Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA; Kidney Research Institute, Seattle, Washington, USA.
Kidney Research Institute, Seattle, Washington, USA.
Kidney Int. 2022 May;101(5):1017-1026. doi: 10.1016/j.kint.2022.01.033. Epub 2022 Feb 26.
Collapsing glomerulopathy is a histologically distinct variant of focal and segmental glomerulosclerosis that presents with heavy proteinuria and portends a poor prognosis. Collapsing glomerulopathy can be triggered by viral infections such as HIV or SARS-CoV-2. Transcriptional profiling of collapsing glomerulopathy lesions is difficult since only a few glomeruli may exhibit this histology within a kidney biopsy and the mechanisms driving this heterogeneity are unknown. Therefore, we used recently developed digital spatial profiling (DSP) technology which permits quantification of mRNA at the level of individual glomeruli. Using DSP, we profiled 1,852 transcripts in glomeruli isolated from formalin fixed paraffin embedded sections from HIV or SARS-CoV-2-infected patients with biopsy-confirmed collapsing glomerulopathy and used normal biopsy sections as controls. Even though glomeruli with collapsing features appeared histologically similar across both groups of patients by light microscopy, the increased resolution of DSP uncovered intra- and inter-patient heterogeneity in glomerular transcriptional profiles that were missed in early laser capture microdissection studies of pooled glomeruli. Focused validation using immunohistochemistry and RNA in situ hybridization showed good concordance with DSP results. Thus, DSP represents a powerful method to dissect transcriptional programs of pathologically discernible kidney lesions.
塌陷性肾小球病是局灶节段性肾小球硬化的一种组织学上明显不同的变异型,表现为大量蛋白尿,并预示预后不良。塌陷性肾小球病可由 HIV 或 SARS-CoV-2 等病毒感染引发。由于在肾活检中只有少数肾小球可能表现出这种组织学特征,并且驱动这种异质性的机制尚不清楚,因此对塌陷性肾小球病病变进行转录谱分析具有一定难度。因此,我们使用了最近开发的数字空间分析 (DSP) 技术,该技术可以在单个肾小球水平上定量检测 mRNA。利用 DSP,我们对来自 HIV 或 SARS-CoV-2 感染患者的福尔马林固定石蜡包埋切片中分离的肾小球进行了 1852 个转录本的分析,这些患者经活检证实患有塌陷性肾小球病,正常活检切片作为对照。尽管两组患者的光镜下塌陷特征的肾小球在组织学上看起来相似,但 DSP 分辨率的提高揭示了肾小球转录谱中的内在和患者间异质性,这在早期对 pooled 肾小球进行激光捕获微切割研究中被忽略了。使用免疫组织化学和 RNA 原位杂交进行的重点验证显示与 DSP 结果具有良好的一致性。因此,DSP 代表了一种剖析病理性可识别肾脏病变转录程序的强大方法。