Deciphering cellular heterogeneity in Spodoptera frugiperda midgut cell line through single cell RNA sequencing

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Surjeet Kumar Arya , Douglas A. Harrison , Subba Reddy Palli
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Abstract

Using the 10x Genomics Chromium single-cell RNA sequencing (scRNA-seq) platform, we discovered unexpected heterogeneity in an established cell line developed from the midgut of the Fall armyworm, Spodoptera frugiperda, a major global pest. We analyzed the sequences of 18,794 cells and identified ten unique cellular clusters, including stem cells, enteroblasts, enterocytes and enteroendocrine cells, characterized by the expression of specific marker genes. Additionally, these studies addressed an important knowledge gap by investigating the expression of genes coding for respiratory and midgut membrane insecticide targets classified by the Insecticide Resistance Action Committee. Dual-fluorescence tagging method, fluorescence microscopy and fluorescence-activated cell sorting confirmed the expression of midgut cell type-specific genes. Stem cells were isolated from the heterogeneous population of SfMG-0617 cells. Our results, validated by KEGG and Gene Ontology analyses and supported by Monocle 3.0, advance the fields of midgut cellular biology and establish standards for scRNA-seq studies in non-model organisms.

Abstract Image

通过单细胞 RNA 测序破译弗氏蝶类中肠细胞系的细胞异质性。
利用 10× Genomics Chromium 单细胞 RNA 测序(scRNA-seq)平台,我们在从全球主要害虫--福氏斜纹夜蛾(Spodoptera frugiperda)的中肠中培育的成熟细胞系中发现了意想不到的异质性。我们分析了 18,794 个细胞的序列,发现了十个独特的细胞群,包括干细胞、肠母细胞、鹅口疮细胞和肠内分泌细胞,它们以特定标记基因的表达为特征。此外,这些研究还通过调查被杀虫剂抗药性行动委员会列为呼吸道和中肠膜杀虫剂靶标的编码基因的表达情况,填补了一项重要的知识空白。双荧光标记法、荧光显微镜和荧光激活细胞分选证实了中肠细胞特异性基因的表达。从 SfMG-0617 细胞的异质性群体中分离出了干细胞。我们的研究结果得到了 KEGG 和基因本体分析的验证和 Monocle 3.0 的支持,推动了中肠细胞生物学领域的发展,并为非模式生物的 scRNA-seq 研究建立了标准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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