The Genetic Background of the Immunological and Inflammatory Aspects of Progressive Supranuclear Palsy DOI Open Access
Piotr Alster, Natalia Madetko‐Alster

International Journal of Molecular Sciences, Год журнала: 2025, Номер 26(9), С. 3927 - 3927

Опубликована: Апрель 22, 2025

Progressive supranuclear palsy (PSP) is a neurodegenerative disease, classified as an atypical Parkinsonian syndrome, that has been pathologically and clinically defined. The histopathological aspects of the disease include tufted astrocytes, while clinical features involve oculomotor dysfunction, postural instability, akinesia, cognitive impairment, language difficulties. Although PSP generally considered sporadic interest growing in its genetics, with contemporary research focusing on familial backgrounds neuroinflammation. Indeed, microglial activation other inflammatory mechanisms pathogenesis have extensively analyzed using genetic examinations to identify factors impacting neurodegeneration. As such, this review aims elaborate recent findings field.

Язык: Английский

Bassoon, Presynaptic Scaffolding Protein: Narrative Review in Health and Disease DOI

Ahamed P. Kaladiyil,

Prashanth Lingappa Kukkle

European Journal of Neuroscience, Год журнала: 2025, Номер 61(5)

Опубликована: Март 1, 2025

ABSTRACT The release of synaptic vesicles (SVs) at the junction is a complex process involving various specialized proteins that work in unison. Among these, Bassoon has emerged as significant protein, particularly noted for its association with neurological and aging‐related diseases. Due to structural functional roles, become focus recent research, especially understanding implications neurodegenerative psychiatric disorders. In this narrative review, we explore Bassoon's structure, function, role across spectrum Neurotransmission tightly regulated relies on structures within presynaptic terminal, such active zone (AZ), precisely control SV response incoming signals. AZ comprises network large, multidomain proteins, playing crucial arrangement. facilitates tethering reloading SVs, ensuring responsiveness high‐frequency signals, while also maintaining proteostasis presynapse. This involves orchestrating localization essential neuronal development plasticity. large size unique features enable it interact regulate function multiple making integral functioning. Variants gene have been linked variety conditions, including Progressive Supranuclear Palsy, system atrophy (MSA), epilepsy, schizophrenia, bipolar disorder, Parkinson's disease. review delves into pivotal preserving integrity how disruptions functions may contribute these

Язык: Английский

Процитировано

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The Genetic Background of the Immunological and Inflammatory Aspects of Progressive Supranuclear Palsy DOI Open Access
Piotr Alster, Natalia Madetko‐Alster

International Journal of Molecular Sciences, Год журнала: 2025, Номер 26(9), С. 3927 - 3927

Опубликована: Апрель 22, 2025

Progressive supranuclear palsy (PSP) is a neurodegenerative disease, classified as an atypical Parkinsonian syndrome, that has been pathologically and clinically defined. The histopathological aspects of the disease include tufted astrocytes, while clinical features involve oculomotor dysfunction, postural instability, akinesia, cognitive impairment, language difficulties. Although PSP generally considered sporadic interest growing in its genetics, with contemporary research focusing on familial backgrounds neuroinflammation. Indeed, microglial activation other inflammatory mechanisms pathogenesis have extensively analyzed using genetic examinations to identify factors impacting neurodegeneration. As such, this review aims elaborate recent findings field.

Язык: Английский

Процитировано

0