Intermediate Domain-guided Adaptation for Unsupervised Chorioallantoic Membrane Vessel Segmentation

The chorioallantoic membrane (CAM) model is widely employed in angiogenesis research, and distribution of growing blood vessels is the key evaluation indicator. As a result, vessel segmentation is crucial for quantitative assessment based on topology and morphology. However, manual segmentation is extremely time-consuming, labor-intensive, and prone to inconsistency due to its subjective nature. Moreover, research on CAM vessel segmentation algorithms remains limited, and the lack of public datasets contributes to poor prediction performance. To address these challenges, we propose an innovative Intermediate Domain-guided Adaptation (IDA) method, which utilizes the similarity between CAM images and retinal images, along with existing public retinal datasets, to perform unsupervised training on CAM images. Specifically, we introduce a Multi-Resolution Asymmetric Translation (MRAT) strategy to generate intermediate images to promote image-level interaction. Then, an Intermediate Domain-guided Contrastive Learning (IDCL) module is developed to disentangle cross-domain feature representations. This method overcomes the limitations of existing unsupervised domain adaptation (UDA) approaches, which primarily concentrate on directly source-target alignment while neglecting intermediate domain information. Notably, we create the first CAM dataset to validate the proposed algorithm. Extensive experiments on this dataset show that our method outperforms compared approaches. Moreover, it achieves superior performance in UDA tasks across retinal datasets, highlighting its strong generalization capability. The CAM dataset and source codes are available at https://github.com/Light-47/IDA.

Label-free Prediction of Vascular Connectivity in Perfused Microvascular Networks in vitro

Continuous monitoring and in-situ assessment of microvascular connectivity have significant implications for culturing vascularized organoids and optimizing the therapeutic strategies. However, commonly used methods for vascular connectivity assessment heavily rely on fluorescent labels that may either raise biocompatibility concerns or interrupt the normal cell growth process. To address this issue, a Vessel Connectivity Network (VC-Net) was developed for label-free assessment of vascular connectivity. To validate the VC-Net, microvascular networks (MVNs) were cultured in vitro and their microscopic images were acquired at different culturing conditions as a training dataset. The VC-Net employs a Vessel Queue Contrastive Learning (VQCL) method and a class imbalance algorithm to address the issues of limited sample size, indistinctive class features and imbalanced class distribution in the dataset. The VC-Net successfully evaluated the vascular connectivity with no significant deviation from that by fluorescence imaging. In addition, the proposed VC-Net successfully differentiated the connectivity characteristics between normal and tumor-related MVNs. In comparison with those cultured in the regular microenvironment, the averaged connectivity of MVNs cultured in the tumor-related microenvironment decreased by 30.8%, whereas the non-connected area increased by 37.3%. This study provides a new avenue for label-free and continuous assessment of organoid or tumor vascularization in vitro.