11 results on '"Nakamura, Yukio"'
Search Results
2. Buchsbaumness of ordinary powers of two-dimensional square-free monomial ideals
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Minh, Nguyên Công and Nakamura, Yukio
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BUCHSBAUM rings , *DIMENSIONAL analysis , *IDEALS (Algebra) , *POLYNOMIALS , *MATHEMATICAL complexes , *HOMOLOGY theory - Abstract
Abstract: Let be a polynomial ring. Let I be a Stanley–Reisner ideal in S of a pure simplicial complex of dimension one. In this paper, we study the Buchsbaum property of for any integer . Our first purpose is giving a characterization of Ext-modules for any monomial ideal J, where , in terms of certain simplicial complexes. Then we consider the Buchsbaum property of . The main tool to check the Buchsbaumness is the surjectivity criterion. We see the behavior of the canonical map from to from the view point of reduced cohomology groups of simplicial complexes. [ABSTRACT FROM AUTHOR]
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- 2011
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3. Wnt16 regulates osteoclast differentiation in conjunction with Wnt5a.
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Kobayashi, Yasuhiro, Thirukonda, Gnanasagar J., Nakamura, Yukio, Koide, Masanori, Yamashita, Teruhito, Uehara, Shunsuke, Kato, Hiroyuki, Udagawa, Nobuyuki, and Takahashi, Naoyuki
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WNT proteins , *OSTEOCLASTS , *CELL differentiation , *CATENINS , *CELLULAR signal transduction , *OSTEOCLASTOGENESIS - Abstract
The canonical Wnt/β-catenin signaling pathway in osteoblast-lineage cells inhibits osteoclastogenesis through the expression of osteoprotegerin (Opg), a decoy receptor of receptor activator of Nf-κb (Rank) ligands. Wnt5a, a typical non-canonical Wnt ligand, enhances the expression of Rank in osteoclast precursors, which, in turn, promotes the Rank ligand (Rankl)-induced formation of osteoclasts. In contrast, Wnt16 and Wnt4 have been shown to inhibit the Rankl-induced formation of osteoclasts through non-canonical Wnt signals. However, the relationships among these Wnt ligands in osteoclastogenesis remained to be elucidated. We herein showed that Wnt16, but not Wnt4, inhibited the Rankl-induced osteoclastogenesis in bone marrow-derived macrophage (BMM) cultures. Wnt3a and Wnt4 inhibited the 1α,25-dihydroxy vitamin D 3 (1,25D 3 )-induced osteoclastogenesis in co-cultures prepared from wild-type mice, but not in those from Opg –/– nice. Wnt16 inhibited the 1,25D 3 -induced formation of osteoclasts in both wild-type and Opg –/– co-cultures. Wnt16, Wnt4, and Wnt3a failed to inhibit the pit-forming activity of osteoclasts. Wnt16 failed to inhibit the Wnt5a-induced expression of Rank in osteoclast precursors. In contrast, Wnt5a abrogated the inhibitory effects of Wnt16 on Rankl-induced osteoclastogenesis. These results suggested that Wnt16 inhibited osteoclastogenesis, but not the function of osteoclasts and that Wnt16, an inhibitory Wnt ligand for osteoclastogenesis, regulates bone resorption in conjunction with Wnt5a. [ABSTRACT FROM AUTHOR]
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- 2015
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4. Ascorbic acid predominantly kills cancer stem cell-like cells in the hepatocellular carcinoma cell line Li-7 and is more effective at low cell density and in small spheroids.
