Avner E D, Ellis D, Temple T, Jaffe R
In Vitro. 1982 Aug;18(8):675-82. doi: 10.1007/BF02796422.
A new mouse metanephric organ culture system has been developed to study mammalian renal development. The system permits in vitro organotypic differentiation in a serum-free, hormone supplemented medium consisting of Dulbecco's minimal essential medium (MEM) and Ham's F12 medium supplemented with insulin, 5 microgram/ml; PGE1, 25 ng/ml; T3, 3.2 pg/ml; hydrocortisone, 5 microgram/ml; and transferrin, 5 microgram/ml. In this system, metanephric development continues morphologically beyond the S-shaped tubule stage. A well differentiated proximal tubule forms with a well defined brush border, specialized intercellular connections, and an apical endocytic network. In addition, a unique devascularized glomerulus, with highly differentiated podocytes surrounding areas of basement membrane, forms entirely from epithelial elements. The present organ culture model goes beyond the limitations of previously described systems in that it does not require separation of nephrogenic blastema from ureteric bud, nor require animal serum or nonspecific tissue extracts for metanephric development. The model is thus suited for morphological, biochemical, and endocrinological study of normal and abnormal renal organogenesis.
一种新的小鼠后肾器官培养系统已被开发出来用于研究哺乳动物肾脏发育。该系统允许在一种无血清、添加激素的培养基中进行体外器官型分化,这种培养基由杜尔贝科改良伊格尔培养基(MEM)和哈姆F12培养基组成,并添加了胰岛素(5微克/毫升)、前列腺素E1(25纳克/毫升)、三碘甲状腺原氨酸(3.2皮克/毫升)、氢化可的松(5微克/毫升)和转铁蛋白(5微克/毫升)。在这个系统中,后肾发育在形态学上会持续超过S形小管阶段。会形成一个分化良好的近端小管,具有明确的刷状缘、特化的细胞间连接和顶端内吞网络。此外,一个独特的无血管肾小球会完全由上皮成分形成,其周围有高度分化的足细胞围绕着基底膜区域。目前的器官培养模型超越了先前描述系统的局限性,因为它既不需要将生肾组织与输尿管芽分离,也不需要动物血清或非特异性组织提取物来进行后肾发育。因此,该模型适合用于正常和异常肾脏器官发生的形态学、生物化学和内分泌学研究。