npj Imaging最新文献

筛选
英文 中文
Automated smartphone based cell analysis platform. 基于智能手机的自动细胞分析平台。
npj Imaging Pub Date : 2025-10-22 DOI: 10.1038/s44303-025-00093-z
Meryem Beyza Avci, Fatma Kurul, Mehmet Turkan, Arif E Cetin
{"title":"Automated smartphone based cell analysis platform.","authors":"Meryem Beyza Avci, Fatma Kurul, Mehmet Turkan, Arif E Cetin","doi":"10.1038/s44303-025-00093-z","DOIUrl":"https://doi.org/10.1038/s44303-025-00093-z","url":null,"abstract":"<p><p>Cell analysis technologies play a critical role in biomedical research, enabling precise evaluation of essential parameters such as cell viability, density, and confluency. In this article, we introduce Quantella, a smartphone-based platform designed to perform comprehensive cell analysis encompassing these key metrics. Addressing limitations of conventional systems, such as high cost, hardware complexity, and limited adaptability, Quantella integrates low-cost optics, a rinsable flow cell, bluetooth-enabled hardware control, and a cloud-connected mobile application. Its adaptive image-processing pipeline employs multi-exposure fusion, thresholding, and morphological filtering for accurate, morphology-independent segmentation without requiring deep learning or user-defined parameters. System validation studies across diverse cell types showed deviations under 5% from flow cytometry. With the capacity to analyze over 10,000 cells per test, Quantella delivers high-throughput, reproducible results. Its accessible, scalable design makes it a promising tool for biomedical research, diagnostics, and education, particularly in resource-limited settings.</p>","PeriodicalId":501709,"journal":{"name":"npj Imaging","volume":"3 1","pages":"53"},"PeriodicalIF":0.0,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145351104","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Confounder-aware foundation modeling for accurate phenotype profiling in cell imaging. 在细胞成像中精确表型分析的混杂意识基础建模。
npj Imaging Pub Date : 2025-10-22 DOI: 10.1038/s44303-025-00116-9
Giorgos Papanastasiou, Pedro P Sanchez, Argyrios Christodoulidis, Guang Yang, Walter Hugo Lopez Pinaya
{"title":"Confounder-aware foundation modeling for accurate phenotype profiling in cell imaging.","authors":"Giorgos Papanastasiou, Pedro P Sanchez, Argyrios Christodoulidis, Guang Yang, Walter Hugo Lopez Pinaya","doi":"10.1038/s44303-025-00116-9","DOIUrl":"https://doi.org/10.1038/s44303-025-00116-9","url":null,"abstract":"<p><p>Image-based profiling is rapidly transforming drug discovery, offering unprecedented insights into cellular responses. However, experimental variability hinders accurate identification of mechanisms of action (MoA) and compound targets. Existing methods commonly fail to generalize to novel compounds, limiting their utility in exploring uncharted chemical space. To address this, we present a confounder-aware foundation model integrating a causal mechanism within a latent diffusion model, enabling the generation of balanced synthetic datasets for robust biological effect estimation. Trained on over 13 million Cell Painting images and 107 thousand compounds, our model learns robust cellular phenotype representations, mitigating confounder impact. We achieve state-of-the-art MoA and target prediction for both seen (0.66 and 0.65 ROC-AUC) and unseen compounds (0.65 and 0.73 ROC-AUC), significantly surpassing real and batch-corrected data. This innovative framework advances drug discovery by delivering robust biological effect estimations for novel compounds, potentially accelerating hit expansion. Our model establishes a scalable and adaptable foundation for cell imaging, holding the potential to become a cornerstone in data-driven drug discovery.</p>","PeriodicalId":501709,"journal":{"name":"npj Imaging","volume":"3 1","pages":"52"},"PeriodicalIF":0.0,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145351084","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Author Correction: The chicken chorioallantoic membrane as a low-cost, high-throughput model for cancer imaging. 作者更正:鸡绒毛膜尿囊膜是一种低成本、高通量的癌症成像模型。
npj Imaging Pub Date : 2025-10-18 DOI: 10.1038/s44303-025-00118-7
Lydia M Smith, Hannah E Greenwood, Will E Tyrrell, Richard S Edwards, Vittorio de Santis, Friedrich Baark, George Firth, Muhammet Tanc, Samantha Y A Terry, Anne Herrmann, Richard Southworth, Timothy H Witney
