Publications by authors named "Aya Miyauchi"

Article Synopsis
  • Chronic liver diseases, such as metabolic dysfunction-associated steatohepatitis (MASH), are increasingly prevalent and linked to severe fibrosis, yet effective treatments are lacking.
  • The study explored the role of the protein hydrogen peroxide-inducible clone-5 (Hic-5) in liver fibrosis and its expression in human tissues, particularly in relation to MASH, while also testing therapeutic antisense oligonucleotides (ASOs) targeting Hic-5 in a mouse model.
  • Results indicated that Hic-5 is significantly associated with the progression of liver fibrosis and that ASOs can effectively reduce Hic-5 expression, providing a potential therapeutic strategy for advanced liver diseases.
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Osteoarthritis (OA) is the most common joint disease associated with articular cartilage destruction. Matrix metalloproteinase-13 (MMP-13) has an essential role in OA pathogenesis by degradation of collagen II, a major component of articular cartilage. Hydrogen peroxide-inducible clone-5 (Hic-5; TGFB1I1), a transforming growth factor-β-inducible mechanosensor, has previously been reported to promote OA pathogenesis by upregulating MMP-13 expression in mouse osteoarthritic lesions.

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Accumulated evidence suggests that activated pancreatic stellate cells (PSCs) serve as the main source of the extracellular matrix proteins accumulated under the pathological conditions leading to pancreatic fibrosis in chronic pancreatitis (CP). However, little is known about the mechanisms of PSC activation. PSCs have morphologic and functional similarities to hepatic stellate cells, which are activated by hydrogen peroxide-inducible clone-5 (Hic-5), a TGF-β1-induced protein.

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Excessive mechanical stress is a major cause of knee osteoarthritis. However, the mechanism by which the mechanical stress begets osteoarthritis development remains elusive. Hydrogen peroxide-inducible clone-5 (Hic-5; TGFβ1i1), a TGF-β inducible focal adhesion adaptor, has previously been reported as a mediator of mechanotransduction.

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Carcinoma-associated fibroblasts (CAFs) influence tumor initiation, progression, and metastasis within the tumor-associated stroma. This suggests that CAFs would be a potential target for tumor therapy. Here we found that Hydrogen peroxide-inducible clone-5 (Hic-5), also named transforming growth factor beta-1-induced transcript 1 protein (Tgfb1i1), was strongly induced in CAFs found in human colorectal cancer.

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Article Synopsis
  • * Hic-5 was found to be present in ECs but not in monocytes; its deficiency reduced monocyte adhesion to aortas and decreased the formation of atherosclerotic lesions by 60% in mouse models prone to atherosclerosis.
  • * Overexpression of Hic-5 in cultured human ECs enhanced the formation of microvilli-like structures, improving monocyte adhesion, highlighting its significant role in the development of atherosclerosis.
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Hydrogen peroxide-inducible clone-5 (Hic-5) is a focal adhesion scaffold protein primarily expressed in vascular and visceral smooth muscle cells. We recently generated mice lacking Hic-5, which grew with no apparent abnormality (Kim-Kaneyama J, et al. J Mol Cell Cardiol.

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Multiple lines of evidence from molecular studies indicate that individual taste qualities are encoded by distinct taste receptor cells. In contrast, many physiological studies have found that a significant proportion of taste cells respond to multiple taste qualities. To reconcile this apparent discrepancy and to identify taste cells that underlie each taste quality, we investigated taste responses of individual mouse fungiform taste cells that express gustducin or GAD67, markers for specific types of taste cells.

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