Little Melissa Helen, Kairath Pamela
Murdoch Children's Research Institute, Melbourne, Australia; and
Department of Pediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Melbourne, Australia.
J Am Soc Nephrol. 2017 Jan;28(1):34-46. doi: 10.1681/ASN.2016070748. Epub 2016 Oct 26.
Over a decade ago, it was proposed that the regulation of tubular repair in the kidney might involve the recapitulation of developmental pathways. Although the kidney cannot generate new nephrons after birth, suggesting a low level of regenerative competence, the tubular epithelial cells of the nephrons can proliferate to repair the damage after AKI. However, the debate continues over whether this repair involves a persistent progenitor population or any mature epithelial cell remaining after injury. Recent reports have highlighted the expression of Sox9, a transcription factor critical for normal kidney development, during postnatal epithelial repair in the kidney. Indeed, the proliferative response of the epithelium involves expression of several pathways previously described as being involved in kidney development. In some instances, these pathways are also apparently involved in the maladaptive responses observed after repeated injury. Whether development and repair in the kidney are the same processes or we are misinterpreting the similar expression of genes under different circumstances remains unknown. Here, we review the evidence for this link, concluding that such parallels in expression may more correctly represent the use of the same pathways in a distinct context, likely triggered by similar stressors.
十多年前,有人提出肾脏中肾小管修复的调控可能涉及发育途径的重演。尽管出生后肾脏无法生成新的肾单位,这表明其再生能力较低,但肾单位的肾小管上皮细胞可以增殖以修复急性肾损伤后的损伤。然而,关于这种修复是涉及持续存在的祖细胞群体还是损伤后残留的任何成熟上皮细胞,争论仍在继续。最近的报告强调了Sox9(一种对正常肾脏发育至关重要的转录因子)在出生后肾脏上皮修复过程中的表达。事实上,上皮细胞的增殖反应涉及先前描述的几种参与肾脏发育的途径的表达。在某些情况下,这些途径显然也参与了反复损伤后观察到的适应性不良反应。肾脏的发育和修复是相同的过程,还是我们在不同情况下对相似基因表达的解读有误,目前尚不清楚。在这里,我们回顾了这种联系的证据,得出结论认为,这种表达上的相似性可能更正确地代表了相同途径在不同背景下的使用,可能是由相似的应激源触发的。