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Article ; Online: The expression of trefoil factor family member 2 in increased at an acidic pH.

Masumoto, Yui / Matsuo, Suzuka / Kinjou, Natsuno / Narieda, Yuka / Wada, Morimasa / Fujimoto, Kyoko

2024 Volume 27, Issue 5, Page(s) 212

Abstract: Trefoil factor family member 2 ( ...

Abstract	Trefoil factor family member 2 (
Language	English
Publishing date	2024-03-15
Publishing country	Greece
Document type	Journal Article
ZDB-ID	2573196-8
ISSN	1792-1082 ; 1792-1074
ISSN (online)	1792-1082
ISSN	1792-1074
DOI	10.3892/ol.2024.14345
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Article ; Online: A rare case of metastatic extramammary Paget disease developing transfusion-related acute lung injury during chemotherapy.

Kurokami, Yu / Yamashita, Chigusa / Yokoi, Kazunori / Tonomura, Kyoko / Ishitsuka, Yosuke / Yoshida, Takeshi / Koyama, Yukiko / Fujino, Yuji / Fujimoto, Manabu / Tanemura, Atsushi

The Journal of dermatology

2024

Language	English
Publishing date	2024-04-11
Publishing country	England
Document type	Letter
ZDB-ID	800103-0
ISSN	1346-8138 ; 0385-2407
ISSN (online)	1346-8138
ISSN	0385-2407
DOI	10.1111/1346-8138.17223
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Article ; Online: Leukemia inhibitory factor shortens primary cilia by upregulating C-C motif chemokine 2 in human neural stem/progenitor cells.

Takahashi, Hisashi / Fujimoto, Takahiro / Yaoi, Takeshi / Fushiki, Shinji / Itoh, Kyoko

Genes to cells : devoted to molecular & cellular mechanisms

2023 Volume 28, Issue 12, Page(s) 868–880

Abstract: Primary cilia on neural stem/progenitor cells (NSPCs) play an important role in determining cell fate, although the regulatory mechanisms involved in the ciliogenesis remain largely unknown. In this study, we analyzed the effect of the leukemia ... ...

Abstract	Primary cilia on neural stem/progenitor cells (NSPCs) play an important role in determining cell fate, although the regulatory mechanisms involved in the ciliogenesis remain largely unknown. In this study, we analyzed the effect of the leukemia inhibitory factor (LIF) for the primary cilia in immortalized human NSPCs. LIF withdrawal elongated the primary cilia length, whereas the addition of LIF shortened it. Microarray gene expression analysis revealed that differentially expressed genes (DEGs) associated with LIF treatment were related with the multiple cytokine signaling pathways. Among the DEGs, C-C motif chemokine 2 (CCL2) had the highest ranking and its increase in the protein concentration in the NSPCs-conditioned medium after the LIF treatment was confirmed by ELISA. Interestingly, we found that CCL2 was a negative regulator of cilium length, and LIF-induced shortening of primary cilia was antagonized by CCL2-specific antibody, suggesting that LIF could influence cilia length via upregulating CCL2. The shortening effect of LIF and CCL2 on primary cilia was also observed in SH-SY5Y cells. The results of the study suggested that the LIF-CCL2 axis may well be a regulator of NSPCs and its primary cilia length, which could affect multiple cellular processes, including NSPC proliferation and differentiation.
MeSH term(s)	Humans ; Cilia/metabolism ; Signal Transduction ; Leukemia Inhibitory Factor/genetics ; Leukemia Inhibitory Factor/metabolism ; Leukemia Inhibitory Factor/pharmacology ; Neuroblastoma ; Neural Stem Cells/metabolism ; Cell Differentiation/physiology
Chemical Substances	Leukemia Inhibitory Factor
Language	English
Publishing date	2023-10-14
Publishing country	England
Document type	Journal Article
ZDB-ID	1330000-3
ISSN	1365-2443 ; 1356-9597
ISSN (online)	1365-2443
ISSN	1356-9597
DOI	10.1111/gtc.13074
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Zs.A 4539: Show issues

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Article: Low Doses of Bisphenol A Disrupt Neuronal Differentiation of Human Neuronal Stem/Progenitor Cells.

