Dardamanis M
Nephrology Department, General Hospital of Preveza, Preveza, Greece.
Hippokratia. 2013 Apr;17(2):100-7.
Lithiasis continues to be an important factor in chronic renal disease, since it leads to chronic tubulo-interstitial nephritis, which is estimated to be involved in 15- 30% of cases of end stage chronic renal insufficiency. It is believed that in order for a stone to be formed, a solid phase needs to be first produced from microcrystals (the nucleus), which are formed from salts (and other substances) that are found dissolved in the urine (nucleosis of crystals). Afterwards, the crystals that constitute the core increase in size and link up with each other (incorporation). The main physiochemical factors that participate in the creation of the nucleus are the hypersaturation of urine, the lack of inhibitors of nucleosis and probably the organic substrate. In order for the increase in size and the incorporation of crystals to take place, hypersaturation, the lack of inhibitors, the organic substrate and the epitaxis, during which crystals of a substance are attached to the surface of other crystals of a different chemical structure (e.g. crystals of oxalic calcium onto crystals of uric acid) are needed. Various molecules have been found in urine, which modify to an important degree the adherence of crystals to the surface of epithelial cells. It also seems very likely that certain reactions of renal epithelial cells that follow the uptake of calcium oxalate monohydrate (COM) crystals are due to oxalate ions, which are released during the process of deconstruction of the intracellular crystals. From here, the crystals migrate in the median tissue, where an inflammatory reaction takes place and finally the crystals are destroyed. Macrophages gather in the crystals of the median tissue. The osteopontin which is related to the crystals acts as a chemotactic factor for the macrophages and therefore is perhaps involved in this process too. The uptake of crystals appears to be subjected to regulating mechanisms, as molecules which regulate the endocytosis of COM crystals, a process that is related to changes in the special components of the cytoskeleton, have been observed. In conclusion, the processes of adherence and of endocytosis promote the detention of crystals in the nephron, whilst intracellular deconstruction is an important factor of defence against the deposition of calcium in the kidney.
结石病仍然是慢性肾病的一个重要因素,因为它会导致慢性肾小管间质性肾炎,据估计,在终末期慢性肾功能不全病例中,有15%至30%与此有关。据信,为了形成结石,首先需要从微晶(核)中产生固相,微晶由溶解在尿液中的盐(和其他物质)形成(晶体成核)。之后,构成核心的晶体尺寸增大并相互连接(聚集)。参与核形成的主要物理化学因素是尿液的过饱和、缺乏晶体成核抑制剂以及可能的有机底物。为了使晶体尺寸增大和聚集发生,需要过饱和、缺乏抑制剂、有机底物和取向附生,在此过程中,一种物质的晶体附着在另一种不同化学结构的晶体表面(例如草酸钙晶体附着在尿酸晶体上)。已在尿液中发现各种分子,它们在很大程度上改变了晶体与上皮细胞表面的粘附。很可能,肾上皮细胞在摄取一水合草酸钙(COM)晶体后发生的某些反应是由于草酸根离子,这些离子在细胞内晶体解构过程中释放。从此处开始,晶体在中间组织中迁移,在那里发生炎症反应,最终晶体被破坏。巨噬细胞聚集在中间组织的晶体中。与晶体相关的骨桥蛋白作为巨噬细胞的趋化因子,因此可能也参与了这一过程。晶体的摄取似乎受到调节机制的控制,因为已观察到调节COM晶体胞吞作用的分子,这一过程与细胞骨架特殊成分的变化有关。总之,粘附和胞吞过程促进了晶体在肾单位中的滞留,而细胞内解构是防止钙在肾脏沉积的一个重要防御因素。