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Seyama, Yusuke, Sudo, Kazuhiro, Yamada, Takeshi, Tsuchiya, Kiichiro, and Nakamura, Yukio
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CANCER stem cells , *VITAMIN C , *HEPATOCELLULAR carcinoma , *CELL lines , *REACTIVE oxygen species , *CELL populations , *CELL culture - Abstract
The development of therapies that target cancer stem cells (CSCs) is an important challenge in cancer research. The antioxidant system is enhanced in CSCs, which may lead to resistance to existing therapies. Ascorbic acid (AA) has the potential to act as both an antioxidant and a pro-oxidant agent, but its effects on CSCs are a subject of current research. Here, we investigated the effect of AA focusing specifically on CSCs with the hepatocellular carcinoma cell line Li-7. The Li-7 cell line is heterogenous consisting of CD166- and CD166+ cells; CD166- cells include CSC-like cells (CD13+CD166- cells) and CD13−CD166- cells that can revert to CD13+CD166- cells. The addition of AA to the culture medium caused cell death in both cell populations in CD166- cells in a concentration dependent manner. In contrast, AA administration had a limited effect on CD166+ non-CSC cells. The level of reactive oxygen species after AA treatment was elevated only in CD166- cells. The effect of AA only occurred at low cell densities in 2D and 3D cultures. In a mouse tumor model injected with Li-7 cells, intraperitoneal administration of AA failed to prevent tumor formation but appeared to delay tumor growth. Our findings shed light on why AA administration has not become a mainstream treatment for cancer treatment; however, they also show the possibility that AA can be used in therapies to suppress CSCs. • Effects of ascorbic acid was tested in the hepatocellular carcinoma cell line Li-7. • Ascorbic acid increased the level of reactive oxygen species. • Ascorbic acid caused cell death predominantly in cancer stem cell-like cells. • Effects of AA occurred only at low cell densities in 2D and 3D cultures. • No tumor shrinkage effect of ascorbic acid was observed in a mouse xenograft model. [ABSTRACT FROM AUTHOR]
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- 2024
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5. Gene expression profiles of cryopreserved CD34+ human umbilical cord blood cells are related to their bone marrow reconstitution abilities in mouse xenografts
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Sudo, Kazuhiro, Yasuda, Jun, and Nakamura, Yukio
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BLOOD cells , *CORD blood , *GENE expression , *BONE marrow , *LABORATORY mice , *XENOGRAFTS , *HEMATOPOIETIC stem cells , *CELL transplantation - Abstract
Abstract: Human umbilical cord blood (UCB) cells are an alternative source of hematopoietic stem cells for treatment of leukemia and other diseases. It is very difficult to assess the quality of UCB cells in the clinical situation. Here, we sought to assess the quality of UCB cells by transplantation to immunodeficient mice. Cryopreserved CD34+ UCB cells from twelve different human donors were transplanted into sublethally irradiated NOD/shi-scid Jic mice. In parallel, the gene expression profiles of the UCB cells were determined from oligonucleotide microarrays. UCB cells from three donors failed to establish an engraftment in the host mice, while the other nine succeeded to various extents. Gene expression profiling indicated that 71 genes, including HOXB4, C/EBP-β, and ETS2, were specifically overexpressed and 23 genes were suppressed more than 2-fold in the successful UCB cells compared to those that failed. Functional annotation revealed that cell growth and cell cycle regulators were more abundant in the successful UCB cells. Our results suggest that hematopoietic ability may vary among cryopreserved UCB cells and that this ability can be distinguished by profiling expression of certain sets of genes. [Copyright &y& Elsevier]
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- 2010
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6. Long noncoding RNA HBBP1 enhances γ-globin expression through the ETS transcription factor ELK1.