Kiso-Farnè, Kaori / Yaoi, Takeshi / Fujimoto, Takahiro / Itoh, Kyoko

Acta histochemica et cytochemica

2022 Volume 55, Issue 6, Page(s) 193–202

Abstract: Bisphenol A (BPA) is an endocrine disrupting chemical. Human epidemiological studies have suggested that adverse neurobehavioral outcomes are induced by fetal exposure to BPA. The remarkable differences in the corticogenesis between human and ... ...

Abstract	Bisphenol A (BPA) is an endocrine disrupting chemical. Human epidemiological studies have suggested that adverse neurobehavioral outcomes are induced by fetal exposure to BPA. The remarkable differences in the corticogenesis between human and agyrencephalic mammals are an increase in the intermediate progenitor cells (IPCs) and a following increase in the subplate thickness. It is uncertain whether low doses of BPA (low-BPA) affect human early corticogenesis when basal progenitor cells (BPs) produce IPCs resulting in amplified neurogenesis. In this study, human-derived neuronal stem/progenitor cells were exposed to low-BPA or the vehicle only, and the resultant cell type-specific molecular changes and morphology were analyzed. We focused on stem cells immunoreactive for SOX2, BPs for NHLH1, and immature neurons for DCX. SOX2-positive cells significantly decreased at day
Language	English
Publishing date	2022-12-20
Publishing country	Japan
Document type	Journal Article
ZDB-ID	280005-6
ISSN	1347-5800 ; 0044-5991
ISSN (online)	1347-5800
ISSN	0044-5991
DOI	10.1267/ahc.22-00090
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Zs.A 1275: Show issues

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Article ; Online: Myosin Va, a Novel Interaction Partner of STXBP1, Is Required to Transport Syntaxin1A to the Plasma Membrane.

Taura, Yoshihiro / Tozawa, Takenori / Fujimoto, Takahiro / Ichise, Eisuke / Chiyonobu, Tomohiro / Itoh, Kyoko / Iehara, Tomoko

Neuroscience

2023 Volume 524, Page(s) 256–268

Abstract: Syntaxin-binding protein 1 (STXBP1, also known as Munc18-1) regulates exocytosis as a chaperone protein of Syntaxin1A. The haploinsufficiency of STXBP1 causes early infantile-onset developmental and epileptic encephalopathy, known as STXBP1 ... ...

Abstract	Syntaxin-binding protein 1 (STXBP1, also known as Munc18-1) regulates exocytosis as a chaperone protein of Syntaxin1A. The haploinsufficiency of STXBP1 causes early infantile-onset developmental and epileptic encephalopathy, known as STXBP1 encephalopathy. Previously, we reported impaired cellular localization of Syntaxin1A in induced pluripotent stem cell-derived neurons from an STXBP1 encephalopathy patient harboring a nonsense mutation. However, the molecular mechanism of abnormal Syntaxin1A localization in the haploinsufficiency of STXBP1 remains unknown. This study aimed to identify the novel interacting partner of STXBP1 involved in transporting Syntaxin1A to the plasma membrane. Affinity purification coupled with mass spectrometry analysis identified a motor protein Myosin Va as a potential binding partner of STXBP1. Co-immunoprecipitation analysis of the synaptosomal fraction from the mouse and tag-fused recombinant proteins revealed that the STXBP1 short splice variant (STXBP1S) interacted with Myosin Va in addition to Syntaxin1A. These proteins colocalized at the tip of the growth cone and axons in primary cultured hippocampal neurons. Furthermore, RNAi-mediated gene silencing in Neuro2a cells showed that STXBP1 and Myosin Va were required for membrane trafficking of Syntaxin1A. In conclusion, this study proposes a potential role of STXBP1 in the trafficking of the presynaptic protein Syntaxin1A to the plasma membrane in conjunction with Myosin Va.
MeSH term(s)	Animals ; Mice ; Brain Diseases/genetics ; Cell Membrane/metabolism ; Munc18 Proteins/genetics ; Munc18 Proteins/metabolism ; Neurons/metabolism ; RNA Interference
Chemical Substances	Munc18 Proteins ; Stx1a protein, mouse ; Myo5a protein, mouse ; Stxbp1 protein, mouse
Language	English
Publishing date	2023-06-12
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	196739-3
ISSN	1873-7544 ; 0306-4522
ISSN (online)	1873-7544
ISSN	0306-4522
DOI	10.1016/j.neuroscience.2023.05.031
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Zs.A 1215: Show issues

