溶酶体贮积病神经退行性变的统一生物学。

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Inherited Metabolic Disease Pub Date : 2025-01-01 DOI:10.1002/jimd.12833
Anna M Ludlaim, Simon N Waddington, Tristan R McKay
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引用次数: 0

摘要

目前至少有70种典型的溶酶体贮积病(LSD)是由遗传的单基因缺陷引起的。其中,至少30例存在中枢神经系统(CNS)神经变性和重叠病因。底物积累和功能失调的神经元溶酶体是共同的特征,但30种不同基因的变异如何汇聚到这种中心细胞表型尚不清楚。同样未解决的是,神经元溶酶体中多种底物的积累如何导致非常相似的神经退行性结果。相反,为什么许多其他单基因lsd只引起内脏疾病?lsd合并中枢神经退行性变(nLSD)的溶酶体物质积累包括脂褐酶病、粘多糖病、鞘脂病和糖蛋白病。在这里,我们回顾了四类nlsd在基础生物学方面的最新发现,比较和对比了关于疾病机制的新见解和统一趋同的新证据。
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Unifying biology of neurodegeneration in lysosomal storage diseases.

There are currently at least 70 characterised lysosomal storage diseases (LSD) resultant from inherited single-gene defects. Of these, at least 30 present with central nervous system (CNS) neurodegeneration and overlapping aetiology. Substrate accumulation and dysfunctional neuronal lysosomes are common denominator, but how variants in 30 different genes converge on this central cellular phenotype is unclear. Equally unresolved is how the accumulation of a diverse spectrum of substrates in the neuronal lysosomes results in remarkably similar neurodegenerative outcomes. Conversely, how is it that many other monogenic LSDs cause only visceral disease? Lysosomal substance accumulation in LSDs with CNS neurodegeneration (nLSD) includes lipofuscinoses, mucopolysaccharidoses, sphingolipidoses and glycoproteinoses. Here, we review the latest discoveries in the fundamental biology of four classes of nLSDs, comparing and contrasting new insights into disease mechanism with emerging evidence of unifying convergence.

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来源期刊
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease 医学-内分泌学与代谢
CiteScore
9.50
自引率
7.10%
发文量
117
审稿时长
4-8 weeks
期刊介绍: The Journal of Inherited Metabolic Disease (JIMD) is the official journal of the Society for the Study of Inborn Errors of Metabolism (SSIEM). By enhancing communication between workers in the field throughout the world, the JIMD aims to improve the management and understanding of inherited metabolic disorders. It publishes results of original research and new or important observations pertaining to any aspect of inherited metabolic disease in humans and higher animals. This includes clinical (medical, dental and veterinary), biochemical, genetic (including cytogenetic, molecular and population genetic), experimental (including cell biological), methodological, theoretical, epidemiological, ethical and counselling aspects. The JIMD also reviews important new developments or controversial issues relating to metabolic disorders and publishes reviews and short reports arising from the Society''s annual symposia. A distinction is made between peer-reviewed scientific material that is selected because of its significance for other professionals in the field and non-peer- reviewed material that aims to be important, controversial, interesting or entertaining (“Extras”).
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