A comparative transcriptomics analysis of mammalian and non-mammalian acute kidney injury (AKI) models.

IF 4.6 2区 生物学 Q2 CELL BIOLOGY
Frontiers in Cell and Developmental Biology Pub Date : 2025-09-26 eCollection Date: 2025-01-01 DOI:10.3389/fcell.2025.1653967
Matthew R Hawkins, Diana Cervera, Tiffany M Tang, Rebecca A Wingert
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引用次数: 0

Abstract

Introduction: Acute kidney injury (AKI) is a complex clinical condition characterized by decline in renal function and widespread transcriptional dysregulation. While transcriptomic studies that compare human and other mammalian models of AKI have provided insight, much less is known about commonalities and contrasts between mammalian models and nontraditional and regenerative laboratory models. Understanding these molecular level responses to injury in both regenerative and non-regenerative models may reveal conserved and unique pathways in renal repair.

Methods: To investigate transcriptional responses to AKI across species, we incorporated newly available RNA-seq data from zebrafish, axolotl, and spiny mouse models into an expanded cross-species comparative analysis. These were analyzed alongside existing and previously analyzed data from both human and mouse (Mus) models. Differential gene expression and gene-ontology (GO) enrichment analyses we utilized to identify conserved and regeneration-specific during injury and recovery phases.

Results: Comparative transcriptomic analysis revealed distinct transcriptional programs in each species during AKI, including both shared and species-specific responses. Of note, zebrafish show differential expression of apolipoproteins, molecules of increasing interest to the greater field of nephrology. In the recovery setting, we show that animals with regenerative capacity have conserved and divergent transcriptional programs.

Discussion: Our findings demonstrate that non-traditional animal models of AKI, such as zebrafish, axolotls, and spiny mice, provide valuable insights into the molecular basis of kidney regeneration. The identification of conserved and divergent injury responses suggests evolutionary conservation in core AKI mechanisms, while also pointing to regeneration-associated transcriptional programs that could inform future therapeutic strategies. This work underscores the importance of using non-traditional models as well as the value in comparative analysis with traditional models and clinical data.

哺乳动物和非哺乳动物急性肾损伤(AKI)模型的转录组学比较分析。
急性肾损伤(AKI)是一种复杂的临床疾病,以肾功能下降和广泛的转录失调为特征。虽然比较人类和其他哺乳动物AKI模型的转录组学研究提供了一些见解,但对哺乳动物模型与非传统和再生实验室模型之间的共性和对比知之甚少。了解再生和非再生模型中对损伤的分子水平反应可能会揭示肾脏修复中保守和独特的途径。方法:为了研究跨物种对AKI的转录反应,我们将来自斑马鱼、美西螈和刺鼠模型的最新RNA-seq数据纳入扩展的跨物种比较分析中。这些数据与来自人类和小鼠(Mus)模型的现有和先前分析的数据一起进行了分析。我们利用差异基因表达和基因本体(GO)富集分析来识别损伤和恢复阶段的保守性和再生特异性。结果:比较转录组学分析揭示了AKI期间每个物种不同的转录程序,包括共享反应和物种特异性反应。值得注意的是,斑马鱼表现出载脂蛋白的差异表达,载脂蛋白分子对肾脏学的更大领域越来越感兴趣。在恢复环境中,我们发现具有再生能力的动物具有保守的和不同的转录程序。讨论:我们的研究结果表明,非传统的AKI动物模型,如斑马鱼、蝾螈和刺鼠,为肾脏再生的分子基础提供了有价值的见解。保守性和发散性损伤反应的鉴定表明核心AKI机制的进化保守性,同时也指出再生相关的转录程序可以为未来的治疗策略提供信息。这项工作强调了使用非传统模型的重要性,以及与传统模型和临床数据进行比较分析的价值。
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来源期刊
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
9.70
自引率
3.60%
发文量
2531
审稿时长
12 weeks
期刊介绍: Frontiers in Cell and Developmental Biology is a broad-scope, interdisciplinary open-access journal, focusing on the fundamental processes of life, led by Prof Amanda Fisher and supported by a geographically diverse, high-quality editorial board. The journal welcomes submissions on a wide spectrum of cell and developmental biology, covering intracellular and extracellular dynamics, with sections focusing on signaling, adhesion, migration, cell death and survival and membrane trafficking. Additionally, the journal offers sections dedicated to the cutting edge of fundamental and translational research in molecular medicine and stem cell biology. With a collaborative, rigorous and transparent peer-review, the journal produces the highest scientific quality in both fundamental and applied research, and advanced article level metrics measure the real-time impact and influence of each publication.
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