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Ma, Shuang-Ping, Xi, Hai-Rui, Gao, Xu-Xia, Yang, Jing-Min, Kurita, Ryo, Nakamura, Yukio, Song, Xian-Min, Chen, Hong-Yan, and Lu, Da-Ru
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FETAL hemoglobin , *LINCRNA , *TRANSCRIPTION factors , *GLOBIN genes , *MESSENGER RNA , *PROGENITOR cells , *HEMOGLOBINS - Abstract
β-Thalassemia is an autosomal recessive genetic disease caused by defects in the production of adult hemoglobin (HbA, α 2 β 2), which leads to an imbalance between α- and non-α-globin chains. Reactivation of γ-globin expression is an effective strategy to treat β-thalassemia patients. Previously, it was demonstrated that hemoglobin subunit beta pseudogene 1 (HBBP1) is associated with elevated fetal hemoglobin (HbF, α 2 γ 2) in β-thalassemia patients. However, the mechanism underlying HBBP1 -mediated HbF production is unknown. In this study, using bioinformatics analysis, we found that HBBP1 is involved in γ-globin production, and then preliminarily confirmed this finding in K562 cells. When HBBP1 was overexpressed, γ-globin expression was increased at the transcript and protein levels in HUDEP-2 cells. Next, we found that ETS transcription factor ELK1 (ELK1) binds to the HBBP1 proximal promoter and significantly promotes its activity. Moreover, the synthesis of γ-globin was enhanced when ELK1 was overexpressed in HUDEP-2 cells. Surprisingly, ELK1 also directly bound to and activated the γ-globin proximal promoter. Furthermore, we found that HBBP1 and ELK1 can interact with each other in HUDEP-2 cells. Collectively, these findings suggest that HBBP1 can induce γ-globin by enhancing ELK1 expression, providing some clues for γ-globin reactivation in β-thalassemia. • HBBP1 is related to elevated γ-globin and promotes γ-globin expression by activating ELK1 in HUDEP-2 cells. • HBBP1 interacts with ELK1 and ELK1 directly binds to the proximal promoter of γ-globin in HUDEP-2 cells. • HBBP1-ablation significantly impairs erythroid differentiation in hematopoietic stem/progenitor cell. [ABSTRACT FROM AUTHOR]
- Published
- 2021
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7. Recombinant Cas9 protein production in an endotoxin-free system and evaluation with editing the BCL11A gene in human cells.
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Singpant, Passanan, Tubsuwan, Alisa, Sakdee, Somsri, Ketterman, Albert J., Jearawiriyapaisarn, Natee, Kurita, Ryo, Nakamura, Yukio, Songdej, Duantida, Tangprasittipap, Amornrat, Bhukhai, Kanit, Chiangjong, Wararat, Hongeng, Suradej, and Saisawang, Chonticha
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PROTEIN expression , *ENDOTOXINS , *RECOMBINANT proteins , *GENOME editing , *HUMAN genes , *BACTERIAL proteins - Abstract
Many therapeutic proteins are expressed in Escherichia coli bacteria for the low cost and high yield obtained. However, these gram-negative bacteria also generate undesirable endotoxin byproducts such as lipopolysaccharides (LPS). These endotoxins can induce a human immune response and cause severe inflammation. To mitigate this problem, we have employed the ClearColi BL21 (DE3) endotoxin-free cells as an expression host for Cas9 protein production. Cas9 is an endonuclease enzyme that plays a key role in the C lustered R egularly I nterspaced S hort P alindromic R epeats (CRISPR) and CRISPR associated protein 9 (CRISPR/Cas9) genome editing technique. This technology is very promising for use in diagnostics as well as treatment of diseases, especially for genetic diseases such as thalassemia. The potential uses for this technology thus generate a considerable interest for Cas9 utilization as a therapeutic protein in clinical treatment. Therefore, special care in protein production should be a major concern. Accordingly, we expressed the Cas9 protein in endotoxin-free bacterial cells achieving 99% purity with activity comparable to commercially available Cas9. Our protocol therefore yields a cost-effective product suitable for in vitro experiments with stem cells. • The use of bacterial endotoxin-free cell is one of a good choice for therapeutic protein production. • Purified Cas9 protein expressed in endotoxin-free cells showed no endotoxin contamination. • The purified Cas9 protein was found to be very suitable for in vivo eukaryotic cell experiments. • Our in-house produced Cas9 performed very competitively in comparison to commercial Cas9 protein. [ABSTRACT FROM AUTHOR]
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- 2023
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8. Olfactomedin-like protein OLFML1 inhibits Hippo signaling and mineralization in osteoblasts.
