SFB 1350: Tubulussystem und Interstitium der Niere: (Patho-)Physiologie und Crosstalk
SFB 1350:肾小管系统和肾间质:(病理)生理学和串扰
基本信息
- 批准号:387509280
- 负责人:
- 金额:--
- 依托单位:
- 依托单位国家:德国
- 项目类别:Collaborative Research Centres
- 财政年份:2019
- 资助国家:德国
- 起止时间:2018-12-31 至 2021-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Chronic kidney disease (CKD) is of great medical and socio-economic significance and is associated with high mortality. CKD can result from either systemic diseases, such as diabetes mellitus and arterial hypertension, or diseases primarily affecting the kidney, such as primary glomerular diseases, tubular defects, and cystic kidney disease. Regardless of the underlying cause of CKD, the tubular system and interstitial cells are critically involved in either the development or progression of chronic kidney disease and thus have a central position in the pathogenesis of this common disease. Normally, the different cell types of the tubular system and interstitium work together in a coordinated and finely tuned way, thereby allowing the kidney to adapt to various physiological needs. Importantly, many renal disease processes also affect more than one cell type and elicit complex responses in tubules and interstitium. These processes can turn maladaptive and aggravate disease progression. The underlying mechanisms are yet poorly understood and examining the exact nature of the complex crosstalk between tubular cells and interstitial cells is technically demanding and requires an integrative, multidisciplinary approach. The overarching aim of CRC 1350 is to gain insights into the (patho-) physiology of the tubular system and the renal interstitium using a comprehensive and interdisciplinary strategy. In particular, we aim to improve understanding of the diverse functions of the various cell types and their crosstalk during disease progression and regeneration processes in the kidney. The expected results of the collaboration between basic researchers and clinical scientists can help identify novel targets and develop future therapeutic strategies for chronic kidney disease.
慢性肾脏病(CKD)具有重要的医学和社会经济意义,并与高死亡率相关。CKD可由全身性疾病(如糖尿病和动脉高血压)或主要影响肾脏的疾病(如原发性肾小球疾病、肾小管缺陷和囊性肾病)引起。无论CKD的根本原因是什么,肾小管系统和间质细胞都与慢性肾脏疾病的发生或进展密切相关,因此在这种常见疾病的发病机制中具有中心地位。正常情况下,肾小管系统和肾小管的不同细胞类型以协调和微调的方式共同工作,从而使肾脏适应各种生理需求。重要的是,许多肾脏疾病过程也会影响一种以上的细胞类型,并在肾小管和肾小管中引起复杂的反应。这些过程可能导致适应不良并加剧疾病进展。潜在的机制还知之甚少,检查肾小管细胞和间质细胞之间的复杂串扰的确切性质在技术上要求很高,需要综合的多学科方法。 CRC 1350的首要目标是使用全面和跨学科的策略深入了解肾小管系统和肾动脉的(病理)生理学。特别是,我们的目标是提高对各种细胞类型的不同功能及其在肾脏疾病进展和再生过程中的相互作用的理解。基础研究人员和临床科学家之间合作的预期结果可以帮助确定新的靶点,并为慢性肾脏疾病制定未来的治疗策略。
项目成果
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其他文献
吉治仁志 他: "トランスジェニックマウスによるTIMP-1の線維化促進機序"最新医学. 55. 1781-1787 (2000)
Hitoshi Yoshiji 等:“转基因小鼠中 TIMP-1 的促纤维化机制”现代医学 55. 1781-1787 (2000)。
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LiDAR Implementations for Autonomous Vehicle Applications
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2021 - 期刊:
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吉治仁志 他: "イラスト医学&サイエンスシリーズ血管の分子医学"羊土社(渋谷正史編). 125 (2000)
Hitoshi Yoshiji 等人:“血管医学与科学系列分子医学图解”Yodosha(涉谷正志编辑)125(2000)。
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Effect of manidipine hydrochloride,a calcium antagonist,on isoproterenol-induced left ventricular hypertrophy: "Yoshiyama,M.,Takeuchi,K.,Kim,S.,Hanatani,A.,Omura,T.,Toda,I.,Akioka,K.,Teragaki,M.,Iwao,H.and Yoshikawa,J." Jpn Circ J. 62(1). 47-52 (1998)
钙拮抗剂盐酸马尼地平对异丙肾上腺素引起的左心室肥厚的影响:“Yoshiyama,M.,Takeuchi,K.,Kim,S.,Hanatani,A.,Omura,T.,Toda,I.,Akioka,
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