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| Autori principali: | , , , , , , , , , , , , , , , |
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| Natura: | Preprint |
| Pubblicazione: |
2025
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| Accesso online: | https://arxiv.org/abs/2512.14472 |
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| _version_ | 1866912768576192512 |
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| author | Li, Zelin Guan, Guoye Xian, Xiu Xie, Dongying Ma, Yiming You, Sicheng Zhu, Zhen Lee, Darrick Zhang, Zirui Ran, Zhuohen Wang, Chenwei Cao, Jianfeng Tang, Chao Huang, Zhaoke Zhao, Zhongying Yan, Hong |
| author_facet | Li, Zelin Guan, Guoye Xian, Xiu Xie, Dongying Ma, Yiming You, Sicheng Zhu, Zhen Lee, Darrick Zhang, Zirui Ran, Zhuohen Wang, Chenwei Cao, Jianfeng Tang, Chao Huang, Zhaoke Zhao, Zhongying Yan, Hong |
| contents | Deep learning segmentation and fluorescence imaging techniques allow the cellular morphology of living embryos to be constructed spatiotemporally. These development processes involve numerous molecules distributed at the subcellular scale, such as cell adhesion (E-cadherin), which accumulate at cell-cell interfaces to regulate intercellular connection. However, quantifying molecular distributions within specific subcellular regions across the entire embryo, where cell movement and molecular redistribution occur rapidly, is challenging due to the need for simultaneous cell morphology reconstruction and lineage tracing due to photobleaching and phototoxicity. We report a transformer-based pipeline, CTransformer, that establishes a 4D cellular morphology map before the 550-cell (late) stage. CTransformer constructed 4D cellular morphology atlases, reaching 80% accuracy at the 550-cell stage. Through this advanced architecture, we use only one channel to reconstruct cell morphology and achieve cell tracing. With each cell's morphology as a reference, the distribution of specific molecules throughout the cell body and at cell interfaces can be quantitatively measured in another fluorescence channel. We apply this methodology to track E-cadherin during embryonic development of the worm Caenorhabditis elegans, from fertilization to gastrulation. Our results reveal that E-cadherin is tightly regulated across individual embryos, both within single cells and at cell-cell interfaces, displaying an anterior-posterior gradient and cell- and lineage-specific patterns. Furthermore, its spatiotemporal heterogeneity influences cell mechanics and embryonic morphogenesis, helping explain how C. elegans achieves stereotypical developmental patterns at cellular resolution. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2512_14472 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | CTransformer: Deep-transformer-based 3D cell membrane tracking with subcellular-resolved molecular quantification Li, Zelin Guan, Guoye Xian, Xiu Xie, Dongying Ma, Yiming You, Sicheng Zhu, Zhen Lee, Darrick Zhang, Zirui Ran, Zhuohen Wang, Chenwei Cao, Jianfeng Tang, Chao Huang, Zhaoke Zhao, Zhongying Yan, Hong Biological Physics Deep learning segmentation and fluorescence imaging techniques allow the cellular morphology of living embryos to be constructed spatiotemporally. These development processes involve numerous molecules distributed at the subcellular scale, such as cell adhesion (E-cadherin), which accumulate at cell-cell interfaces to regulate intercellular connection. However, quantifying molecular distributions within specific subcellular regions across the entire embryo, where cell movement and molecular redistribution occur rapidly, is challenging due to the need for simultaneous cell morphology reconstruction and lineage tracing due to photobleaching and phototoxicity. We report a transformer-based pipeline, CTransformer, that establishes a 4D cellular morphology map before the 550-cell (late) stage. CTransformer constructed 4D cellular morphology atlases, reaching 80% accuracy at the 550-cell stage. Through this advanced architecture, we use only one channel to reconstruct cell morphology and achieve cell tracing. With each cell's morphology as a reference, the distribution of specific molecules throughout the cell body and at cell interfaces can be quantitatively measured in another fluorescence channel. We apply this methodology to track E-cadherin during embryonic development of the worm Caenorhabditis elegans, from fertilization to gastrulation. Our results reveal that E-cadherin is tightly regulated across individual embryos, both within single cells and at cell-cell interfaces, displaying an anterior-posterior gradient and cell- and lineage-specific patterns. Furthermore, its spatiotemporal heterogeneity influences cell mechanics and embryonic morphogenesis, helping explain how C. elegans achieves stereotypical developmental patterns at cellular resolution. |
| title | CTransformer: Deep-transformer-based 3D cell membrane tracking with subcellular-resolved molecular quantification |
| topic | Biological Physics |
| url | https://arxiv.org/abs/2512.14472 |