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星形细胞表面抗原 2 和其他潜在的肠道神经胶质细胞表面标记物在小鼠结肠中的表达。

Astrocyte Cell Surface Antigen 2 and Other Potential Cell Surface Markers of Enteric glia in the Mouse Colon.

机构信息

Department of Physiology and Neuroscience program, 3078Michigan State University, East Lansing, MI, USA.

出版信息

ASN Neuro. 2022 Jan-Dec;14:17590914221083203. doi: 10.1177/17590914221083203.

DOI:10.1177/17590914221083203
PMID:35593118
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9125112/
Abstract

Enteric glia regulate gut functions in health and disease through diverse interactions with neurons and immune cells. Intracellular localization of traditional markers of enteric glia such as GFAP, s100b, and Sox10 makes them incompatible for studies that require antigen localization at the cell surface. Thus, new tools are needed for probing the heterogeneous roles of enteric glia at the protein, cell, and functional levels. Here we selected several cell surface antigens including Astrocyte Cell Surface Marker 2 (ACSA2), Cluster of differentiation 9 (CD9), lysophosphatidic acid receptor 1 (LPAR1), and Proteolipid protein 1 (PLP1) as potential markers of enteric glia. We tested their specificity for enteric glia using published single-cell/-nuclei and glia-specific translating mRNA enriched transcriptome datasets, immunolabeling, and flow cytometry. The data show that ACSA2 is a specific marker of mucosal and myenteric glia while other markers are suitable for identifying all subpopulations of enteric glia (LPAR1), glia and immune cells (CD9), or are not suitable for cell-surface labeling (PLP1). These new tools will be useful for future work focused on understanding specific glial functions in health and disease.This study identifies astrocyte cell surface antigen 2 as a novel marker of myenteric glia in the intestine. This, in combination with other markers identified in this study, could be used for selective targeting of enteric glia.

摘要

肠胶质细胞通过与神经元和免疫细胞的多种相互作用来调节肠道功能的健康和疾病。传统的肠胶质细胞标志物如 GFAP、s100b 和 Sox10 的细胞内定位使得它们不适合需要抗原在细胞表面定位的研究。因此,需要新的工具来探测肠胶质细胞在蛋白质、细胞和功能水平上的异质作用。在这里,我们选择了几种细胞表面抗原,包括星形胶质细胞表面标志物 2(ACSA2)、分化簇 9(CD9)、溶血磷脂酸受体 1(LPAR1)和蛋白脂质蛋白 1(PLP1),作为肠胶质细胞的潜在标志物。我们使用已发表的单细胞/核和胶质特异性翻译 mRNA 富集转录组数据集、免疫标记和流式细胞术来测试它们对肠胶质细胞的特异性。数据表明,ACSA2 是黏膜和肌间胶质细胞的特异性标志物,而其他标志物适合识别肠胶质细胞的所有亚群(LPAR1)、胶质细胞和免疫细胞(CD9),或者不适合细胞表面标记(PLP1)。这些新工具将有助于未来的研究,以了解健康和疾病中特定胶质细胞的功能。本研究鉴定了星形胶质细胞表面抗原 2 是肠道肌间胶质细胞的一个新标志物。这与本研究中鉴定的其他标志物结合使用,可用于肠胶质细胞的选择性靶向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afed/9125112/c0cf3fbb7371/10.1177_17590914221083203-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afed/9125112/1fbf6f47af7b/10.1177_17590914221083203-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afed/9125112/4a6b5c172c6a/10.1177_17590914221083203-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afed/9125112/8cb92c838275/10.1177_17590914221083203-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afed/9125112/03a5a3558a9b/10.1177_17590914221083203-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afed/9125112/4cedf23a5f4f/10.1177_17590914221083203-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afed/9125112/c0cf3fbb7371/10.1177_17590914221083203-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afed/9125112/1fbf6f47af7b/10.1177_17590914221083203-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afed/9125112/4a6b5c172c6a/10.1177_17590914221083203-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afed/9125112/8cb92c838275/10.1177_17590914221083203-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afed/9125112/03a5a3558a9b/10.1177_17590914221083203-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afed/9125112/4cedf23a5f4f/10.1177_17590914221083203-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afed/9125112/c0cf3fbb7371/10.1177_17590914221083203-fig6.jpg

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Regulation of intestinal immunity and tissue repair by enteric glia.肠胶质细胞对肠道免疫和组织修复的调节作用。
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Circuit-specific enteric glia regulate intestinal motor neurocircuits.特定回路的肠胶质细胞调节肠道运动神经回路。
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