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Cell-TIMP: Cellular Trajectory Inference based on Morphological Parameter
Department of Mechanical Engineering, Johns Hopkins University, Baltimore, Maryland, USA.
Örebro University, School of Science and Technology. (Centre for Applied Autonomous Sensor Systems (AASS))ORCID iD: 0000-0001-9364-7994
Department of Mechanical Engineering, Johns Hopkins University, Baltimore, Maryland, USA.
Department of Mechanical Engineering, Johns Hopkins University, Baltimore, Maryland, USA; The Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University, School of Medicine, Baltimore, Maryland, USA; Department of Oncology, Johns Hopkins University, Baltimore, Maryland, USA.
2024 (English)Manuscript (preprint) (Other academic)
Abstract [en]

Cellular morphology, shaped by various genetic and environmental influences, is pivotal to studying experimental cell biology, necessitating precise measurement and analysis techniques. Traditional approaches, which rely on geometric metrics derived from stained images, encounter obstacles stemming from both the imaging and analytical domains. Staining processes can disrupt the cell's natural state and diminish accuracy due to photobleaching, while conventional analysis techniques, which categorize cells based on shape to discern pathophysiological conditions, often fail to capture the continuous and asynchronous nature of biological processes such as cell differentiation, immune responses, and cancer progression. In this work, we propose the use of quantitative phase imaging for morphological assessment due to its label-free nature. For analysis, we repurposed the genomic analysis toolbox to perform trajectory inference analysis purely based on morphology information. We applied the developed framework to study the progression of leukemia and breast cancer metastasis. Our approach revealed a clear pattern of morphological evolution tied to the diseases' advancement, highlighting the efficacy of our method in identifying functionally significant shape changes where conventional techniques falter. This advancement offers a fresh perspective on analyzing cellular morphology and holds significant potential for the broader research community, enabling a deeper understanding of complex biological dynamics.

Place, publisher, year, edition, pages
2024. article id 2024.04.18.590109
National Category
Cell Biology
Identifiers
URN: urn:nbn:se:oru:diva-113679DOI: 10.1101/2024.04.18.590109PubMedID: 38712120OAI: oai:DiVA.org:oru-113679DiVA, id: diva2:1859990
Note

bioRxiv: 18.590109. Version 1.

PMID:  38712120

Available from: 2024-05-23 Created: 2024-05-23 Last updated: 2025-09-15Bibliographically approved

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Gupta, Himanshu

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