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肾小球和皮质小管间质性基因在肾毒性血清肾炎发展中的时间调控。

Temporal Regulation of Glomerular and Cortical Tubulointerstitial Genes Involved in the Development of Nephrotoxic Serum Nephritis.

机构信息

Novo Nordisk A/S, Måløv, Denmark.

Department of Veterinary Disease Biology, University of Copenhagen, Copenhagen, Denmark.

出版信息

Nephron. 2018;140(3):218-230. doi: 10.1159/000492294. Epub 2018 Sep 11.

DOI:10.1159/000492294
PMID:30205387
Abstract

BACKGROUND/AIMS: Murine nephrotoxic nephritis (NTN) is a well-established model resembling chronic kidney disease. Investigating gene expression patterns separately in the glomerular and cortical tubulointerstitial structure could provide new knowledge about structure-specific changes in expression of genes in the NTN model.

METHODS

Glomerular, cortical tubulointerstitial and whole kidney tissues from mice subjected to nephrotoxic serum (NTS) or phosphate buffered saline (PBS) were collected on day 7, 21 and 42 using laser microdissection (LMD). Total RNA was extracted and subjected to nCounter NanoString. Histology, immunohistochemistry, in situ hybridization and/or quantitative real time PCR (qRT PCR) were performed to confirm regulation of selected genes.

RESULTS

LMD provided detailed information about genes that were regulated differently between structures over time. Some of the fibrotic and inflammatory genes (Col1a1, Col3a1 and Ccl2) were upregulated in both structures, whereas other genes such as Spp1 and Grem1 were differentially regulated suggesting spatial pathogenic mechanisms in the kidney. Downregulation of cortical tubulointerstitium genes involved in iron metabolism was detected along with iron accumulation.

CONCLUSION

This study demonstrates several regulated genes in pathways important for the pathogenesis of the NTN model and that LMD identifies structure-specific changes in gene expression during disease development. Furthermore, this study shows the benefits of isolating glomeruli and cortical tubulointerstitium in order to identify gene regulation.

摘要

背景/目的:小鼠肾毒性肾炎(NTN)是一种成熟的类似于慢性肾脏病的模型。分别研究肾小球和皮质肾小管间质结构中的基因表达模式,可以提供关于 NTN 模型中基因表达的结构特异性变化的新知识。

方法

使用激光微切割(LMD)在第 7、21 和 42 天收集接受肾毒性血清(NTS)或磷酸盐缓冲盐水(PBS)的小鼠的肾小球、皮质肾小管间质和整个肾脏组织。提取总 RNA,并进行 nCounter NanoString 分析。进行组织学、免疫组织化学、原位杂交和/或实时定量 PCR(qRT-PCR)以确认选定基因的调控。

结果

LMD 提供了关于不同结构之间随时间变化的基因调节的详细信息。一些纤维化和炎症基因(Col1a1、Col3a1 和 Ccl2)在两个结构中均上调,而其他基因,如 Spp1 和 Grem1,则表现出不同的调节,表明肾脏中存在空间发病机制。还检测到涉及铁代谢的皮质肾小管间质基因下调以及铁积累。

结论

本研究证明了 NTN 模型发病机制中几个重要途径的调节基因,并且 LMD 确定了疾病发展过程中基因表达的结构特异性变化。此外,本研究表明分离肾小球和皮质肾小管间质以识别基因调节的益处。

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