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Article ; Online: Dystrophin Short Product, Dp71, Interacts with AQP4 and Kir4.1 Channels in the Mouse Cerebellar Glial Cells in Contrast to Dp427 at Inhibitory Postsynapses in the Purkinje Neurons.

Fujimoto, Takahiro / Stam, Kirsten / Yaoi, Takeshi / Nakano, Kenta / Arai, Tetsuya / Okamura, Tadashi / Itoh, Kyoko

Molecular neurobiology

2023 Volume 60, Issue 7, Page(s) 3664–3677

Abstract: Dystrophin is the causative gene for Duchenne and Becker muscular dystrophy (DMD/BMD), and it produces full-length and short dystrophin, Dp427 and Dp71, respectively, in the brain. The existence of the different dystrophin molecular complexes has been ... ...

Abstract	Dystrophin is the causative gene for Duchenne and Becker muscular dystrophy (DMD/BMD), and it produces full-length and short dystrophin, Dp427 and Dp71, respectively, in the brain. The existence of the different dystrophin molecular complexes has been known for a quarter century, so it is necessary to derive precise expression profiles of the molecular complexes in the brain to elucidate the mechanism of cognitive symptoms in DMD/BMD patients. In order to investigate the Dp71 expression profile in cerebellum, we employed Dp71-specific tag-insertion mice, which allowed for the specific detection of endogenous Dp71 in the immunohistochemical analysis and found its expressions in the glial cells, Bergmann glial (BG) cells, and astrocytes, whereas Dp427 was exclusively expressed in the inhibitory postsynapses within cerebellar Purkinje cells (PCs). Interestingly, we found different cell-type dependent dystrophin molecular complexes; i.e., glia-associated Dp71 was co-expressed with dystroglycan (DG) and dystrobrevinα, whereas synapse-associated Dp427 was co-expressed with DG and dystrobrevinβ. Furthermore, we investigated the molecular relationship of Dp71 to the AQP4 water channel and the Kir4.1 potassium channel, and found biochemical associations of Dp71 with AQP4 and Kir4.1 in both the cerebellum and cerebrum. Immunohistochemical and cytochemical investigations revealed partial co-localizations of Dp71 with AQP4 and Kir4.1 in the glial cells, indicating Dp71 interactions with the channels in the BG cells and astrocytes. Taken together, different cell-types, glial cells and Purkinje neurons, in the cerebellum express different dystrophin molecular complexes, which may contribute to pathological and physiological processes through the regulation of the water/ion channel and inhibitory postsynapses.
MeSH term(s)	Mice ; Animals ; Dystrophin/metabolism ; Purkinje Cells/metabolism ; Synapses/metabolism ; Cerebellum/metabolism ; Neuroglia/metabolism ; Aquaporins/metabolism ; Potassium Channels, Inwardly Rectifying/metabolism
Chemical Substances	Dystrophin ; Aquaporins ; Potassium Channels, Inwardly Rectifying
Language	English
Publishing date	2023-03-15
Publishing country	United States
Document type	Journal Article
ZDB-ID	645020-9
ISSN	1559-1182 ; 0893-7648
ISSN (online)	1559-1182
ISSN	0893-7648
DOI	10.1007/s12035-023-03296-w
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Zs.A 2411: Show issues

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Article ; Online: Dermatofibrosarcoma protuberans of the cheek without surface alteration.

