Department of Cellular Physiology, Institute of Nephrology, Niigata University Graduate School of Medical and Dental Sciences, Japan.
Proc Jpn Acad Ser B Phys Biol Sci. 2011;87(3):81-90. doi: 10.2183/pjab.87.81.
In this review, I introduce the strategy developed by our laboratory to explore the mechanisms of renoprotection against progressive glomerulosclerosis leading to renal death. First, I describe the experimental rat model in which disturbances of vascular regeneration and glomerular hemodynamics lead to irreversible glomerulosclerosis. Second, I discuss the possible mechanisms determining the progression of glomerulosclerosis and introduce a new imaging system based on intravital confocal laser scanning microscopy. Third, I provide an in-depth review of the regulatory glomerular hemodynamics at the cellular and molecular levels while focusing on the pivotal role of Ca(2+)-dependent gap junctional intercellular communication in coordinating the behavior of mesangial cells. Last, I show that local delivery of renoprotective agents, in combination with diagnostic imaging of the renal microvasculature, allows the evaluation of the therapeutic effects of angiotensin II receptor and cyclooxygenase activity local blockade on the progression of glomerulosclerosis, which would otherwise lead to renal death.
在这篇综述中,我介绍了我们实验室开发的策略,以探索针对渐进性肾小球硬化导致肾死亡的肾脏保护机制。首先,我描述了导致不可逆肾小球硬化的血管再生和肾小球血液动力学紊乱的实验性大鼠模型。其次,我讨论了决定肾小球硬化进展的可能机制,并介绍了一种基于活体共聚焦激光扫描显微镜的新成像系统。第三,我深入回顾了细胞和分子水平上调节性肾小球血液动力学,重点关注钙依赖性缝隙连接细胞间通讯在协调系膜细胞行为中的关键作用。最后,我表明,局部递送肾脏保护剂结合肾脏微血管的诊断性成像,可以评估血管紧张素 II 受体和环氧化酶活性局部阻断对肾小球硬化进展的治疗效果,否则会导致肾死亡。