CPHNet: a novel pipeline for anti-HAPE drug screening via deep learning-based Cell Painting scoring.

IF 5.8 2区 医学 Q1 Medicine Respiratory Research Pub Date : 2025-03-08 DOI:10.1186/s12931-025-03173-1
De-Zhi Sun, Xi-Ru Yang, Cong-Shu Huang, Zhi-Jie Bai, Pan Shen, Zhe-Xin Ni, Chao-Ji Huang-Fu, Yang-Yi Hu, Ning-Ning Wang, Xiang-Lin Tang, Yong-Fang Li, Yue Gao, Wei Zhou
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Abstract

Background: High altitude pulmonary edema (HAPE) poses a significant medical challenge to individuals ascending rapidly to high altitudes. Hypoxia-induced cellular morphological changes in the alveolar-capillary barrier such as mitochondrial structural alterations and cytoskeletal reorganization, play a crucial role in the pathogenesis of HAPE. These morphological changes are critical in understanding the cellular response to hypoxia and represent potential therapeutic targets. However, there is still a lack of effective and valid drug discovery strategies for anti-HAPE treatments based on these cellular morphological features. This study aims to develop a pipeline that focuses on morphological alterations in Cell Painting images to identify potential therapeutic agents for HAPE interventions.

Methods: We generated over 100,000 full-field Cell Painting images of human alveolar adenocarcinoma basal epithelial cells (A549s) and human pulmonary microvascular endothelial cells (HPMECs) under different hypoxic conditions (1%~5% of oxygen content). These images were then submitted to our newly developed segmentation network (SegNet), which exhibited superior performance than traditional methods, to proceed to subcellular structure detection and segmentation. Subsequently, we created a hypoxia scoring network (HypoNet) using over 200,000 images of subcellular structures from A549s and HPMECs, demonstrating outstanding capacity in identifying cellular hypoxia status.

Results: We proposed a deep neural network-based drug screening pipeline (CPHNet), which facilitated the identification of two promising natural products, ferulic acid (FA) and resveratrol (RES). Both compounds demonstrated satisfactory anti-HAPE effects in a 3D-alveolus chip model (ex vivo) and a mouse model (in vivo).

Conclusion: This work provides a brand-new and effective pipeline for screening anti-HAPE agents by integrating artificial intelligence (AI) tools and Cell Painting, offering a novel perspective for AI-driven phenotypic drug discovery.

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CPHNet:通过基于深度学习的细胞绘画评分进行抗hape药物筛选的新管道。
背景:高原肺水肿(HAPE)对快速上升到高海拔地区的个体提出了重大的医学挑战。缺氧引起的肺泡-毛细血管屏障的细胞形态学改变,如线粒体结构改变和细胞骨架重组,在HAPE的发病机制中起着至关重要的作用。这些形态学变化对于理解细胞对缺氧的反应至关重要,并代表了潜在的治疗靶点。然而,目前仍缺乏基于这些细胞形态特征的抗hape治疗的有效药物发现策略。本研究旨在开发一个专注于细胞绘画图像形态学改变的管道,以确定HAPE干预的潜在治疗剂。方法:对不同缺氧条件(含氧量1%~5%)下的人肺泡腺癌基底上皮细胞(A549s)和人肺微血管内皮细胞(hpmes)进行了10万余张全视野细胞彩绘。然后将这些图像提交到我们新开发的分割网络(SegNet)中,该网络比传统方法具有更好的性能,进行亚细胞结构检测和分割。随后,我们利用A549s和hpmec的20多万张亚细胞结构图像创建了一个缺氧评分网络(HypoNet),显示出识别细胞缺氧状态的出色能力。结果:我们建立了基于深度神经网络的药物筛选管道(CPHNet),促进了阿魏酸(FA)和白藜芦醇(RES)两种有前景的天然产物的鉴定。这两种化合物在3d肺泡芯片模型(离体)和小鼠模型(体内)中均表现出令人满意的抗hape效果。结论:本研究结合人工智能(AI)工具和细胞绘画技术,为抗hape药物的筛选提供了全新有效的途径,为人工智能驱动的表型药物发现提供了新的视角。
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麦克林
tetramethylpyrazine
麦克林
tetramethylpyrazine
阿拉丁
acetazolamide
来源期刊
Respiratory Research
Respiratory Research RESPIRATORY SYSTEM-
CiteScore
9.70
自引率
1.70%
发文量
314
审稿时长
4-8 weeks
期刊介绍: Respiratory Research publishes high-quality clinical and basic research, review and commentary articles on all aspects of respiratory medicine and related diseases. As the leading fully open access journal in the field, Respiratory Research provides an essential resource for pulmonologists, allergists, immunologists and other physicians, researchers, healthcare workers and medical students with worldwide dissemination of articles resulting in high visibility and generating international discussion. Topics of specific interest include asthma, chronic obstructive pulmonary disease, cystic fibrosis, genetics, infectious diseases, interstitial lung diseases, lung development, lung tumors, occupational and environmental factors, pulmonary circulation, pulmonary pharmacology and therapeutics, respiratory immunology, respiratory physiology, and sleep-related respiratory problems.
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