Publications by authors named "Yau Sheng Tsai"

Article Synopsis
  • * The review focuses on innovative approaches for analyzing uremic toxins, like microfluidics, biomarker discovery, and advanced spectroscopy techniques, which aim to enhance toxin removal from patients undergoing dialysis.
  • * It emphasizes the need for early detection of chronic kidney disease and how integrating various scientific disciplines can improve our understanding of toxins and ultimately enhance hemodialysis effectiveness and patient outcomes.
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Article Synopsis
  • Obesity is a major global health issue linked to abnormal fat cell development, with TG-interacting factor 1 (TGIF1) playing a critical role in the differentiation of fat cells.
  • Researchers used CRISPR/Cas9 technology to create preadipocytes lacking TGIF1, which showed no lipid accumulation, highlighting TGIF1's importance in fat cell formation.
  • When TGIF1 was reintroduced in these cells, it spurred lipid accumulation through mechanisms like promoting cell division and regulating specific proteins, potentially offering insights into tackling obesity-related metabolic disorders.
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TG-interacting factor 1 (TGIF1) contributes to the differentiation of murine white preadipocyte and human adipose tissue-derived stem cells; however, its regulation is not well elucidated. Insulin is a component of the adipogenic cocktail that induces ERK signaling. TGIF1 phosphorylation and sustained stability in response to insulin were reduced through the use of specific MEK inhibitor U0126.

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Background: Intradialytic hypotension (IDH) is a common hemodialysis complication causing adverse outcomes. Despite the well-documented associations of ambient temperatures with fluid removal and pre-dialysis blood pressure (BP), the relationship between ambient temperature and IDH has not been adequately studied.

Methods: We conducted a cohort study at a tertiary hospital in southern Taiwan between 1 January 2016 and 31 October 2021.

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Previous studies have shown how adipocytes can modulate the activity of hair follicle stem cells. However, the role of adipocytes in the pathogenesis of androgenetic alopecia (AGA) remains unknown. We aimed to determine signaling pathways related to the adipose tissue changes in the human scalp with AGA through RNA-seq analysis.

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Aims: The aim of this study is to clarify the role of NLRP3 inflammasome in phosphate burden-induced vascular smooth muscle cell (VSMC) calcification.

Main Methods: VSMC calcification was induced using a high concentration of inorganic phosphate. After pharmacological inhibition or genetic silencing of the NLRP3 inflammasome, pyroptosis, or potassium efflux, the cells were examined by RT-qPCR, immunofluorescence, and western blotting to identify the NLRP3-mediated pathway for VSMC calcification.

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Glucose metabolism is known to orchestrate oncogenesis. Whether glucose serves as a signaling molecule directly regulating oncoprotein activity for tumorigenesis remains elusive. Here, we report that glucose is a cofactor binding to methyltransferase NSUN2 at amino acid 1-28 to promote NSUN2 oligomerization and activation.

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Article Synopsis
  • The study explored the potential link between nephrolithiasis (kidney stones) and subclinical coronary artery disease (CAD) in asymptomatic adults, focusing on coronary CT-derived metrics.
  • Results indicated that nearly half of the participants had some level of coronary artery calcium score, with a greater prevalence of nephrolithiasis among those with any calcium score.
  • While nephrolithiasis was associated with higher levels of coronary artery calcification, it did not affect the severity of coronary luminal blockage, suggesting that further research is needed to clarify the relationship between kidney stones and CAD.
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Purpose: Growing evidence have suggested an association between nephrolithiasis and cardiovascular disease (CVD) with unclear mechanism. Oxidized low-density lipoproteins (oxLDL) induces atherosclerosis and was found to be the possible link between these two diseases. Our study aimed to examine the serum, urine and kidney expression of oxLDL in relation to large calcium oxalate (CaOx) renal stone disease.

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Peroxisome proliferator-activated receptor γ (PPARγ) gene mutations in humans and mice lead to whole-body insulin resistance and partial lipodystrophy. It is unclear whether preserved fat depots in partial lipodystrophy are beneficial for whole-body metabolic homeostasis. We analyzed the insulin response and expression of metabolic genes in the preserved fat depots of mice, a familial partial lipodystrophy type 3 (FPLD3) mouse model resulting from a 75% decrease in transcripts.