Kaneda, Emi / Yamashita, Chigusa / Tonomura, Kyoko / Kiyohara, Eiji / Ishitsuka, Yosuke / Arase, Noriko / Seike, Shien / Kubo, Tateki / Fujimoto, Manabu / Tanemura, Atsushi

European journal of dermatology : EJD

2023 Volume 33, Issue 3, Page(s) 306–307

MeSH term(s)	Humans ; Cheek ; Dermatofibrosarcoma/surgery ; Skin Neoplasms/surgery
Language	English
Publishing date	2023-08-18
Publishing country	France
Document type	Journal Article
ZDB-ID	1128666-0
ISSN	1952-4013 ; 1167-1122
ISSN (online)	1952-4013
ISSN	1167-1122
DOI	10.1684/ejd.2023.4457
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Zs.A 3484: Show issues

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Article ; Online: Electric Field Comparison for TMS Using Different Neuroimaging Segmentation Methods.

Zaidi, Tayeb A / Makarov, Sergey N / Fujimoto, Kyoko

Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference

2021 Volume 2021, Page(s) 6565–6568

Abstract: Computational electromagnetic modeling is a powerful technique to evaluate the effects of electrical stimulation of the human brain. The results of these simulations can vary depending on the specific segmentation of the head and brain generated from the ...

Abstract	Computational electromagnetic modeling is a powerful technique to evaluate the effects of electrical stimulation of the human brain. The results of these simulations can vary depending on the specific segmentation of the head and brain generated from the patient images. Using an existing boundary element fast multipole method (BEM-FMM) electromagnetic solver, this work evaluates the electric field differences modeled using two neuroimaging segmentation methods. A transcranial magnetic stimulation (TMS) coil targeting both the primary motor cortex and the dorsolateral prefrontal cortex (DLPFC) was simulated. Average field differences along a 100 mm line from the coil were small (2% for motor cortex, 3% for DLPFC) and the average field differences in the regions directly surrounding the target stimulation point were 5% for the motor cortex and 2% for DLPFC. More studies evaluating different coils and other segmentation options may further improve the computational modeling for robust TMS treatment.Clinical relevance- Patient-specific computational modeling will provide more information to clinicians for improved localization and targeting of neuromodulation therapies.
MeSH term(s)	Brain/diagnostic imaging ; Dorsolateral Prefrontal Cortex ; Humans ; Motor Cortex/diagnostic imaging ; Neuroimaging ; Transcranial Magnetic Stimulation
Language	English
Publishing date	2021-12-10
Publishing country	United States
Document type	Journal Article
ISSN	2694-0604
ISSN (online)	2694-0604
DOI	10.1109/EMBC46164.2021.9630719
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Article ; Online: Evaluation of antimicrobial use in dairy cattle, beef cattle and broilers in Japan using dosage-based indicators.

Abe, Reiko / Fujimoto, Kyoko / Endo, Yuko / Sugiura, Katsuaki

The Journal of veterinary medical science

2021 Volume 83, Issue 12, Page(s) 1826–1837

Abstract: The sales amount of antimicrobials intended for use in dairy cattle, beef cattle and broilers from 2008 to 2019 was evaluated for each antimicrobial class and administration route using dosage-based indicators. Our results revealed that the antimicrobial ...

Abstract	The sales amount of antimicrobials intended for use in dairy cattle, beef cattle and broilers from 2008 to 2019 was evaluated for each antimicrobial class and administration route using dosage-based indicators. Our results revealed that the antimicrobial sales amount sold for use in dairy cattle in 2019 in terms of total weight of active ingredient, the number of defined daily doses (DDDs) (theoretical amount of biomass subjected to antimicrobial treatment in a year) and the number of treatment days (TDs) (theoretical number of days of treatment that an animal is subjected to in a year) calculated using Japanese DDD values (DDDjp values) was 36,751 kg, 8,261,848,000 kg·days and 15.5 days, respectively. Likewise, the antimicrobial sales amount sold for use in beef cattle and broilers in 2019 in terms of these metrics was 33,403 kg, 3,928,248,000 kg·days and 3.61 days, and 69,773 kg, 2,947,848,000 kg·days and 10.66 days, respectively. There was a considerable difference between the number of DDDs calculated using DDDjp values and that calculated using European DDD values (DDDvet values) for antimicrobial products sold for use in dairy and beef cattle. Our results also revealed that the sales amount of some antimicrobials, such as cephalosporins and quinolones represented larger proportions when calculated using dosage-based indicators than when calculated using the weight of active ingredient. Considering that Japanese veterinarians and farmers are more likely to conform to the Japanese dosage recommendations rather than the European ones, these results indicate the need for using dosage-based metrics, in particular metrics based on Japanese dosages rather than European dosages.
MeSH term(s)	Animals ; Anti-Bacterial Agents/therapeutic use ; Anti-Infective Agents ; Cattle ; Chickens ; Commerce ; Japan
Chemical Substances	Anti-Bacterial Agents ; Anti-Infective Agents
Language	English
Publishing date	2021-10-08
Publishing country	Japan
Document type	Journal Article
ZDB-ID	1071753-5
ISSN	1347-7439 ; 0916-7250
ISSN (online)	1347-7439
ISSN	0916-7250
DOI	10.1292/jvms.21-0385
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Zs.B 579: Show issues

