研究者業績
基本情報
- 所属
- 藤田医科大学 医療科学部 臨床教育連携ユニット 病態システム解析医学分野 医療准教授
- 学位
- 医学博士(山梨大学)医師免許死体解剖資格認定
- J-GLOBAL ID
- 200901046035768325
- researchmap会員ID
- 6000017924
- 外部リンク
経歴
7-
2024年4月 - 現在
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2018年10月 - 2024年3月
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2018年4月 - 2018年10月
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2016年9月 - 2018年3月
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2016年4月 - 2016年8月
学歴
3-
2003年4月 - 2008年3月
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1994年4月 - 2000年3月
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1991年4月 - 1994年3月
委員歴
6-
2020年10月 - 現在
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2014年5月 - 現在
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2021年8月 - 2022年8月
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2018年6月 - 2019年6月
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2018年8月 - 2018年8月
受賞
3論文
61-
Disease models & mechanisms 17(5) 2024年5月1日Diabetic nephropathy (DN), as a complication of diabetes, is a substantial healthcare challenge owing to the high risk of morbidity and mortality involved. Although significant progress has been made in understanding the pathogenesis of DN, more efficient models are required to develop new therapeutics. Here, we created a DN model in zebrafish by crossing diabetic Tg(acta1:dnIGF1R-EGFP) and proteinuria-tracing Tg(l-fabp::VDBP-GFP) lines, named zMIR/VDBP. Overfed adult zMIR/VDBP fish developed severe hyperglycemia and proteinuria, which were not observed in wild-type zebrafish. Renal histopathology revealed human DN-like characteristics, such as glomerular basement membrane thickening, foot process effacement and glomerular sclerosis. Glomerular dysfunction was restored upon calorie restriction. RNA sequencing analysis demonstrated that DN zebrafish kidneys exhibited transcriptional patterns similar to those seen in human DN pathogenesis. Notably, the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt) signaling pathway was activated, a phenomenon observed in the early phase of human DN. In addition, metformin improved hyperglycemia and proteinuria in DN zebrafish by modulating Akt phosphorylation. Our results indicate that zMIR/VDBP fish are suitable for elucidating the mechanisms underlying human DN and could be a powerful tool for therapeutic discovery.
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PloS one 18(2) e0281770 2023年 査読有り筆頭著者責任著者A long-term high-fat diet (HFD) causes obesity and changes in renal lipid metabolism and lysosomal dysfunction in mice, causing renal damage. Sodium-glucose co-transporter inhibitors, including phlorizin, exert nephroprotective effects in patients with chronic kidney disease, but the underlying mechanism remains unclear. A HFD or standard diet was fed to adult C57BL/6J male mice, and phlorizin was administered. Lamellar body components of the proximal tubular epithelial cells (PTECs) were investigated. After phlorizin administration in HFD-fed mice, sphingomyelin and ceramide in urine and tissues were assessed and label-free quantitative proteomics was performed using kidney tissue samples. Mitochondrial elongation by fusion was effective in the PTECs of HFD-fed obese mice under phlorizin administration, and many lamellar bodies were found in the apical portion of the S2 segment of the proximal tubule. Phlorizin functioned as a diuretic, releasing lamellar bodies from the apical membrane of PTECs and clearing the obstruction in nephrons. The main component of the lamellar bodies was sphingomyelin. On the first day of phlorizin administration in HFD-fed obese mice, the diuretic effect was increased, and more sphingomyelin was excreted through urine than in vehicle-treated mice. The expressions of three peroxisomal β-oxidation proteins involved in fatty acid metabolism were downregulated after phlorizin administration in the kidneys of HFD-fed mice. Fatty acid elongation protein levels increased with phlorizin administration, indicating an increase in long-chain fatty acids. Lamellar bodies accumulated in the proximal renal tubule of the S2 segment of the HFD-fed mice, indicating that the urinary excretion of lamellar bodies has nephroprotective effects.
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Acta Neuropathologica Communications 10(172) 172-172 2022年11月 査読有り
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Science Advances 8(44) eabq1081 2022年11月 査読有り
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Scientific Reports 10(12372) 2020年6月23日 査読有り
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Clinical and experimental nephrology 23(6) 773-781 2019年6月 査読有りBACKGROUND: The interaction among the glomerular components plays an important role in the development of glomerular lesions; thus, investigation of the ultrastructural three-dimensional (3D) configuration of the human glomerular cells and extracellular matrix (ECM) is important for understanding the pathogenesis of glomerulosclerosis, especially glomerulonephritis. METHODS: We applied a new technique of serial block-face scanning electron microscopy (SBF-SEM), which helps to acquire serial electron microscopic images to reconstruct a 3D ultrastructure, to a human kidney biopsy specimen obtained from a 25-year-old woman with lupus nephritis. RESULTS: SBF-SEM demonstrated that the cytoplasmic processes of the podocyte penetrated into the lamina densa of the glomerular basement membrane, and was in direct contact with the cytoplasm of mesangial cells at the site of mesangial interposition. CONCLUSION: Although this is a single-case observational study, SBF-SEM revealed a unique 3D configuration, suggesting a novel mechanism of direct intercellular cross-communication between podocytes and mesangial cells, aside from the presumed paracrine communication.
