DiKun Krysta M, Gudas Lorraine J
Department of Pharmacology, Weill Cornell Medical College of Cornell University, New York, NY, USA; New York Presbyterian Hospital, New York, NY, USA; Weill Cornell Graduate School of Medical Sciences, New York, NY, USA.
Department of Pharmacology, Weill Cornell Medical College of Cornell University, New York, NY, USA; Department of Urology, Weill Cornell Medicine, New York, NY, USA; New York Presbyterian Hospital, New York, NY, USA; Weill Cornell Graduate School of Medical Sciences, New York, NY, USA.
Pharmacol Ther. 2023 Aug;248:108481. doi: 10.1016/j.pharmthera.2023.108481. Epub 2023 Jun 17.
Vitamin A (VA, retinol) and its metabolites (commonly called retinoids) are required for the proper development of the kidney during embryogenesis, but retinoids also play key roles in the function and repair of the kidney in adults. Kidneys filter 180-200 liters of blood per day and each kidney contains approximately 1 million nephrons, which are often referred to as the 'functional units' of the kidney. Each nephron consists of a glomerulus and a series of tubules (proximal tubule, loop of Henle, distal tubule, and collecting duct) surrounded by a network of capillaries. VA is stored in the liver and converted to active metabolites, most notably retinoic acid (RA), which acts as an agonist for the retinoic acid receptors ((RARs α, β, and γ) to regulate gene transcription. In this review we discuss some of the actions of retinoids in the kidney after injury. For example, in an ischemia-reperfusion model in mice, injury-associated loss of proximal tubule (PT) differentiation markers occurs, followed by re-expression of these differentiation markers during PT repair. Notably, healthy proximal tubules express ALDH1a2, the enzyme that metabolizes retinaldehyde to RA, but transiently lose ALDH1a2 expression after injury, while nearby myofibroblasts transiently acquire RA-producing capabilities after injury. These results indicate that RA is important for renal tubular injury repair and that compensatory mechanisms exist for the generation of endogenous RA by other cell types upon proximal tubule injury. ALDH1a2 levels also increase in podocytes, epithelial cells of the glomeruli, after injury, and RA promotes podocyte differentiation. We also review the ability of exogenous, pharmacological doses of RA and receptor selective retinoids to treat numerous kidney diseases, including kidney cancer and diabetic kidney disease, and the emerging genetic evidence for the importance of retinoids and their receptors in maintaining or restoring kidney function after injury. In general, RA has a protective effect on the kidney after various types of injuries (eg. ischemia, cytotoxic actions of chemicals, hyperglycemia related to diabetes). As more research into the actions of each of the three RARs in the kidney is carried out, a greater understanding of the actions of vitamin A is likely to lead to new insights into the pathology of kidney disorders and the development of new therapies for kidney diseases.
维生素A(VA,视黄醇)及其代谢产物(通常称为类视黄醇)在胚胎发育过程中对肾脏的正常发育是必需的,但类视黄醇在成体肾脏的功能和修复中也起着关键作用。肾脏每天过滤180 - 200升血液,每个肾脏包含大约100万个肾单位,这些肾单位通常被称为肾脏的“功能单位”。每个肾单位由一个肾小球和一系列被毛细血管网络包围的肾小管(近端小管、髓袢、远端小管和集合管)组成。VA储存在肝脏中并转化为活性代谢产物,最显著的是视黄酸(RA),它作为视黄酸受体(RARα、β和γ)的激动剂来调节基因转录。在本综述中,我们讨论了类视黄醇在肾脏损伤后的一些作用。例如,在小鼠的缺血再灌注模型中,近端小管(PT)分化标志物会伴随损伤而丢失,随后在PT修复过程中这些分化标志物会重新表达。值得注意的是,健康的近端小管表达ALDH1a2,即一种将视黄醛代谢为RA的酶,但在损伤后会短暂失去ALDH1a2表达,而附近的成肌纤维细胞在损伤后会短暂获得产生RA的能力。这些结果表明RA对肾小管损伤修复很重要,并且在近端小管损伤时其他细胞类型存在产生内源性RA的代偿机制。损伤后,肾小球的上皮细胞足细胞中的ALDH1a2水平也会升高,并且RA促进足细胞分化。我们还综述了外源性、药理学剂量的RA和受体选择性类视黄醇治疗多种肾脏疾病(包括肾癌和糖尿病肾病)的能力,以及类视黄醇及其受体在损伤后维持或恢复肾功能方面重要性的新出现的遗传学证据。一般来说,RA在各种类型的损伤(如缺血、化学物质的细胞毒性作用、与糖尿病相关的高血糖)后对肾脏具有保护作用。随着对三种RARs在肾脏中各自作用的更多研究开展,对维生素A作用的更深入理解可能会为肾脏疾病的病理学带来新的见解,并推动肾脏疾病新疗法的开发。