- Author
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Murakami, Kohei, Kikugawa, Shingo, Kobayashi, Yasuhiro, Uehara, Shunsuke, Suzuki, Takako, Kato, Hiroyuki, Udagawa, Nobuyuki, and Nakamura, Yukio
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OLFACTOMEDIN , *OSTEOBLASTS , *MESSENGER RNA , *SCOLIOSIS , *CYTOPLASM - Abstract
Abstract Congenital scoliosis is a lateral curvature of the spine that is due to the presence of vertebral anomalies. Although genetic and environmental factors are involved in the pathogenesis of congenital scoliosis, the specific cause of only a small number of individuals has been identified to date. We identified a de novo missense mutation in the olfactomedin-like 1 (OLFML1) gene by whole-exome sequencing of a patient with congenital scoliosis. Then, we carried out further functional investigation in mice. An assessment of the tissue distribution of Olfml1 revealed it to be prominently expressed in developing skeletal tissues, specifically osteoblasts. Short hairpin RNA-mediated knockdown of Olfml1 in osteoblasts induced the translocation of Yes-associated protein (YAP) transcriptional coactivator from the cytoplasm to the nucleus, which accelerated the Hippo signaling pathway to promote osteoblast mineralization. In contrast, experimentally induced gain of function of Olfml1 retained YAP in the cytoplasm. There appears to exist a novel cell-autonomous mechanism by which osteoblasts avoid excess mineralization through Olfml1. Our results also indicate that mutation of OLFML1 leads to impaired osteoblast differentiation and abnormal development of bone tissue. Graphical abstract Image 1 Highlights • A de novo mutation was identified in OLFML1 in a patient with congenital scoliosis. • Olfml1 is strongly expressed in calvarial osteoblasts in mice. • Knockdown of Olfml1 accelerates osteoblast mineralization. • Olfml1 knockdown induces nuclear translocation of YAP and activates Hippo signaling. • Olfml1 expression vector transfection retains YAP in the cytoplasm. [ABSTRACT FROM AUTHOR]
- Published
- 2018
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9. A long noncoding RNA from the HBS1L-MYB intergenic region on chr6q23 regulates human fetal hemoglobin expression.
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Morrison, Tasha A., Wilcox, Ibifiri, Luo, Hong-Yuan, Farrell, John J., Kurita, Ryo, Nakamura, Yukio, Murphy, George J., Cui, Shuaiying, Steinberg, Martin H., and Chui, David H.k.
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NON-coding RNA , *FETAL hemoglobin , *CELL proliferation , *PROMOTERS (Genetics) , *TRANSCRIPTION factors - Abstract
The HBS1L-MYB intergenic region (chr6q23) regulates erythroid cell proliferation, maturation, and fetal hemoglobin (HbF) expression. An enhancer element within this locus, highlighted by a 3-bp deletion polymorphism (rs66650371), is known to interact with the promoter of the neighboring gene, MYB , to increase its expression, thereby regulating HbF production. RNA polymerase II binding and a 50-bp transcript from this enhancer region reported in ENCODE datasets suggested the presence of a long noncoding RNA (lncRNA). We characterized a novel 1283 bp transcript ( HMI-LNCRNA; chr6:135,096,362–135,097,644; hg38) that was transcribed from the enhancer region of MYB . Within erythroid cells, HMI-LNCRNA was almost exclusively present in nucleus, and was much less abundant than the mRNA for MYB . HMI-LNCRNA expression was significantly higher in erythroblasts derived from cultured adult peripheral blood CD34 + cells which expressed more HBB , compared to erythroblasts from cultured cord blood CD34 + cells which expressed much more HBG . Down-regulation of HMI-LNCRNA in HUDEP-2 cells, which expressed mostly HBB , significantly upregulated HBG expression both at the mRNA (200-fold) and protein levels, and promoted erythroid maturation. No change was found in the expression of BCL11A and other key transcription factors known to modulate HBG expression. HMI-LNCRNA plays an important role in regulating HBG expression, and its downregulation can result in a significant increase in HbF. HMI-LNCRNA might be a potential therapeutic target for HbF induction treatment in sickle cell disease and β-thalassemia. [ABSTRACT FROM AUTHOR]
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- 2018
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10. Effect of 5-aminolevulinic acid on erythropoiesis: A preclinical in vitro characterization for the treatment of congenital sideroblastic anemia.
