Bio-Metal Dyshomeostasis-Associated Acceleration of Aging and Cognitive Decline in Down Syndrome DOI Open Access
Keiichi Ishihara, Eri Kawashita,

Satoshi Akiba

и другие.

Biological and Pharmaceutical Bulletin, Год журнала: 2023, Номер 46(9), С. 1169 - 1175

Опубликована: Авг. 31, 2023

Down syndrome (DS), which is caused by triplication of human chromosome 21 (Hsa21), exhibits some physical signs accelerated aging, such as graying hair, wrinkles and menopause at an unusually young age. Development early-onset Alzheimer's disease, frequently observed in adults with DS, also suggested to occur due aging the brain. Several Hsa21 genes are be responsible for DS. In this review, we summarize these candidate possible molecular mechanisms, discuss related key factors. particular, focus on copper, essential trace element, a factor addition, physiological significance brain copper accumulation cognitive impairment discussed. We herein provide our hypothesis dyshomeostasis-based pathophysiology

Язык: Английский

Epigenetic regulation in adult neural stem cells DOI Creative Commons
Jiajia Shi, Zilin Wang,

Zhijun Wang

и другие.

Frontiers in Cell and Developmental Biology, Год журнала: 2024, Номер 12

Опубликована: Янв. 31, 2024

Neural stem cells (NSCs) exhibit self-renewing and multipotential properties. Adult NSCs are located in two neurogenic regions of adult brain: the ventricular-subventricular zone (V-SVZ) lateral ventricle subgranular dentate gyrus hippocampus. Maintenance differentiation regulated by both intrinsic extrinsic signals that may be integrated through expression some key factors NSCs. A number transcription have been shown to play essential roles transcriptional regulation NSC cell fate transitions brain. Epigenetic regulators also emerged as players NSCs, neural progenitor their differentiated progeny via epigenetic modifications including DNA methylation, histone modifications, chromatin remodeling RNA-mediated regulation. This minireview is primarily focused on regulations during neurogenesis, conjunction with these processes.

Язык: Английский

Процитировано

4

Altered hippocampal neurogenesis in a mouse model of autism revealed by genetic polymorphisms and by atypical development of newborn neurons DOI Creative Commons
Isabel Barón-Mendoza,

Montserrat Mejía-Hernández,

Karina Hernández-Mercado

и другие.

Scientific Reports, Год журнала: 2024, Номер 14(1)

Опубликована: Фев. 26, 2024

Individuals with autism spectrum disorder (ASD) often exhibit atypical hippocampal anatomy and connectivity throughout their lifespan, potentially linked to alterations in the neurogenic process within hippocampus. In this study, we performed an in-silico analysis identify single-nucleotide polymorphisms (SNPs) genes relevant adult neurogenesis C58/J model of idiopathic autism. We found coding non-synonymous (Cn) SNPs 33 involved process, as well 142 associated signature genetic profile neural stem cells (NSC) progenitors. Based on potential predicted by analysis, evaluated number distribution newborn neurons dentate gyrus (DG) young mice. a reduced whole DG, higher proportion early neuroblasts subgranular layer (SGZ), lower morphological maturation signs granule cell (GCL) DG compared C57BL/6J The observed changes may be delay trajectory strain, Cn neurogenesis.

Язык: Английский

Процитировано

3

O-GlcNAc Transferase Congenital Disorder of Glycosylation (OGT-CDG): Potential mechanistic targets revealed by evaluating the OGT interactome DOI Creative Commons
Johnathan M. Mayfield, Naomi L. Hitefield, Ignacy Czajewski

и другие.

Journal of Biological Chemistry, Год журнала: 2024, Номер 300(9), С. 107599 - 107599

Опубликована: Июль 24, 2024

O-GlcNAc transferase (OGT) is the sole enzyme responsible for post-translational modification of on thousands target nucleocytoplasmic proteins. To date, nine variants OGT that segregate with Congenital Disorder Glycosylation (OGT-CDG) have been reported and characterized. Numerous additional associated OGT-CDG, some which are currently undergoing investigation. This disorder primarily presents global developmental delay intellectual disability (ID), alongside other variable neurological features subtle facial dysmorphisms in patients. Several hypotheses aim to explain etiology a prominent hypothesis attributing pathophysiology OGT-CDG mutations segregating this disrupting interactome. The interactome consists proteins, including substrates as well interactors require noncatalytic functions OGT. A key field identify contribute neural-specific phenotype OGT-CDG. In review, we will discuss heterogenous phenotypic seen clinically, biochemical effects use animal models understand disorder. Furthermore, how previously identified causal ID provide mechanistic targets investigation could dysregulated gene expression models. Identifying shared or unique altered pathways impacted patients better understanding potential therapeutic targets.

Язык: Английский

Процитировано

3

Artificial Intelligence and Machine Learning Models for Alzheimer's Disease DOI

Ananya Gambhir,

Ansh Bansal,

Saurabh Rawat

и другие.

Advances in media, entertainment and the arts (AMEA) book series, Год журнала: 2024, Номер unknown, С. 102 - 117

Опубликована: Янв. 10, 2024

Alzheimer's disease is a brain disorder that slowly destroys memory and thinking skills and, eventually, the ability to carry out simplest tasks. In most people with disease, those late-onset type symptoms first appear in their mid-60s. Early-onset occurs between person's 30s mid-60s very rare. common cause of dementia among older adults. Early diagnosis essential for progress more prevailing treatments. Machine learning (ML), branch artificial intelligence, employs variety probabilistic optimization techniques permits PCs gain from vast complex datasets. As result, researchers focus on using machine frequently early stages disease. This project presents review, analysis critical evaluation recent work done detection ML techniques.

Язык: Английский

Процитировано

2

USP9X deubiquitinates TRRAP to promote glioblastoma cell proliferation and migration and M2 macrophage polarization DOI

Bin Mu,

Jiangpeng Jing,

Ruichun Li

и другие.

Naunyn-Schmiedeberg s Archives of Pharmacology, Год журнала: 2024, Номер unknown

Опубликована: Июль 29, 2024

Язык: Английский

Процитировано

0

Oral antioxidant edaravone protects against cognitive deficits induced by chronic hypobaric hypoxia at high altitudes DOI Creative Commons

Yuan-Yuan Ma,

Xin Li, Zhongyuan Yu

и другие.

Translational Psychiatry, Год журнала: 2024, Номер 14(1)

Опубликована: Окт. 3, 2024

Язык: Английский

Процитировано

0

Bio-Metal Dyshomeostasis-Associated Acceleration of Aging and Cognitive Decline in Down Syndrome DOI Open Access
Keiichi Ishihara, Eri Kawashita,

Satoshi Akiba

и другие.

Biological and Pharmaceutical Bulletin, Год журнала: 2023, Номер 46(9), С. 1169 - 1175

Опубликована: Авг. 31, 2023

Down syndrome (DS), which is caused by triplication of human chromosome 21 (Hsa21), exhibits some physical signs accelerated aging, such as graying hair, wrinkles and menopause at an unusually young age. Development early-onset Alzheimer's disease, frequently observed in adults with DS, also suggested to occur due aging the brain. Several Hsa21 genes are be responsible for DS. In this review, we summarize these candidate possible molecular mechanisms, discuss related key factors. particular, focus on copper, essential trace element, a factor addition, physiological significance brain copper accumulation cognitive impairment discussed. We herein provide our hypothesis dyshomeostasis-based pathophysiology

Язык: Английский

Процитировано

0