Publications by authors named "Zhongxiao Fu"

Article Synopsis
  • - Microglia play a key role in regulating cerebral blood flow (CBF), particularly during activities like whisker stimulation or ATP injection, affecting both baseline levels and increases in blood flow.
  • - Depleting microglia reduces activity-dependent blood flow responses, but the body still responds normally to other stimuli like adenosine, indicating a specific function for microglia in this process.
  • - The regulation of CBF by microglia involves the ATP-sensing receptor P2ry12 and the enzyme CD39, which converts extracellular ATP into adenosine, crucial for neurovascular coupling and maintaining healthy blood flow responses.
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Neuroimmune interactions have been studied for decades. Several neurodevelopmental disorders have been associated with immune dysfunction. However, the effects of immune system on neuronal function remain unknown.

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Mechanisms governing how immune cells and their derived molecules impact homeostatic brain function are still poorly understood. Here, we elucidate neuronal mechanisms underlying T cell effects on synaptic function and episodic memory. Depletion of CD4 T cells led to memory deficits and impaired long-term potentiation.

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Background: Although there are many COVID-19 case series studies, few studies report the relationship between variations in blood cell parameters and inflammatory factors and disease severity. This study aims to describe the dynamic trends in COVID-19 blood cell parameters and inflammatory factors.

Methods: Ninety-two patients with confirmed COVID-19 at Jingzhou Central Hospital, Hubei Province, China, between January 23, 2020, and April 10, 2020, were enrolled.

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Background: The global mortality rate for coronavirus disease 2019 (COVID-19) is 3.68%, but the mortality rate for critically ill patients is as high as 50%. Therefore, the exploration of prognostic predictors for patients with COVID-19 is vital for prompt clinical intervention.

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Background: The third fatal coronavirus is the novel coronavirus (SARS-CoV-2) that causes novel coronavirus pneumonia (COVID-19) which first broke out in December 2019. Patients will develop rapidly if there is no any intervention, so the risk identification of severe patients is critical. The aim of this study was to investigate the characteristics and rules of hematology changes in patients with COVID-19, and to explore the possibility differentiating moderate and severe patients using conventional hematology parameters or combined parameters.

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The nature of fluid dynamics within the brain parenchyma is a focus of intensive research. Of particular relevance is its participation in diseases associated with protein accumulation and aggregation in the brain, such as Alzheimer's disease (AD). The meningeal lymphatic vessels have recently been recognized as an important player in the complex circulation and exchange of soluble contents between the cerebrospinal fluid (CSF) and the interstitial fluid (ISF).

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Mitochondrial flashes (mitoflashes) are recently discovered excitable mitochondrial events in many cell types. Here we investigate their occurrence in the context of structural long-term potentiation (sLTP) at hippocampal synapses. At dendritic spines stimulated by electric pulses, glycine, or targeted glutamate uncaging, induction of sLTP is associated with a phasic occurrence of local, quantized mitochondrial activity in the form of one or a few mitoflashes, over a 30-min window.

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Article Synopsis
  • HCV infection leads to significant changes in the N-glycan profiles of liver cells, resulting in elevated levels of fucosylated, sialylated, and complex N-glycans.
  • The study employed various methods like mass spectrometry and lectin assays to identify changes in glycosylated proteins, notably increased fucosylated modifications of annexin A2 and heat shock protein 90 beta (HSP90B1).
  • FUT8, a glycosyltransferase, was found to be up-regulated in HCV-infected cells, suggesting its key role in the observed glycan alterations and highlighting potential avenues for future diagnostics and therapies related to HCV.
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Excessive glutamate release causes overactivation of N-methyld-aspartate receptors (NMDARs), leading to excitatory neuronal damage in cerebral ischemia. Hydroxysafflor yellow A (HSYA), a compound extracted from Carthamus tinctorius L., has been reported to exert a neuroprotective effect in many pathological conditions, including brain ischemia.

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