Publications by authors named "Kazuya Yamada"

Precise regulation of organ size and position is crucial for optimal organ function. Since the swim bladder is primarily responsible for buoyancy in teleosts, early development and subsequent inflation of the swim bladder should be appropriately controlled with the body growth. However, the underlying mechanism remains unclear.

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The vertebral column is a characteristic structure of vertebrates. Genetic studies in mice have shown that Hox-mediated patterning plays a key role in specifying discrete anatomical regions of the vertebral column. Expression pattern analyses in several vertebrate embryos have provided correlative evidence that the anterior boundaries of Hox expression coincide with distinct anatomical vertebrae.

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The dorsal and anal fins can vary widely in position and length along the anterior-posterior axis in teleost fishes. However, the molecular mechanisms underlying the diversification of these fins remain unknown. Here, we used genetic approaches in zebrafish and medaka, in which the relative positions of the dorsal and anal fins are opposite, to demonstrate the crucial role of genes in the patterning of the teleost posterior body, including the dorsal and anal fins.

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Article Synopsis
  • An 8-year-old boy presented with cubitus varus deformity and an olecranon fracture after a fall, initially treated with closed reduction and casting but later required corrective osteotomy due to lack of remodeling.
  • After 2.5 years post-surgery, the boy showed little change in carrying angle and varus angulation of the affected arm compared to the other side, with no pain or limited motion.
  • The study emphasizes the importance of early accurate reduction and possibly internal fixation to prevent complications like cubitus varus deformity, highlighting corrective osteotomy as an effective treatment option.
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Approximately 1.14 billion smokers worldwide are at risk of developing tumors, cardiovascular diseases and respiratory diseases. Smoking cessation is the first choice of health care; however, the disease should be attenuated in individuals who never stop smoking, which escalates medical costs.

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β-caryophyllene (BCP) is a volatile bicyclic sesquiterpenoid found in essential oils obtained from several spices such as black pepper, oregano, basil, rosemary, cinnamon, and clove. BCP is a selective agonist of cannabinoid receptor 2 (CB2 receptor), and orally administered BCP exhibits various biological activities, including anti-inflammatory, antioxidant, and neuroprotective effects. However, it is still unclear how volatile BCP affects living organisms.

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Multiple subcutaneous extensor tendon ruptures in more than the ulnar three fingers sometimes occur in patients with rheumatoid arthritis accompanied by wrist deformity. In these situations, the flexor digitorum superficialis tendon of the middle finger (the FDS3 tendon) and that of the ring finger (the FDS4 tendon) are used for the transferred tendon (modified Boyes' procedure). Here, we treated two patients with rheumatoid arthritis, whose extensor tendons of more than three fingers were ruptured, using the modified Boyes' procedure.

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In this study, we fabricated two different microneedles (MNs) - semi-hollow and bird-bill - to overcome the limitations of solid and coated MNs, respectively. The two MN arrays were developed using a general injection molding process to obtain high-quality MNs with uniform shape. The semi-hollow and bird-bill MNs could penetrate the micropores of swine skin up to depths of 178.

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Vertebrate Hox clusters are comprised of multiple Hox genes that control morphology and developmental timing along multiple body axes. Although results of genetic analyses using Hox-knockout mice have been accumulating, genetic studies in other vertebrates have not been sufficient for functional comparisons of vertebrate Hox genes. In this study, we isolated all of the seven hox cluster loss-of-function alleles in zebrafish using the CRISPR-Cas9 system.

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Members of the enhancer of split- and hairy-related protein (SHARP) family, SHARP-1 and SHARP-2, are basic helix-loop-helix transcriptional repressors and belong to the clock genes. In this study, an effect of retinoic acid (RA) on the SHARP family gene expression in the differentiated cells was examined. RA rapidly and temporarily induced the SHARP-2 mRNA expression in hepatic H4IIE cells.

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Article Synopsis
  • Melatonin is known to play important roles in various bodily functions, but its influence on liver glucose metabolism, specifically the gene expression of the enzyme PEPCK, was unclear until this study.
  • The study found that melatonin increased PEPCK mRNA levels in liver cells and that this effect was enhanced by dexamethasone but inhibited by insulin, with the involvement of specific signaling pathways.
  • The research concluded that melatonin activates PEPCK gene expression through the ERK1/2 pathway at the transcriptional level, requiring new protein synthesis for this process.
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The rat genes encode insulin-inducible transcriptional repressors. A longevity gene, encodes protein deacetylase. These play an important role in regulating hepatic glucose metabolism.

