Department of Urology, University of California San Francisco, San Francisco, CA 94143, United States.
Division of Biomaterials and Bioengineering, Department of Preventive and Restorative Dental Sciences, University of California San Francisco, San Francisco, CA 94143, United States.
Acta Biomater. 2018 Apr 15;71:72-85. doi: 10.1016/j.actbio.2018.01.040. Epub 2018 Feb 9.
The development of new modalities for kidney stone prevention rests upon understanding the progression of mineralization within the renal pyramid. The progression from small foci of mineralized volumes within the renal pyramid to larger interstitial plaques that ultimately lead into clinically detectable calcium-based stones on calcium phosphate stems will be presented through correlative microscopy approach. High resolution X-ray computed tomography (micro-XCT), electron microscopy, and energy dispersive X-ray (EDX) compositional analyses of interstitial plaques, stems, and attached stones were performed. Increase in mineral density progressed with mineralization severity, with the highest mineral densities detected within mature Randall's plaque and stems to which kidney stones were attached. EDX analyses revealed variable elemental composition within interstitial plaque, stems, and stones. Micro-XCT reconstructions of stones with stems enabled visualization of unoccluded tubules within stems, with average tubule diameters corresponding to thin limbs of Henle, blood vessels, and collecting ducts. Correlative microscopy confirmed that the progression of mineralization leading to calcium-based nephrolithiasis occurs through a continuum involving four anatomically and structurally distinct biomineralization regions: 1) proximal intratubular mineralization within the renal pyramid; 2) interstitial Randall's plaque near the tip of the papilla; 3) emerging plaque (stems); and, 4) the body of heterogeneous stones.
Nephrolithiasis is a common condition affecting nearly 1 in 11 Americans. The most common type of stone, calcium oxalate is known to form on a calcium phosphate deposit on the renal papilla known as Randall's plaque. Novel imaging techniques have identified distinct regions of biomineralization not just at the tip, but throughout the renal papilla. The classic understanding of Randall's plaque formation is reformulated using correlative imaging techniques. This study establishes a stepwise progression of anatomically-specific biomineralization events including, 1) proximal intratubular mineralization within the renal pyramid; 2) interstitial Randall's plaque near the tip of the papilla; 3) emerging plaque (stems); and, 4) the body of heterogeneous stones, and provides insights into the need for plausible site-specific therapeutic intervention.
肾结石预防的新方法的发展依赖于对肾锥体中矿化进程的理解。本文将通过相关显微镜方法介绍肾锥体中矿物质体积的小焦点进展为更大的间质斑块,最终导致磷酸钙上临床上可检测到的基于钙的结石。对间质斑块、茎和附着结石进行了高分辨率 X 射线计算机断层扫描(微 XCT)、电子显微镜和能量色散 X 射线(EDX)成分分析。矿物质密度的增加与矿化严重程度相关,在成熟的 Randall 斑块和附着结石的茎中检测到最高的矿物质密度。EDX 分析显示间质斑块、茎和结石的元素组成存在差异。带茎的结石的微 XCT 重建使我们能够观察到茎内未堵塞的小管,平均小管直径与 Henle 的薄肢、血管和收集管相对应。相关显微镜证实,导致基于钙的肾结石形成的矿化进展是通过涉及四个解剖学和结构上不同的生物矿化区域的连续过程发生的:1)肾锥体内部管状矿化;2)乳头尖端附近的间质 Randall 斑块;3)新兴斑块(茎);4)异质结石的主体。
肾结石是一种常见疾病,影响近 11 分之一的美国人。最常见的结石类型草酸钙已知在肾乳头的磷酸钙沉积物上形成,称为 Randall 斑块。新型成像技术不仅在尖端,而且在整个肾乳头都确定了不同的生物矿化区域。使用相关成像技术对 Randall 斑块形成的经典理解进行了重新制定。本研究建立了一个逐步的解剖特异性生物矿化事件的进展,包括 1)肾锥体内部管状矿化;2)乳头尖端附近的间质 Randall 斑块;3)新兴斑块(茎);4)异质结石的主体,并深入了解需要合理的特定部位治疗干预的必要性。