{"title":"Author Correction: The chicken chorioallantoic membrane as a low-cost, high-throughput model for cancer imaging.","authors":"Lydia M Smith, Hannah E Greenwood, Will E Tyrrell, Richard S Edwards, Vittorio de Santis, Friedrich Baark, George Firth, Muhammet Tanc, Samantha Y A Terry, Anne Herrmann, Richard Southworth, Timothy H Witney","doi":"10.1038/s44303-025-00118-7","DOIUrl":"10.1038/s44303-025-00118-7","url":null,"abstract":"","PeriodicalId":501709,"journal":{"name":"npj Imaging","volume":"3 1","pages":"51"},"PeriodicalIF":0.0,"publicationDate":"2025-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12535587/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145318999","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Phosphatidylserine exposure and plasma membrane perforation as ferroptotic signatures for in vivo imaging. 磷脂酰丝氨酸暴露和质膜穿孔作为体内成像的铁下垂特征。
npj Imaging Pub Date : 2025-10-06 DOI: 10.1038/s44303-025-00110-1
Ali Yasin Sonay, Elana Apfelbaum, Benedict Edward Mc Larney, Jan Grimm
{"title":"Phosphatidylserine exposure and plasma membrane perforation as ferroptotic signatures for in vivo imaging.","authors":"Ali Yasin Sonay, Elana Apfelbaum, Benedict Edward Mc Larney, Jan Grimm","doi":"10.1038/s44303-025-00110-1","DOIUrl":"10.1038/s44303-025-00110-1","url":null,"abstract":"<p><p>Ferroptosis emerged as a cell death modality against cancer, but there are currently no available biomarkers for imaging ferroptosis-based therapies. To address this, we evaluated phosphatidylserine exposure and perforation of lipid membranes during ferroptosis to explore potential targeting opportunities. We demonstrated that nano-sized gaps at late stage ferroptosis can serve as entry points for dyes that can bind to intracellular structures. These changes were accompanied with cellular signaling components similar to platelet activation, with phosphatidylserine exposure on the cell surface as a potential target for imaging programed cell death, including ferroptosis. We employed a novel tumor-seeking dye CJ215 that can also label apoptotic cells and showed that CJ215 accumulates in ferroptotic cells both in vitro and in vivo by binding to phosphatidylserine, which can be prevented with ferroptosis inhibition. Since phosphatidylserine exposure also occurs during apoptosis, CJ215 can monitor both apoptosis and ferroptosis-based therapies.</p>","PeriodicalId":501709,"journal":{"name":"npj Imaging","volume":"3 1","pages":"48"},"PeriodicalIF":0.0,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12500960/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145240655","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Author Correction: Aldehydic load as an objective imaging biomarker of mild traumatic brain injury. 作者更正:醛负荷作为轻度创伤性脑损伤的客观成像生物标志物。
npj Imaging Pub Date : 2025-10-06 DOI: 10.1038/s44303-025-00114-x
Alexia Kirby, Cian Ward, Clara S Goulet, Nicholas D Calvert, Ryan Daniel, Joseph Wai-Hin Leung, Ashwin Sharma, Mojmír Suchý, Cassandra Donatelli, Jing Wang, Emily Standen, Adam J Shuhendler
{"title":"Author Correction: Aldehydic load as an objective imaging biomarker of mild traumatic brain injury.","authors":"Alexia Kirby, Cian Ward, Clara S Goulet, Nicholas D Calvert, Ryan Daniel, Joseph Wai-Hin Leung, Ashwin Sharma, Mojmír Suchý, Cassandra Donatelli, Jing Wang, Emily Standen, Adam J Shuhendler","doi":"10.1038/s44303-025-00114-x","DOIUrl":"10.1038/s44303-025-00114-x","url":null,"abstract":"","PeriodicalId":501709,"journal":{"name":"npj Imaging","volume":"3 1","pages":"47"},"PeriodicalIF":0.0,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12500943/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145240632","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enhanced maximum intensity projection (eMIP) for improving the fidelity of optoacoustic images. 用于提高光声图像保真度的增强最大强度投影(eMIP)。
npj Imaging Pub Date : 2025-10-06 DOI: 10.1038/s44303-025-00112-z
Manuel Gehmeyr, María Begoña Rojas López, Suhanyaa Nitkunanantharajah, Hubert Preißl, Andreas Vosseler, Reiner Jumpertz von Schwartzenberg, Andreas L Birkenfeld, Nikoletta Katsouli, Nikolina-Alexia Fasoula, Angelos Karlas, Michael Kallmayer, Anette-Gabriele Ziegler, Dominik Jüstel, Vasilis Ntziachristos
