Publications by authors named "Bing Han Chai"

Elevated iron deposition has been reported in Parkinson's disease (PD). However, the route of iron uptake leading to high deposition in the substantia nigra is unresolved. Here, we show a mechanism in enhanced Fe uptake via S-nitrosylation of divalent metal transporter 1 (DMT1).

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Exposure to divalent metals such as iron and manganese is thought to increase the risk for Parkinson's disease (PD). Under normal circumstances, cellular iron and manganese uptake is regulated by the divalent metal transporter 1 (DMT1). Accordingly, alterations in DMT1 levels may underlie the abnormal accumulation of metal ions and thereby disease pathogenesis.

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Mutations of parkin are a prevalent genetic contributor to familial Parkinson's disease (PD). As a key regulator of protein and mitochondrial homeostasis, parkin plays a pivotal role in maintaining dopaminergic neuronal survival. However, whereas Drosophila parkin null mutants exhibit prominent parkinsonian features, parkin-deficient mice generally lack an overt phenotype.

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The design of the first dual-purpose activity-based probe of monoamine oxidase B (MAO-B) is reported. This probe is highly selective towards MAO-B, even at high MAO-A expression levels, and could sensitively report endogenous MAO-B activities by both in situ proteome profiling and live-cell bioimaging. With a built-in imaging module as part of the probe design, the probe was able to accomplish what all previously reported MAO-B imaging probes failed to do thus far: the live-cell imaging of MAO-B activities without encountering diffusion problems.

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Article Synopsis
  • Stroke is a major health issue causing high rates of death and disability, and recent research highlights the role of Pin1, an enzyme that affects cell growth and apoptosis, in this context.
  • In laboratory studies and mouse models, manipulating Pin1 levels showed that it enhances the stability of Notch1 intracellular domain (NICD1), leading to increased neuron death during ischemic conditions, while reducing Pin1 levels offered protection against stroke damage.
  • The findings suggest that targeting Pin1 could be a potential new treatment strategy for ischemic stroke by inhibiting its role in promoting harmful cell signaling related to stroke-related neuron death.
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