Publication: ACME: Automatic feature extraction for cell migration examination through intravital microscopy imaging.
| dc.contributor.author | Molina-Moreno, Miguel | |
| dc.contributor.author | González-Díaz, Iván | |
| dc.contributor.author | Sicilia, Jon | |
| dc.contributor.author | Crainiciuc, Georgiana | |
| dc.contributor.author | Palomino-Segura, Miguel | |
| dc.contributor.author | Hidalgo, Andres | |
| dc.contributor.author | Díaz-de-María, Fernando | |
| dc.contributor.funder | Ministerio de Economía y Competitividad (España) | es_ES |
| dc.contributor.funder | Comunidad de Madrid (España) | es_ES |
| dc.contributor.funder | Carlos III University of Madrid (España) | es_ES |
| dc.contributor.funder | Ministerio de Ciencia e Innovación (España) | es_ES |
| dc.contributor.funder | Fundación La Caixa | es_ES |
| dc.contributor.funder | Ministerio de Educación, Cultura y Deporte (España) | es_ES |
| dc.date.accessioned | 2023-04-03T11:24:19Z | |
| dc.date.available | 2023-04-03T11:24:19Z | |
| dc.date.issued | 2022-04 | |
| dc.description.abstract | Cell detection and tracking applied to in vivo fluorescence microscopy has become an essential tool in biomedicine to characterize 4D (3D space plus time) biological processes at the cellular level. Traditional approaches to cell motion analysis by microscopy imaging, although based on automatic frameworks, still require manual supervision at some points of the system. Hence, when dealing with a large amount of data, the analysis becomes incredibly time-consuming and typically yields poor biological information. In this paper, we propose a fully-automated system for segmentation, tracking and feature extraction of migrating cells within blood vessels in 4D microscopy imaging. Our system consists of a robust 3D convolutional neural network (CNN) for joint blood vessel and cell segmentation, a 3D tracking module with collision handling, and a novel method for feature extraction, which takes into account the particular geometry in the cell-vessel arrangement. Experiments on a large 4D intravital microscopy dataset show that the proposed system achieves a significantly better performance than the state-of-the-art tools for cell segmentation and tracking. Furthermore, we have designed an analytical method of cell behaviors based on the automatically extracted features, which supports the hypotheses related to leukocyte migration posed by expert biologists. This is the first time that such a comprehensive automatic analysis of immune cell migration has been performed, where the total population under study reaches hundreds of neutrophils and thousands of time instances. | es_ES |
| dc.description.peerreviewed | Sí | es_ES |
| dc.description.sponsorship | This work has been partially supported by the National Grant TEC2017-84395-P of the Spanish Ministry of Economy and Competitiveness, Madrid Regional Government and Universidad Carlos III de Madrid through the project SHARON-CM-UC3M, RTI2018- 095497-B-I00 from Ministerio de Ciencia e Innovación (MICINN) and HR17_00527 from Fundación La Caixa to A.H. M.M-M. is supported by the Spanish Ministry of Education, Culture and Sports FPU Grant FPU18/02825. M.P-S. is supported by a Federation of European Biochemical Societies long-term fellowship. J.S. is supported by a fellowship (PRE2019-089130) from MICINN. | es_ES |
| dc.format.page | 102358 | es_ES |
| dc.format.volume | 77 | es_ES |
| dc.identifier.citation | Med Image Anal. 2022 Apr;77:102358 | es_ES |
| dc.identifier.doi | 10.1016/j.media.2022.102358 | es_ES |
| dc.identifier.e-issn | 1361-8423 | es_ES |
| dc.identifier.journal | Medical image analysis | es_ES |
| dc.identifier.pubmedID | 35066392 | es_ES |
| dc.identifier.uri | http://hdl.handle.net/20.500.12105/15731 | |
| dc.language.iso | eng | es_ES |
| dc.publisher | Elsevier | es_ES |
| dc.relation.projectFECYT | info:eu-repo/grantAgreement/ES/TEC2017-84395-P | es_ES |
| dc.relation.projectFECYT | info:eu-repo/grantAgreement/ES/SHARON-CM-UC3M | es_ES |
| dc.relation.projectFECYT | info:eu-repo/grantAgreement/ES/RTI2018-095497-B-I00 | es_ES |
| dc.relation.projectFECYT | info:eu-repo/grantAgreement/ES/HR17_00527 | es_ES |
| dc.relation.projectFECYT | info:eu-repo/grantAgreement/ES/FPU18/02825 | es_ES |
| dc.relation.projectFECYT | info:eu-repo/grantAgreement/ES/PRE2019-089130 | es_ES |
| dc.relation.publisherversion | 10.1016/j.media.2022.102358 | es_ES |
| dc.repisalud.institucion | CNIC | es_ES |
| dc.repisalud.orgCNIC | CNIC::Grupos de investigación::Imagen de la Inflamación Cardiovascular y la Respuesta Inmune | es_ES |
| dc.rights.accessRights | open access | es_ES |
| dc.rights.license | Attribution-NonCommercial-NoDerivatives 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
| dc.subject.mesh | Image Processing, Computer-Assisted | es_ES |
| dc.subject.mesh | Neural Networks, Computer | es_ES |
| dc.subject.mesh | Cell Movement | es_ES |
| dc.subject.mesh | Diagnostic Imaging | es_ES |
| dc.subject.mesh | Humans | es_ES |
| dc.subject.mesh | Intravital Microscopy | es_ES |
| dc.title | ACME: Automatic feature extraction for cell migration examination through intravital microscopy imaging. | es_ES |
| dc.type | journal article | es_ES |
| dc.type.hasVersion | VoR | es_ES |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | 18d7e8cb-2cd8-4c07-8da8-81d3503c749f | |
| relation.isAuthorOfPublication | acb8e30b-34b9-4718-b517-8d5962f70950 | |
| relation.isAuthorOfPublication.latestForDiscovery | 18d7e8cb-2cd8-4c07-8da8-81d3503c749f |
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