{"title":"Enhanced maximum intensity projection (eMIP) for improving the fidelity of optoacoustic images.","authors":"Manuel Gehmeyr, María Begoña Rojas López, Suhanyaa Nitkunanantharajah, Hubert Preißl, Andreas Vosseler, Reiner Jumpertz von Schwartzenberg, Andreas L Birkenfeld, Nikoletta Katsouli, Nikolina-Alexia Fasoula, Angelos Karlas, Michael Kallmayer, Anette-Gabriele Ziegler, Dominik Jüstel, Vasilis Ntziachristos","doi":"10.1038/s44303-025-00112-z","DOIUrl":"10.1038/s44303-025-00112-z","url":null,"abstract":"<p><p>Three-dimensional (3D) image reconstructions are often rendered as two-dimensional images, using maximum intensity projections (MIPs). However, MIP's rendering fidelity depends on the alignment of the individual slices along the projection direction. Also, the presence of noise and artifacts affects the contrast and the projected image elements. We introduce enhanced MIP (eMIP), a methodology that aligns the boundaries (e.g., skin boundary) of adjacent slices of the 3D volume onto the same coordinate system assumed by MIP (e.g., same depth) and applies robust contrast adjustment to normalize the intensities of the projected slices. We benchmark eMIP on 1725 clinical scans of human skin, using raster-scan optoacoustic mesoscopy (RSOM) that were assessed by 8 experts. Our results show that eMIP facilitates interpretability compared to conventional MIP and increases consistently the perceived image quality. The improved diagnostic ability of eMIP has the potential to replace MIP in RSOM and similar modalities.</p>","PeriodicalId":501709,"journal":{"name":"npj Imaging","volume":"3 1","pages":"49"},"PeriodicalIF":0.0,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12501383/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145240686","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Super-resolution imaging with nanopipettes. 纳米吸管的超分辨率成像。
npj Imaging Pub Date : 2025-09-22 DOI: 10.1038/s44303-025-00108-9
Steffan Møller Sønderskov, Lasse Hyldgaard Klausen, Sebastian Amland Skaanvik, Xiaojun Han, Mingdong Dong
{"title":"Super-resolution imaging with nanopipettes.","authors":"Steffan Møller Sønderskov, Lasse Hyldgaard Klausen, Sebastian Amland Skaanvik, Xiaojun Han, Mingdong Dong","doi":"10.1038/s44303-025-00108-9","DOIUrl":"10.1038/s44303-025-00108-9","url":null,"abstract":"<p><p>Uncovering structural information of biological systems at the nanoscale is vital for understanding their dynamics and function. Nanoscale imaging techniques that obtain structural information down to the single-molecule level under physiologically relevant conditions and without affecting the fragile structure of biomaterials are limited. Thus, the realization of such techniques is highly attractive, especially within the biological sciences. Nanopipette-based imaging using scanning ion conductance microscopy (SICM) fulfills these requirements, but resolution limitations and artefact formation hinder obtaining accurate structural information on the scale comparable to the pipette tip. Here, we present a novel technique, super-resolution SICM (SR-SICM), based on image deconvolution using simulated pipette point-spread functions. The technique is demonstrated on different types of nanostructures, where it surpasses the lateral resolution limit of SICM and mitigates imaging artefacts considerably. SR-SICM is applicable to any SICM dataset through user-friendly downloadable software promoting the possibility of single-molecule studies on a routine basis.</p>","PeriodicalId":501709,"journal":{"name":"npj Imaging","volume":"3 1","pages":"46"},"PeriodicalIF":0.0,"publicationDate":"2025-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12454638/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145126681","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Radiomics in preclinical imaging research: methods, challenges and opportunities. 放射组学在临床前影像学研究中的应用:方法、挑战和机遇。
npj Imaging Pub Date : 2025-09-22 DOI: 10.1038/s44303-025-00104-z
Vlora Riberdy, Alessandro Guida, James Rioux, Kimberly Brewer
