Festa Beatrice Paola, Berquez Marine, Nieri Daniela, Luciani Alessandro
Institute of Physiology, Mechanisms of Inherited Kidney Disorders Group, University of Zurich, Zurich, Switzerland.
Rev Physiol Biochem Pharmacol. 2023;185:233-257. doi: 10.1007/112_2020_57.
Epithelial cells that line the proximal tubule of the kidney rely on an intertwined ecosystem of vesicular membrane trafficking pathways to ensure the reabsorption of essential nutrients. To function effectively and to achieve homeostasis, these specialized cells require the sorting and recycling of a wide array of cell surface proteins within the endolysosomal network, including signaling receptors, nutrient transporters, ion channels, and polarity markers. The dysregulation of the endolysosomal system can lead to a generalized proximal tubule dysfunction, ultimately causing severe metabolic complications and kidney disease.In this chapter, we highlight the biological functions of the genes that code endolysosomal proteins from the perspective of understanding - and potentially reversing - the pathophysiology of endolysosomal disorders affecting the proximal tubule of the kidney. These insights might ultimately lead to potential treatments for currently intractable diseases and transform our ability to regulate kidney homeostasis and health.
肾脏近端小管内衬的上皮细胞依赖于相互交织的囊泡膜运输途径生态系统,以确保必需营养物质的重吸收。为了有效发挥功能并实现内环境稳态,这些特殊细胞需要在内溶酶体网络内对多种细胞表面蛋白进行分类和循环利用,包括信号受体、营养转运体、离子通道和极性标记物。内溶酶体系统的失调可导致广泛性近端小管功能障碍,最终引发严重的代谢并发症和肾脏疾病。在本章中,我们从理解并可能逆转影响肾脏近端小管的内溶酶体疾病的病理生理学角度,突出编码内溶酶体蛋白的基因的生物学功能。这些见解最终可能会带来针对目前难以治疗的疾病的潜在疗法,并改变我们调节肾脏内环境稳态和健康的能力。