Laboratoire de Physique des Solides, CNRS UMR 8502 , Université de Paris-Saclay , F-91405 , Orsay , France.
Sorbonne Université , UPMC Univ Paris 06, UMR S 1155, F-75020 , Paris , France.
ACS Nano. 2020 Feb 25;14(2):1823-1836. doi: 10.1021/acsnano.9b07664. Epub 2020 Jan 27.
Idiopathic kidney stones originate mainly from calcium phosphate deposits at the tip of renal papillae, known as Randall's plaques (RPs), also detected in most human kidneys without stones. However, little is known about the mechanisms involved in RP formation. The localization and characterization of such nanosized objects in the kidney remain a real challenge, making their study arduous. This study provides a nanoscale analysis of the chemical composition and morphology of incipient RPs, characterizing in particular the interface between the mineral and the surrounding organic compounds. Relying on data gathered from a calculi collection, the morphology and chemical composition of incipient calcifications in renal tissue were determined using spatially resolved electron energy-loss spectroscopy. We detected microcalcifications and individual nanocalcifications found at some distance from the larger ones. Strikingly, concerning the smaller ones, we show that two types of nanocalcifications coexist: calcified organic vesicles and nanometric mineral granules mainly composed of calcium phosphate with carbonate in their core. Interestingly, some of these nanocalcifications present similarities with those reported in physiological bone or pathological cardiovascular biominerals, suggesting possible common formation mechanisms. However, the high diversity of these nanocalcifications suggests that several mechanisms may be involved (nucleation on a carbonate core or on organic compounds). In addition, incipient RPs also appear to present specific features at larger scales, revealing secondary calcified structures embedded in a fibrillar organic material. Our study proves that analogies exist between physiological and pathological biominerals and provides information to understand the physicochemical processes involved in pathological calcification formation.
特发性肾结石主要源于肾乳头尖端的磷酸钙沉积物,称为 Randall 斑块(RPs),在大多数无结石的人类肾脏中也能检测到。然而,关于 RPs 形成的机制知之甚少。这些纳米级物体在肾脏中的定位和特征仍然是一个真正的挑战,使得它们的研究变得艰巨。本研究对初发 RPs 的化学组成和形态进行了纳米尺度分析,特别是对矿物质与周围有机化合物的界面进行了特征描述。本研究基于结石收集的数据,使用空间分辨电子能量损失光谱法确定了肾组织中初发钙化的形态和化学成分。我们检测到了微钙化和一些远离较大钙化的单个纳米钙化。值得注意的是,对于较小的钙化,我们发现存在两种类型的纳米钙化:钙化有机囊泡和纳米级矿物颗粒,主要由磷酸钙组成,其核心有碳酸盐。有趣的是,其中一些纳米钙化与生理骨或病理心血管生物矿物质中报道的相似,表明可能存在共同的形成机制。然而,这些纳米钙化的多样性表明可能涉及几种机制(在碳酸盐核心或有机化合物上成核)。此外,初发 RPs 在较大尺度上也呈现出特定的特征,揭示了嵌入纤维状有机材料中的次级钙化结构。我们的研究证明了生理和病理生物矿物质之间存在相似性,并提供了信息来理解病理钙化形成涉及的物理化学过程。