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The NOD-like receptor family pyrin domain-containing 3 (NLRP3) inflammasome is an oligomeric complex that assembles in response to exogenous signals of pathogen infection and endogenous danger signals of non-microbial origin. When NLRP3 inflammasome assembly activates caspase-1, it promotes the maturation and release of the inflammatory cytokines interleukin-1B and IL-18. Aberrant activation of the NLRP3 inflammasome has been implicated in various diseases, including chronic inflammatory, metabolic, and cardiovascular diseases.

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is a major causative pathogen of nosocomial antibiotic-associated diarrhea and severe colitis. Despite the use of vancomycin and fidaxomicin as standard drugs for the treatment of infection (CDI), clinical relapse rates remain high. Therefore, new alternative therapeutics to treat CDI are urgently required.

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Growth factor signaling plays a pivotal role in diverse biological functions, such as cell growth, apoptosis, senescence, and migration and its deregulation has been linked to various human diseases. Akt kinase is a central player transmitting extracellular clues to various cellular compartments, in turn executing these biological processes. Since the discovery of Akt three decades ago, the tremendous progress towards identifying its upstream regulators and downstream effectors and its roles in cancer has been made, offering novel paradigms and therapeutic strategies for targeting human diseases and cancers with deregulated Akt activation.

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Very preterm infants may require dexamethasone (Dex) for facilitating extubation or treating bronchopulmonary dysplasia. However, Dex may result in disturbance of metabolisms. This study was to investigate the effects of postnatal short course Dex exposure on brown adipose tissue (BAT) in neonatal rats.

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Calcium oxalate (CaOx) is the major constituent of kidney stones. Growing evidence shows a close connection between hyperlipidemia, cardiovascular disease (CVD), and the formation of kidney stones. Owing to their antioxidant properties, statins control hyperlipidemia and may ameliorate CaOx stone formation.

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Background: Several studies have highlighted the incidence of Clostridioides difficile infections (CDIs) in Taiwan and certain ribotypes have been related to severe clinical diseases. A study was conducted to investigate the polymerase chain reaction (PCR) ribotypes and genetic relatedness of clinical C. difficile strains collected from January 2009 to December 2015 at a hospital in northeastern Taiwan.

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Dialysis disequilibrium syndrome (DDS) is a rare complication of dialysis, especially with the general application of preventive strategies. Severe DDS with brain herniation is believed to be fatal. We present a patient presenting with bilateral uncal herniation after receiving two dialysis sessions with low-efficiency settings.

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Calcium (Ca) is an important mediator of multicellular homeostasis and is involved in several diseases. The interplay among the kidney, bone, intestine, and parathyroid gland in Ca homeostasis is strictly modulated by numerous hormones and signaling pathways. The calcium-sensing receptor (CaSR) is a G protein-coupled receptor, that is expressed in calcitropic tissues such as the parathyroid gland and the kidney, plays a pivotal role in Ca regulation.

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Background: Obesity-related cardiovascular risk, end points, and mortality are strongly related to arterial stiffening. Current therapeutic approaches for arterial stiffening are not focused on direct targeting within the vessel. Perivascular adipose tissue (PVAT) surrounding the artery has been shown to modulate vascular function and inflammation.

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Article Synopsis
  • NLRP3 inflammasome activation influenced by metabolic byproducts can lead to inflammation and metabolic diseases, but the mechanisms of host regulation remain unclear.
  • PPARγ, an energy metabolism regulator, appears to reduce inflammation by inhibiting NF-κB and decreasing production of inflammatory markers like IL-1β and IL-18.
  • Using mouse macrophages and human cells, the study found that PPARγ agonists like rosiglitazone can inhibit NLRP3 inflammasome activation and its pathological effects, suggesting PPARγ could be a therapeutic target for inflammatory conditions linked to metabolic issues.
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, an obligate anaerobic gram-positive bacillus, generates spores and is commonly found colonizing the human gut. Patients with infection (CDI) often exhibit clinical manifestations of pseudomembranous colitis or antibiotic-associated diarrhea. Surface layer proteins (SLPs) are the most abundant proteins in the cell wall, suggesting that they might involve in immune recognition.

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: Subjects unable to sustain β-cell compensation develop type 2 diabetes. Early growth response-1 protein (EGR-1), implicated in the regulation of cell differentiation, proliferation, and apoptosis, is induced by diverse metabolic challenges, such as glucose or other nutrients. Therefore, we hypothesized that deficiency of EGR-1 might influence β-cell compensation in response to metabolic overload.

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