Department of Stem Cell Biology and Regenerative Medicine and.
Maternal Fetal Medicine Division, Department of Obstetrics and Gynecology, Keck School of Medicine, University of Southern California, Los Angeles, California.
J Am Soc Nephrol. 2018 Mar;29(3):825-840. doi: 10.1681/ASN.2017091036. Epub 2018 Feb 15.
The nephron is the functional unit of the kidney, but the mechanism of nephron formation during human development is unclear. We conducted a detailed analysis of nephron development in humans and mice by immunolabeling, and we compared human and mouse nephron patterning to describe conserved and divergent features. We created protein localization maps that highlight the emerging patterns along the proximal-distal axis of the developing nephron and benchmark expectations for localization of functionally important transcription factors, which revealed unanticipated cellular diversity. Moreover, we identified a novel nephron subdomain marked by expression that we fate-mapped to the proximal mature nephron. Significant conservation was observed between human and mouse patterning. We also determined the time at which markers for mature nephron cell types first emerge-critical data for the renal organoid field. These findings have conceptual implications for the evolutionary processes driving the diversity of mammalian organ systems. Furthermore, these findings provide practical insights beyond those gained with mouse and rat models that will guide efforts to harness the developmental programs necessary to build human kidney structures.
肾单位是肾脏的功能单位,但人类发育过程中肾单位形成的机制尚不清楚。我们通过免疫标记对人类和小鼠的肾单位发育进行了详细分析,并比较了人类和小鼠的肾单位模式,以描述保守和分歧的特征。我们创建了蛋白质定位图谱,突出了沿发育中肾单位的近-远轴的新兴模式,并为功能重要的转录因子的定位提供了基准预期,这揭示了出人意料的细胞多样性。此外,我们鉴定了一个由 表达标记的新型肾单位亚域,并将其映射到近端成熟肾单位。在人类和小鼠的模式之间观察到显著的保守性。我们还确定了成熟肾单位细胞类型的标记首次出现的时间——这是肾脏类器官领域的关键数据。这些发现对驱动哺乳动物器官系统多样性的进化过程具有概念意义。此外,这些发现提供了超越小鼠和大鼠模型所获得的实用见解,将指导利用构建人类肾脏结构所需的发育程序的努力。