{"title":"Radiomics in preclinical imaging research: methods, challenges and opportunities.","authors":"Vlora Riberdy, Alessandro Guida, James Rioux, Kimberly Brewer","doi":"10.1038/s44303-025-00104-z","DOIUrl":"10.1038/s44303-025-00104-z","url":null,"abstract":"<p><p>Radiomics-based analyses are increasingly being applied to clinical studies. Radiomic features can be correlated with markers of disease severity or treatment success to improve early detection of disease and develop predictive models for therapeutic response. While radiomics has similar potential in preclinical research, its use in this context entails unique challenges. This paper provides an overview of the current state of radiomics in preclinical imaging, methodologies, challenges and future prospects.</p>","PeriodicalId":501709,"journal":{"name":"npj Imaging","volume":"3 1","pages":"45"},"PeriodicalIF":0.0,"publicationDate":"2025-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12454655/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145126703","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enigmatic tubular ultrastructure in the bacterial defensive symbiont of the Asian citrus psyllid Diaphorina citri. 亚洲柑橘木虱细菌防御共生体的谜管状超微结构。
npj Imaging Pub Date : 2025-09-18 DOI: 10.1038/s44303-025-00107-w
Chihong Song, Junnosuke Maruyama, Kazuyoshi Murata, Toshinobu Suzaki, Atsushi Nakabachi
{"title":"Enigmatic tubular ultrastructure in the bacterial defensive symbiont of the Asian citrus psyllid Diaphorina citri.","authors":"Chihong Song, Junnosuke Maruyama, Kazuyoshi Murata, Toshinobu Suzaki, Atsushi Nakabachi","doi":"10.1038/s44303-025-00107-w","DOIUrl":"10.1038/s44303-025-00107-w","url":null,"abstract":"<p><p>Candidatus Profftella armatura (Betaproteobacteria) is an organelle-like defensive symbiont inhabiting the symbiotic organ of a devastating citrus pest, the Asian citrus psyllid Diaphorina citri. Previous two-dimensional electron microscopy hinted at unprecedented ultrastructures in Profftella, but their precise architecture and composition were unknown. Here, using serial block-face scanning electron microscopy, high-voltage electron tomography, and fluorescence in situ hybridization, we show that elongated Profftella cells (2.8-136 μm observed) contain multiple tubes (1-43 per cell) up to 45 μm long. These tubes, occupying ~6.3% of the cell volume, are composed of five or six fibers twisted into a right-handed helix with a consistent diameter of ~230 nm. Their stability under high vacuum suggests a mechanical support role in elongated Profftella. Close association with ribosomes implies a possible role in protein synthesis. Our findings provide insight into the structural adaptations of intracellular symbionts and may inform strategies for controlling citrus pests.</p>","PeriodicalId":501709,"journal":{"name":"npj Imaging","volume":"3 1","pages":"44"},"PeriodicalIF":0.0,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12446461/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145088738","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fungal infections in focus: accelerating non-invasive imaging from preclinical insights to clinical breakthroughs. 聚焦真菌感染:加速非侵入性成像从临床前洞察到临床突破。
npj Imaging Pub Date : 2025-09-16 DOI: 10.1038/s44303-025-00105-y
Lauren Michiels, Mahrukh Shameem, Eliane Vanhoffelen, Agustin Reséndiz-Sharpe, Simon A Johnston, Nicolas Beziere, Greetje Vande Velde
{"title":"Fungal infections in focus: accelerating non-invasive imaging from preclinical insights to clinical breakthroughs.","authors":"Lauren Michiels, Mahrukh Shameem, Eliane Vanhoffelen, Agustin Reséndiz-Sharpe, Simon A Johnston, Nicolas Beziere, Greetje Vande Velde","doi":"10.1038/s44303-025-00105-y","DOIUrl":"10.1038/s44303-025-00105-y","url":null,"abstract":"<p><p>Invasive fungal diseases (IFDs) present a growing clinical challenge, underscoring the urgent need for improved diagnostics, therapeutics and mechanistic understanding. This review highlights the key role of innovative imaging techniques across all scales - ranging from whole-body-level diagnostics and therapy monitoring to host-pathogen interactions at cellular resolution in both clinical and preclinical settings. These imaging modalities facilitate translation of preclinical innovations into clinical applications, accelerating research and advancing IFD management.</p>","PeriodicalId":501709,"journal":{"name":"npj Imaging","volume":"3 1","pages":"42"},"PeriodicalIF":0.0,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12441154/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145077051","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信