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Biophysical Journal 116(3 Supple1) 572A 2019年2月 査読有り
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日本腎臓学会誌 60(6) 887-887 2018年8月
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Biophysical Journal 114(3) 164a-164a 2018年2月 査読有り
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Acta Histochemica et Cytochemica 51(1) 9-20 2018年 査読有り
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SCIENTIFIC REPORTS 7(1) 4942 2017年7月 査読有り
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CELL DEATH & DISEASE 8(6) e2857 2017年6月 査読有り
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MEDICAL MOLECULAR MORPHOLOGY 49(3) 154-162 2016年9月 査読有り
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SCIENTIFIC REPORTS 6 23721. 2016年3月 査読有り
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MICROSCOPY 64(3) 189-203 2015年6月 査読有り
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MICROSCOPY 64(1) 17-26 2015年2月 査読有り
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In Vivo Cryotechnique in Biomedical Research and Application for Bioimaging of Living Animal Organs 87-92 2015年1月1日 査読有り
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In Vivo Cryotechnique in Biomedical Research and Application for Bioimaging of Living Animal Organs 135-140 2015年1月1日 査読有り
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In Vivo Cryotechnique in Biomedical Research and Application for Bioimaging of Living Animal Organs 33-38 2015年1月1日 査読有り
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In Vivo Cryotechnique in Biomedical Research and Application for Bioimaging of Living Animal Organs 51-56 2015年1月1日 査読有り
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Microscopy and Microanalysis 18(5) 1030-1036 2012年10月 査読有り
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Medical Molecular Morphology 45(3) 129-139 2012年6月 査読有り
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HISTOCHEMISTRY AND CELL BIOLOGY 137(2) 137-151 2012年2月 査読有り
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MOLECULAR AND CELLULAR BIOLOGY 32(1) 199-205 2012年1月 査読有り
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MEDICAL MOLECULAR MORPHOLOGY 44(2) 93-102 2011年6月 査読有り
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NEUROSCIENCE LETTERS 488(2) 193-198 2011年1月 査読有り
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ACTA HISTOCHEMICA ET CYTOCHEMICA 44(2) 61-72 2011年 査読有り
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ACTA HISTOCHEMICA ET CYTOCHEMICA 44(2) 81-90 2011年 査読有り
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MICROVASCULAR RESEARCH 80(3) 491-498 2010年12月 査読有り
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JOURNAL OF IMMUNOLOGICAL METHODS 361(1-2) 64-74 2010年9月 査読有り
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J Electron Microsc (Tokyo). 2010;59(6):513-25. 59(6) 513-525 2010年8月 査読有り
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J Electron Microsc (Tokyo). 59(5) 395-408 2010年6月
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REPRODUCTION 139(5) 883-892 2010年5月 査読有り
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HISTOCHEMISTRY AND CELL BIOLOGY 133(2) 229-239 2010年2月 査読有り
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Methods in Molecular Biology 657 167-179 2010年 査読有り
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JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY 57(9) 883-888 2009年9月 査読有り
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CELL AND TISSUE RESEARCH 337(1) 91-102 2009年7月 査読有り
MISC
38-
日本薬理学会年会要旨集 94 3-O-E2-2 2021年White matter abnormalities have been implicated in psychiatric diseases such as major depressive disorder (MDD) ; however, the underlying mechanisms remain poorly understood. The structure and function of the corpus callosum are particularly vulnerable to stress, which may lead to MDD. In the present study, we investigated whether chronic social defeat stress (CSDS) induces myelin abnormalities of the corpus callosum through inflammation that contributes to the pathogenesis of MDD. To produce CSDS, the adult C57BL/6J mouse was exposed to an aggressor ICR mouse for 10 consecutive days. CSDS decreased mature oligodendrocytes in the corpus callosum, and persistently developed depression-like behaviors such as increased immobility in the forced swimming test and impaired social interaction. On transmission electron microscopy, myelin abnormalities and axonal degeneration were observed with necrosis-like cell death of oligodendrocytes in the corpus callosum. Interestingly, CSDS significantly increased the Gasdermin D (Gsdmd), a marker of pyroptosis, concomitantly with enhanced IL-1β production in the corpus callosum. Administration of IL-1β inhibitor prevented the decrease of oligodendrocytes and CSDS-induced depression-like behaviors. These findings suggest that IL-1β acts as a crucial mediator of oligodendroglial pyroptosis induced by the CSDS, which may be responsible for the development of MDD.
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PEDIATRIC BLOOD & CANCER 64 S96-S97 2017年11月
書籍等出版物
10-
IntechOpen: Electron Microscopy - Novel Microscopy Trends 2018年9月
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In Vivo Cryotechnique in Biomedical Research and Application for Bioimaging of Living Animal Organs 2016年
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In Vivo Cryotechnique in Biomedical Research and Application for Bioimaging of Living Animal Organs 2016年
担当経験のある科目(授業)
5-
統合講義 (臨床解剖学, 人体発生学) (山梨大学 医学部)
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肉眼解剖学 (帝京科学大学)
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人体発生学 (藤田医科大学 医学部)
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組織学 (山梨大学 医学部, 藤田医科大学 医学部, 帝京科学大学)
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神経解剖学 (山梨大学 医学部)
所属学協会
7共同研究・競争的資金等の研究課題
6-
2023年 - 2025年
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日本学術振興会 科学研究費助成事業 基盤研究(C) 2020年4月 - 2023年3月
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科研費 基盤(C) (分担) 2018年4月 - 2020年3月
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科研費 基盤(C) 2016年4月 - 2020年3月
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科研費 若手研究(B) 2013年4月 - 2014年3月