单细胞分辨率下果蝇脑中的砷毒性。

IF 4.6 Q2 TOXICOLOGY
Frontiers in toxicology Pub Date : 2025-07-10 eCollection Date: 2025-01-01 DOI:10.3389/ftox.2025.1636431
Anurag Chaturvedi, Vijay Shankar, Bibhu Simkhada, Rachel A Lyman, Patrick Freymuth, Elisabeth Howansky, Katelynne M Collins, Trudy F C Mackay, Robert R H Anholt
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引用次数: 0

摘要

砷是一种普遍存在的环境毒物,具有有害的生理效应,包括神经毒性。砷诱导的基因表达在大脑中的调节在人类受试者中还不能轻易研究。然而,果蝇允许在单次分析中对整个大脑的单细胞分辨率的神经毒素转录反应进行量化。我们将黑腹果蝇暴露于慢性剂量的NaAsO2中,该剂量不会导致快速死亡,并测量了生存率和负地向性,作为感觉运动整合的代理。雌性比雄性存活时间长,但在攀爬能力上表现出较早的生理损伤。单核RNA测序显示广泛的性别拮抗转录反应,基因表达调节在雌性偏向神经元细胞群和雄性偏向神经胶质细胞。然而,差异表达的基因暗示着相似的生物学途径。神经系统基本过程的进化守恒使我们能够将砷诱导的转录物丰度变化从果蝇模型转化为同源的人类神经遗传网络。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Arsenic toxicity in the Drosophila brain at single cell resolution.

Arsenic is an ubiquitous environmental toxicant with harmful physiological effects, including neurotoxicity. Modulation of arsenic-induced gene expression in the brain cannot be readily studied in human subjects. However, Drosophila allows quantification of transcriptional responses to neurotoxins at single cell resolution across the entire brain in a single analysis. We exposed Drosophila melanogaster to a chronic dose of NaAsO2 that does not cause rapid lethality and measured survival and negative geotaxis as a proxy of sensorimotor integration. Females survive longer than males but show earlier physiological impairment in climbing ability. Single-nuclei RNA sequencing showed widespread sex-antagonistic transcriptional responses with modulation of gene expression in females biased toward neuronal cell populations and in males toward glial cells. However, differentially expressed genes implicate similar biological pathways. Evolutionary conservation of fundamental processes of the nervous system enabled us to translate arsenic-induced changes in transcript abundances from the Drosophila model to orthologous human neurogenetic networks.

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来源期刊
CiteScore
3.80
自引率
0.00%
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审稿时长
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