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In the zebrafish segmentation clock, hairy/enhancer of split-related genes her1, her7, and hes6 encodes components of core oscillators. Since the expression of cyclic genes proceeds rapidly in the presomitic mesoderm (PSM), these hairy-related mRNAs are subject to strict post-transcriptional regulation. In this study, we demonstrate that inhibition of the CCR4-NOT deadenylase complex lengthens poly(A) tails of hairy-related mRNAs and increases the amount of these mRNAs, which is accompanied by defective somite segmentation.

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We performed whole exome or genome sequencing in eight multiply affected families with ostensibly isolated congenital anosmia. Hypothesis-free analyses based on the assumption of fully penetrant recessive/dominant/X-linked models obtained no strong single candidate variant in any of these families. In total, these eight families showed 548 rare segregating variants that were predicted to be damaging, in 510 genes.

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Leukocyte telomere length and serum levels of high-molecular-weight adiponectin and dehydroepiandrosterone-sulfate (DHEA-S) were assessed in association with nutrition and performance status (PS) in Japanese centenarians. Twenty-three centenarians (five men, 18 women) were classified according to their PS 1 (nearly fully ambulatory, = 2), 2 (in bed less than 50% of daytime, = 10), 3 (in bed greater than 50%, = 6), and 4 (completely bedridden, = 5). Leukocyte telomere length was determined by the hybridization protection assay, and the adiponectin and DHEA-S levels were measured by chemiluminescent enzyme immunoassay.

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Article Synopsis
  • * Patients were randomly assigned to a control group or one of three treatment groups receiving different dosages of BTX-B (250, 1,000, or 2,000 U).
  • * Results showed that the higher doses (1,000 and 2,000 U) significantly reduced pain and the severity of Raynaud's symptoms, with sustained improvement for up to 16 weeks and fewer digital ulcers, all without serious side effects.
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The rat enhancer of split- and hairy-related protein-2 (SHARP-2) is an insulin-inducible transcription factor which represses transcription of the rat phosphoenolpyruvate carboxykinase gene. In this study, a regulatory mechanism of the SHARP-2 mRNA level by insulin was analyzed. Insulin rapidly induced the level of SHARP-2 mRNA.

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Resistin is a cytokine inducing insulin resistance in mice. We previously identified single nucleotide polymorphisms (SNPs) at -420 (rs1862513) and -358 (rs3219175) located in the human resistin gene () promoter as strong determinants for circulating resistin in the Japanese population. The objective was to identify additional functional variants for circulating resistin.

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Raynaud's phenomenon is frequently observed in systemic sclerosis (SSc) patients, and cold- or stress-induced norepinephrine (NE) has been speculated to be associated with vasoconstriction. Objective was to elucidate the role of NE in fibrosis in SSc. IL-6 is a potent stimulator of collagen production in fibroblasts.

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Atypical progeroid syndrome (APS), including atypical Werner syndrome (AWS), is a disorder of premature ageing caused by mutation of the lamin A gene, the same causal gene involved in Hutchinson-Gilford syndrome (HGS). We previously reported the first Japanese case of APS/AWS with a LMNA mutation (p.D300N).

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  • The study explores how MFG-E8, an angiogenic factor secreted by pericytes, contributes to melanoma tumor growth, potentially counteracting anti-VEGF therapies.
  • Researchers found that bone marrow-derived mesenchymal stromal cells (MSC) express high levels of MFG-E8, and experiments showed that tumors grown with MSC lacking MFG-E8 (KO) had reduced growth and fewer associated immune cells.
  • The results indicate that MFG-E8 enhances tumor angiogenesis by increasing the expression of other growth factors (VEGF and ET-1) in MSC and promoting the polarization of M2 macrophages, which are associated with tumor support.
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Ischaemia-reperfusion (I/R) is involved in the development of various organ diseases. There has been increasing evidence that cutaneous I/R injury is associated with the pathogenesis of pressure ulcers (PUs), especially at the early stage presenting as non-blanchable erythema. However, there is no evidence-based treatment for early-stage PUs.

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The 5'-AMP-activated protein kinase (AMPK) functions as a cellular energy sensor. 5-Aminoimidazole-4-carboxyamide-1-β-D-ribofranoside (AICAR) is a chemical activator of AMPK. In the liver, AICAR suppresses expression of thephosphoenolpyruvate carboxykinase(PEPCK) gene.

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