向。

The BDNF Val66Met polymorphism (rs6265) enhances dopamine neuron graft efficacy and side-effect liability in rs6265 knock-in rats.

机构信息

Department of Translational Neuroscience, College of Human Medicine, Michigan State University, Grand Rapids, MI 49503, USA.

Department of Translational Neuroscience, College of Human Medicine, Michigan State University, Grand Rapids, MI 49503, USA; Hauenstein Neuroscience Center, Mercy Health Saint Mary's, Grand Rapids, Michigan 49503, USA.

出版信息

Neurobiol Dis. 2021 Jan;148:105175. doi: 10.1016/j.nbd.2020.105175. Epub 2020 Nov 11.

Abstract

Prevalent in approximately 20% of the worldwide human population, the rs6265 (also called 'Val66Met') single nucleotide polymorphism (SNP) in the gene for brain-derived neurotrophic factor (BDNF) is a common genetic variant that can alter therapeutic responses in individuals with Parkinson's disease (PD). Possession of the variant Met allele results in decreased activity-dependent release of BDNF. Given the resurgent worldwide interest in neural transplantation for PD and the biological relevance of BDNF, the current studies examined the effects of the rs6265 SNP on therapeutic efficacy and side-effect development following primary dopamine (DA) neuron transplantation. Considering the significant reduction in BDNF release associated with rs6265, we hypothesized that rs6265-mediated dysfunctional BDNF signaling contributes to the limited clinical benefit observed in a subpopulation of PD patients despite robust survival of grafted DA neurons, and further, that this mutation contributes to the development of aberrant graft-induced dyskinesias (GID). To this end, we generated a CRISPR knock-in rat model of the rs6265 BDNF SNP to examine for the first time the influence of a common genetic polymorphism on graft survival, functional efficacy, and side-effect liability, comparing these parameters between wild-type (Val/Val) rats and those homozygous for the variant Met allele (Met/Met). Counter to our hypothesis, the current research indicates that Met/Met rats show enhanced graft-associated therapeutic efficacy and a paradoxical enhancement of graft-derived neurite outgrowth compared to wild-type rats. However, consistent with our hypothesis, we demonstrate that the rs6265 genotype in the host rat is strongly linked to development of GID, and that this behavioral phenotype is significantly correlated with neurochemical signatures of atypical glutamatergic neurotransmission by grafted DA neurons.

摘要

在全球人类人口中约有 20%存在这种情况,脑源性神经营养因子(BDNF)基因中的 rs6265(也称为“Val66Met”)单核苷酸多态性(SNP)是一种常见的遗传变异,可改变帕金森病(PD)患者的治疗反应。携带变异 Met 等位基因会导致 BDNF 的活性依赖性释放减少。鉴于全球对 PD 神经移植的兴趣重新燃起,以及 BDNF 的生物学相关性,目前的研究检查了 rs6265 SNP 对原发性多巴胺(DA)神经元移植后治疗效果和副作用发展的影响。考虑到与 rs6265 相关的 BDNF 释放显著减少,我们假设 rs6265 介导的 BDNF 信号功能障碍导致尽管移植的 DA 神经元存活良好,但在一小部分 PD 患者中观察到有限的临床获益,并且进一步认为这种突变导致异常移植诱导的运动障碍(GID)的发展。为此,我们生成了 rs6265 BDNF SNP 的 CRISPR 敲入大鼠模型,首次检查了常见遗传多态性对移植物存活、功能疗效和副作用易感性的影响,在野生型(Val/Val)大鼠和纯合变异 Met 等位基因(Met/Met)大鼠之间比较这些参数。与我们的假设相反,目前的研究表明,与野生型大鼠相比,Met/Met 大鼠显示出增强的与移植物相关的治疗效果和移植源性神经突生长的反常增强。然而,与我们的假设一致,我们证明宿主大鼠中的 rs6265 基因型与 GID 的发展密切相关,并且这种行为表型与移植的 DA 神经元的非典型谷氨酸能神经传递的神经化学特征显著相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3eb/7855552/0ecfa3368611/nihms-1649084-f0001.jpg

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