Ontology highlight
ABSTRACT: Introduction
Fibrosis can damage the normal function of many organs, such as cardiac function, for which no effective clinical therapies exist. However, traditional approaches to anti-fibrosis drug discovery have primarily focused on the final biological indicators, often overlooking the dynamic morphological changes during fibrosis progression. Here, we present a novel approach, deep-DPC, which integrates label-free, time-series digital phase contrast (DPC) imaging with cell morphology analysis and unsupervised machine learning to dynamically control and monitor cell morphology.Objectives
This method enables discrimination between resting and activated fibrocytes and facilitates the discovery of non-invasive labeled anti-fibrotic lead compounds.Methods
The deep-DPC
SUBMITTER: Xing XD
PROVIDER: S-EPMC12685513 | biostudies-literature | 2025 Dec
REPOSITORIES: biostudies-literature