Experimental Nephrology, Division of Nephrology, Department of Internal Medicine III, University Hospital Carl Gustav Carus at the Technische Universität Dresden, Dresden, Germany.
Institute of Physiology, University Hospital Carl Gustav Carus at the Technische Universität Dresden, Dresden, Germany.
Am J Physiol Renal Physiol. 2021 Sep 1;321(3):F378-F388. doi: 10.1152/ajprenal.00151.2021. Epub 2021 Aug 2.
Developmentally heterogeneous renin-expressing cells serve as progenitors for mural, glomerular, and tubular cells during nephrogenesis and are collectively termed renin lineage cells (RLCs). In this study, we quantified different renal vascular and tubular cell types based on specific markers and assessed proliferation and de novo differentiation in the RLC population. We used kidney sections of mRenCre-mT/mG mice throughout nephrogenesis. Marker positivity was evaluated in whole digitalized sections. At , RLCs appeared in the developing kidney, and the expression of all stained markers in RLCs was observed. The proliferation rate of RLCs did not differ from the proliferation rate of non-RLCs. RLCs expanded mainly by de novo differentiation (neogenesis). Fractions of RLCs originating from the stromal progenitors of the metanephric mesenchyme (renin-producing cells, vascular smooth muscle cells, and mesangial cells) decreased during nephrogenesis. In contrast, aquaporin-2-positive RLCs in the collecting duct system, which embryonically emerges almost exclusively from the ureteric bud, expanded postpartum. The cubilin-positive RLC fraction in the proximal tubule, deriving from the cap mesenchyme, remained constant. In summary, RLCs were continuously detectable in the vascular and tubular compartments of the kidney during nephrogenesis. Therein, various patterns of RLC differentiation that depend on the embryonic origin of the cells were identified. The unifying feature of the renal renin lineage cells (RLCs) is their origin from renin-expressing progenitors. RLCs evolve to an embryologically heterogeneous large population in structures with different ancestry. RLCs are also targets for the widely used renin-angiotensin-system blockers, which modulate their phenotype. Unveiling the different differentiation patterns of RLCs in the developing kidney contributes to understanding changes in their cell fate in response to homeostatic challenges and the use of antihypertensive drugs.
在肾发生过程中,发育异质性的肾素表达细胞作为壁层、肾小球和管状细胞的祖细胞,统称为肾素谱系细胞(RLC)。在这项研究中,我们根据特定的标记物对不同的肾血管和管状细胞类型进行了定量,并评估了 RLC 群体中的增殖和新分化。我们在整个肾发生过程中使用了 mRenCre-mT/mG 小鼠的肾组织切片。在整个数字化切片中评估了标记物的阳性率。在 ,RLC 出现在发育中的肾脏中,并且观察到 RLC 中所有染色标记物的表达。RLC 的增殖率与非 RLC 的增殖率没有差异。RLC 主要通过新分化(新生)来扩增。肾间质祖细胞(产生肾素的细胞、血管平滑肌细胞和系膜细胞)衍生的 RLC 分数在肾发生过程中减少。相比之下,在后生期,在集合管系统中发现的水通道蛋白 2 阳性 RLC 大量扩增,而后者几乎仅从输尿管芽中出现。来源于帽状间充质的近端小管中,双氢吡啶结合蛋白 2 阳性 RLC 分数保持不变。总之,在肾发生过程中,RLC 可在肾血管和管状腔室中持续检测到。在此过程中,确定了依赖于细胞胚胎起源的各种 RLC 分化模式。肾素谱系细胞(RLC)的统一特征是它们起源于表达肾素的祖细胞。RLC 进化为具有不同祖源的结构中具有胚胎学异质性的大群体。RLC 也是广泛使用的肾素-血管紧张素系统阻滞剂的靶标,这些阻滞剂可调节其表型。揭示发育中肾脏中 RLC 的不同分化模式有助于了解它们在应对体内平衡挑战和使用抗高血压药物时的细胞命运变化。