Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Oncode Institute, Utrecht, The Netherlands.
Dev Dyn. 2021 Nov;250(11):1568-1583. doi: 10.1002/dvdy.346. Epub 2021 May 6.
Nephron progenitor cells (NPCs) undergo a stepwise process to generate all mature nephron structures. Mesenchymal to epithelial transition (MET) is considered a multistep process of NPC differentiation to ensure progressive establishment of new nephrons. However, despite this important role, to date, no marker for NPCs undergoing MET in the nephron exists.
Here, we identify LGR6 as a NPC marker, expressed in very early cap mesenchyme, pre-tubular aggregates, renal vesicles, and in segments of S-shaped bodies, following the trajectory of MET. By using a lineage tracing approach in embryonic explants in combination with confocal imaging and single-cell RNA sequencing, we provide evidence for the multiple fates of LGR6+ cells during embryonic nephrogenesis. Moreover, by using long-term in vivo lineage tracing, we show that postnatal LGR6+ cells are capable of generating the multiple lineages of the nephrons.
Given the profound early mesenchymal expression and MET signature of LGR6 cells, together with the lineage tracing of mesenchymal LGR6 cells, we conclude that LGR6+ cells contribute to all nephrogenic segments by undergoing MET. LGR6+ cells can therefore be considered an early committed NPC population during embryonic and postnatal nephrogenesis with potential regenerative capability.
肾祖细胞 (NPC) 经历一个逐步的过程来生成所有成熟的肾单位结构。间质到上皮的转变 (MET) 被认为是 NPC 分化的多步骤过程,以确保新肾单位的逐步建立。然而,尽管这一作用很重要,但迄今为止,尚无 NPC 经历 MET 生成肾单位的标志物。
在这里,我们确定 LGR6 是 NPC 的标志物,在早期帽状间质、小管前聚集物、肾小泡以及 S 形体的片段中表达,沿着 MET 的轨迹表达。通过在胚胎外植体中使用谱系追踪方法结合共聚焦成像和单细胞 RNA 测序,我们提供了证据证明 LGR6+细胞在胚胎肾发生过程中的多种命运。此外,通过长期体内谱系追踪,我们表明,出生后 LGR6+细胞能够生成肾单位的多个谱系。
鉴于 LGR6 细胞的强烈早期间质表达和 MET 特征,以及对间质 LGR6 细胞的谱系追踪,我们得出结论,LGR6+细胞通过 MET 有助于所有肾发生段。因此,LGR6+细胞可以被认为是胚胎和出生后肾发生过程中的一个早期定向 NPC 群体,具有潜在的再生能力。