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Article ; Online: Age distribution and prevalence in different age groups of four myositis-specific autoantibodies, including anti-ARS, anti-MDA5, anti-Mi-2, and anti-TIF1γ antibodies.

Ueda-Hayakawa, Ikuko / Tonomura, Kyoko / Maekawa, Aya / Kaneda, Emi / Arase, Noriko / Fujimoto, Manabu

The Journal of dermatology

2023 Volume 50, Issue 8, Page(s) 1058–1062

Abstract: We accumulated the demographic information and analyzed the prevalence of myositis-specific antibodies (MSAs) in a large cohort across Japan as standard testing for MSAs becomes more widely available. This retrospective, observational, cohort study ... ...

Abstract	We accumulated the demographic information and analyzed the prevalence of myositis-specific antibodies (MSAs) in a large cohort across Japan as standard testing for MSAs becomes more widely available. This retrospective, observational, cohort study analyzed the records of individuals aged 0-99 years who are tested for serum MSAs at SRL Incorporation from January 2014 to April 2020 across Japan. An enzyme-linked immunosorbent assay testing was applied to determine the presence of anti-aminoacyl tRNA synthetase (anti-ARS), anti-Mi-2, anti-melanoma differentiation-associated gene 5 (anti-MDA5), or anti-transcriptional intermediary factor 1-γ (anti-TIF1γ) (Medical and Biological Laboratories). Anti-TIF1γ antibody was detected more in male patients than female patients. In contrast, women were predominant in patients with other MSAs. More than half of the anti-ARS or anti-TIF1γ antibody-positive patients were over 60 years old, although anti-MDA5 or anti-Mi-2-positive patients were mostly under <60 years old. Anti-MDA5 antibody-positive patients were mostly aged 40-59 years, while other MSA groups were mostly 60-79 years. Anti-MDA5 antibody was detected most frequently in the age range of 0-29 years. Anti-TIF1γ antibody was the second most commonly detected autoantibody in the age range of 0-19 years. Anti-ARS antibody was the most frequently detected autoantibody after the age of 30 years, and the frequency of anti-ARS gradually increased at more advanced ages. The second and third most detected autoantibodies were anti-MDA5 and anti-TIF1γ, respectively, in ages 30-79 years. We performed a nationwide >3-year evaluation of MSA detection in a routine diagnostic setting. This paper provides clinical images concerning the relationship between four MSA types and the distribution of sex and age in a large population.
MeSH term(s)	Adolescent ; Adult ; Child ; Child, Preschool ; Female ; Humans ; Infant ; Infant, Newborn ; Male ; Middle Aged ; Young Adult ; Age Distribution ; Amino Acyl-tRNA Synthetases ; Autoantibodies ; Cohort Studies ; Dermatomyositis/diagnosis ; Dermatomyositis/epidemiology ; Myositis/diagnosis ; Myositis/epidemiology ; Prevalence ; Retrospective Studies ; Aged
Chemical Substances	Amino Acyl-tRNA Synthetases (EC 6.1.1.-) ; Autoantibodies ; Mi-2 antibodies
Language	English
Publishing date	2023-03-08
Publishing country	England
Document type	Observational Study ; Journal Article
ZDB-ID	800103-0
ISSN	1346-8138 ; 0385-2407
ISSN (online)	1346-8138
ISSN	0385-2407
DOI	10.1111/1346-8138.16772
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