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Fujiwara, Tohru, Okamoto, Koji, Niikuni, Ryoyu, Takahashi, Kiwamu, Okitsu, Yoko, Fukuhara, Noriko, Onishi, Yasushi, Ishizawa, Kenichi, Ichinohasama, Ryo, Nakamura, Yukio, Nakajima, Motowo, Tanaka, Tohru, and Harigae, Hideo
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ANEMIA treatment , *AMINOLEVULINIC acid , *ERYTHROPOIESIS , *CONGENITAL disorders , *TREATMENT effectiveness - Abstract
Congenital sideroblastic anemia (CSA) is a hereditary disorder characterized by microcytic anemia and bone marrow sideroblasts. The most common form of CSA is attributed to mutations in the X-linked gene 5-aminolevulinic acid synthase 2 ( ALAS2 ). ALAS2 is a mitochondrial enzyme, which utilizes glycine and succinyl-CoA to form 5-aminolevulinic acid (ALA), a crucial precursor in heme synthesis. Therefore, ALA supplementation could be an effective therapeutic strategy to restore heme synthesis in CSA caused by ALAS2 defects. In a preclinical study, we examined the effects of ALA in human erythroid cells, including K562 cells and human induced pluripotent stem cell-derived erythroid progenitor (HiDEP) cells. ALA treatment resulted in significant dose-dependent accumulation of heme in the K562 cell line. Concomitantly, the treatment substantially induced erythroid differentiation as assessed using benzidine staining. Quantitative reverse transcription polymerase chain reaction (RT-PCR) analysis confirmed significant upregulation of heme-regulated genes, such as the globin genes [hemoglobin alpha ( HBA ) and hemoglobin gamma ( HBG )] and the heme oxygenase 1 ( HMOX1 ) gene, in K562 cells. Next, to investigate the mechanism by which ALA is transported into erythroid cells, quantitative RT-PCR analysis was performed on previously identified ALA transporters, including solute carrier family 15 (oligopeptide transporter) , member (SLC15A) 1 , SLC15A2 , solute carrier family 36 (proton/amino acid symporter) , member (SLC36A1) , and solute carrier family 6 (neurotransmitter transporter) , member 13 (SLC6A13) . Our analysis revealed that SLC36A1 was abundantly expressed in erythroid cells. Thus, gamma-aminobutyric acid (GABA) was added to K562 cells to competitively inhibit SLC36A1-mediated transport. GABA treatment significantly impeded the ALA-mediated increase in the number of hemoglobinized cells as well as the induction of HBG , HBA , and HMOX1 . Finally, small-interfering RNA-mediated knockdown of ALAS2 in HiDEP cells considerably decreased the expression of HBA , HBG , and HMOX1 , and these expression levels were rescued with ALA treatment. In summary, ALA appears to be transported into erythroid cells mainly by SLC36A1 and is utilized to generate heme. ALA may represent a novel therapeutic option for CSA treatment, particularly for cases harboring ALAS2 mutations. [ABSTRACT FROM AUTHOR]
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- 2014
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11. Development of enzyme-linked immunosorbent assays for two forms of vitellogenin in Japanese common goby (Acanthogobius flavimanus)
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Ohkubo, Nobuyuki, Mochida, Kazuhiko, Adachi, Shinji, Hara, Akihiko, Hotta, Komei, Nakamura, Yukio, and Matsubara, Takahiro
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ENZYMES , *IMMUNE serums - Abstract
Two vitellogenins (Vgs) were detected in serum from estradiol-17β (
E2 )-injected Japanese common goby (Acanthogobius flavimanus). Vitellogenins with molecular masses of 530 kDa (Vg-530) and 320 kDa (Vg-320) were purified, and used to raise specific antisera in rabbits. Sandwich enzyme-linked immunosorbent assays (ELISAs) for Vg-530 and Vg-320 were developed using the antisera and the isolated Vgs. The sensitivity ranges of these ELISAs were 1.25–160 ng/ml for Vg-530 and 0.26–66 ng/ml for Vg-320, and very low cross-reactivity was found with the alternate Vg in each assay. Treatment of male gobys withE2 by injection and immersion induced both Vgs in sera in a dose-dependent manner. The mean concentrations of the Vgs increased from 10 ng/LE2 exposure for three weeks. Serum concentrations of the two Vgs in field-collected maturing females increased in accordance with increment ofE2 level and ovarian development, and the mean concentrations of Vg-530 were higher than those of Vg-320 in maturing female. These results indicate that the sandwich ELISAs for Vg-530 and Vg-320 developed in the present study is useful as an assay system for surveys of estrogenic activity in coastal areas of Japan. [Copyright &y& Elsevier]- Published
- 2003
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