Schmidt-Ott Kai M, Yang Jun, Chen Xia, Wang Howard, Paragas Neal, Mori Kiyoshi, Li Jau-Yi, Lu Benson, Costantini Frank, Schiffer Mario, Bottinger Erwin, Barasch Jonathan
Department of Medicine, Columbia University College of Physicians and Surgeons, 630 W. 168th Street, New York, NY 10032, USA.
J Am Soc Nephrol. 2005 Jul;16(7):1993-2002. doi: 10.1681/ASN.2004121127. Epub 2005 May 25.
Mammalian nephrogenesis depends on the interaction between the ureteric bud and the metanephric mesenchyme. As the ureteric bud undergoes branching and segmentation, the stalks differentiate into the collecting system of the mature kidney, while the tip cells interact with the adjacent cells of the metanephric mesenchyme, inducing their conversion into nephrons. This induction is mediated by secreted factors. For identifying novel mediators, the tips of the ureteric tree were isolated and microarray analyses were performed using manually refined, multistep gene ontology annotations. For identifying conserved factors, two databases were developed, one from mouse E12.5 and one from rat E13.5 ureteric buds. The overlap of mouse and rat data sets yielded 20 different transcripts that were enriched in the ureteric bud compared with metanephric mesenchyme and predicted to code for secreted proteins. Real-time reverse transcriptase-PCR and in situ hybridization confirmed these identifications. One of the genes that was highly specific to the ureteric bud tip was cytokine-like factor 1 (CLF-1). Recombinant CLF-1 in complex with its physiologic ligand, cardiotrophin-like cytokine (CLC), triggered phosphorylation of signal transducer and activator of transcription 3 in mesenchyme, a pathway characteristic of mesenchymal-to-epithelial conversion. Indeed, when applied to isolated rat metanephric mesenchyme, CLF-1/CLC (3 nM) induced mature nephron structures expressing glomerular and tubular markers. These results underline the power of this first comprehensive gene expression analysis of the ureteric bud tip to identify bioactive molecules.
哺乳动物的肾发生依赖于输尿管芽和后肾间充质之间的相互作用。随着输尿管芽发生分支和分段,其茎分化为成熟肾脏的集合系统,而顶端细胞与后肾间充质的相邻细胞相互作用,诱导它们转化为肾单位。这种诱导是由分泌因子介导的。为了鉴定新的介质,分离了输尿管树的顶端,并使用手动优化的多步骤基因本体注释进行了微阵列分析。为了鉴定保守因子,开发了两个数据库,一个来自小鼠E12.5输尿管芽,另一个来自大鼠E13.5输尿管芽。小鼠和大鼠数据集的重叠产生了20种不同的转录本,与后肾间充质相比,这些转录本在输尿管芽中富集,并预测编码分泌蛋白。实时逆转录聚合酶链反应和原位杂交证实了这些鉴定。输尿管芽顶端高度特异的基因之一是细胞因子样因子1(CLF-1)。重组CLF-1与其生理配体心肌营养素样细胞因子(CLC)形成复合物,触发间充质中转录信号转导子和激活子3的磷酸化,这是间充质向上皮转化的特征途径。事实上,当应用于分离的大鼠后肾间充质时,CLF-1/CLC(3 nM)诱导表达肾小球和肾小管标志物的成熟肾单位结构。这些结果强调了对输尿管芽顶端进行首次全面基因表达分析以鉴定生物活性分子的能力。