{"title":"生长细胞聚集体中的图形多面体分裂","authors":"Urban Železnik, Matej Krajnc, Tanmoy Sarkar","doi":"arxiv-2408.07551","DOIUrl":null,"url":null,"abstract":"In the recently proposed Graph Vertex Model (GVM), cellular rearrangements\nare implemented as local graph transformations of the cell aggregate,\nrepresented by a knowledge graph [1]. This study extends GVM to incorporate\ncell division, a critical biological process involved in morphogenesis,\nhomeostasis, and disease progression. Like cellular rearrangements, cell\ndivision in GVM begins by identifying a subgraph of nodes and links, involved\nin the division, by matching suitable graph patterns or templates within the\nfull knowledge graph. The matched subgraph is then transformed to incorporate\ntopological changes within the knowledge graph, caused by the division event.\nImportantly, when this transformation is applied to a polygon in a 2D tiling,\nit performs the transformation, required to divide a polygon, indicating that\nthe 3D graph transformation is general and applicable also to 2D vertex models.\nOur extension of GVM enables the study of the dynamics of growing cell\naggregates in 3D to offer new insights into developmental processes and cancer\ngrowth.","PeriodicalId":501321,"journal":{"name":"arXiv - QuanBio - Cell Behavior","volume":"55 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Graph polyhedral divisions in growing cell aggregates\",\"authors\":\"Urban Železnik, Matej Krajnc, Tanmoy Sarkar\",\"doi\":\"arxiv-2408.07551\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In the recently proposed Graph Vertex Model (GVM), cellular rearrangements\\nare implemented as local graph transformations of the cell aggregate,\\nrepresented by a knowledge graph [1]. This study extends GVM to incorporate\\ncell division, a critical biological process involved in morphogenesis,\\nhomeostasis, and disease progression. Like cellular rearrangements, cell\\ndivision in GVM begins by identifying a subgraph of nodes and links, involved\\nin the division, by matching suitable graph patterns or templates within the\\nfull knowledge graph. The matched subgraph is then transformed to incorporate\\ntopological changes within the knowledge graph, caused by the division event.\\nImportantly, when this transformation is applied to a polygon in a 2D tiling,\\nit performs the transformation, required to divide a polygon, indicating that\\nthe 3D graph transformation is general and applicable also to 2D vertex models.\\nOur extension of GVM enables the study of the dynamics of growing cell\\naggregates in 3D to offer new insights into developmental processes and cancer\\ngrowth.\",\"PeriodicalId\":501321,\"journal\":{\"name\":\"arXiv - QuanBio - Cell Behavior\",\"volume\":\"55 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-08-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"arXiv - QuanBio - Cell Behavior\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/arxiv-2408.07551\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Cell Behavior","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2408.07551","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Graph polyhedral divisions in growing cell aggregates
In the recently proposed Graph Vertex Model (GVM), cellular rearrangements
are implemented as local graph transformations of the cell aggregate,
represented by a knowledge graph [1]. This study extends GVM to incorporate
cell division, a critical biological process involved in morphogenesis,
homeostasis, and disease progression. Like cellular rearrangements, cell
division in GVM begins by identifying a subgraph of nodes and links, involved
in the division, by matching suitable graph patterns or templates within the
full knowledge graph. The matched subgraph is then transformed to incorporate
topological changes within the knowledge graph, caused by the division event.
Importantly, when this transformation is applied to a polygon in a 2D tiling,
it performs the transformation, required to divide a polygon, indicating that
the 3D graph transformation is general and applicable also to 2D vertex models.
Our extension of GVM enables the study of the dynamics of growing cell
aggregates in 3D to offer new insights into developmental processes and cancer
growth.