Publications by authors named "Keita Maki"

Objectives: While esophageal varices (EVs) are typically treated endoscopically, other options such as interventional radiology or surgical treatment are considered when endoscopic treatment is challenging. Pipeline EVs are difficult to treat endoscopically due to their large diameter, and currently, no specific treatment guidelines have been established.

Methods: We reviewed cases of pipeline EVs treated at our hospital and analyzed previously reported cases to collect evidence for the formulation of treatment guidelines.

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Background: Multiple factors are involved in the pathogenesis of primary biliary cholangitis (PBC), a chronic cholestatic liver disease, characterized by intrahepatic cholangiopathy. In particular, studies have suggested that environmental factors such as the presence of granulomas in the portal vein region are important for the development of PBC. This study aimed to comprehensively analyze and identify foreign-derived antigens in PBC liver tissue to confirm their involvement in PBC pathogenesis.

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Article Synopsis
  • Cholestatic liver diseases involve inflammation and fibrosis around bile ducts, but the mechanisms behind this pathology are not fully understood, prompting investigation into the role of extracellular vesicles (EVs).
  • Researchers stimulated biliary epithelial cells with bile acids and found that EVs released from these cells could activate inflammatory responses in macrophages and promote fibrosis in other cell types.
  • The study identified specific proteins in the stimulated EVs that were linked to increased production of inflammatory cytokines and fibrotic markers, suggesting that these EVs contribute to the progression of cholestatic liver diseases.
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Although liver regeneration has been extensively studied, the effects of bile-derived extracellular vesicles (bile EVs) on hepatocytes has not been elucidated. We examined the influence of bile EVs, collected from a rat model of 70% partial hepatectomy (PH), on hepatocytes. We produced bile-duct-cannulated rats.

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