Pietilä Ilkka, Vainio Seppo J
Oulu Center for Cell-Matrix Research, Biocenter and Infotech Oulu, Laboratory of Developmental Biology, Intelligent Systems, Faculty of Biochemistry and Molecular Medicine, University of Oulu, Oulu, Finland.
Nephron Exp Nephrol. 2014;126(2):40. doi: 10.1159/000360659. Epub 2014 May 19.
Kidney diseases are worldwide public health problems with a high cost and increasing incidence. By revealing the genetic and cellular mechanism behind mammalian kidney development, better diagnostic methods and novel therapies can be expected to be developed. The mammalian kidney is a typical organ that develops on the basis of sequential and reciprocal cell and tissue interactions. Functional genetic analysis has identified that genes from different classes are involved in the construction of the kidney and the same genes are also connected to the development of diseases.
This review gives an overview of the basics of kidney ontogeny, from identification of the primary kidney cell to inductive signals of ureter budding and formation of the segmented nephron. We also go through some of the key factors involved in the control of morphogenesis.
Despite the wealth of accumulated data on nephron development, including progenitor cell control factors and inductive signals, many of the detailed mechanisms remain to be revealed.
肾脏疾病是全球性的公共卫生问题,成本高昂且发病率不断上升。通过揭示哺乳动物肾脏发育背后的遗传和细胞机制,有望开发出更好的诊断方法和新型疗法。哺乳动物的肾脏是一个典型的器官,它基于细胞和组织的顺序性和相互作用而发育。功能遗传学分析已经确定,不同类别的基因参与了肾脏的构建,并且相同的基因也与疾病的发展有关。
本综述概述了肾脏个体发生的基础知识,从原肾细胞的识别到输尿管芽生的诱导信号以及分段肾单位的形成。我们还梳理了一些参与形态发生控制的关键因素。
尽管在肾单位发育方面积累了大量数据,包括祖细胞控制因子和诱导信号,但许多详细机制仍有待揭示。