Computational mechanics simulations on epithelial folding (Strengths, insights, and future challenges)

• Material Type: 記事
• Title: Computational mechanics simulations on epithelial folding (Strengths, insights, and future challenges)
• Author Heading: MORIKAWA Kentaro; INOUE Yasuhiro
• Publication Date: 2024
• Publication Date (W3CDTF): 2024
• Periodical title: Journal of Biomechanical Science and Engineering
• No. or year of volume/issue: 19 2
• Volume: 19
• Issue: 2
• Pages: 23-00562-23-00562
• Publication date of volume/issue (W3CDTF): 2024
• ISSN (Periodical Title): 18809863
• Publication (Periodical Title): The Japan Society of Mechanical Engineers
• Text Language Code: en
• Subject Heading: Simulation; Epithelial folding; Apical constriction; Energy landscape; Mechanical interaction; Pattern formation; Differential growth
• Target Audience: 一般
• DOI: 10.1299/jbse.23-00562
• Access Restrictions: インターネット公開
• Related Material (URI): http://hdl.handle.net/2433/292062; https://www.jstage.jst.go.jp/article/jbse/19/2/19_23-00562/_pdf
• References: Left–right asymmetric cell intercalation drives directional collective cell movement in epithelial morphogenesis; https://cir.nii.ac.jp/crid/1050001339020462976; An energy landscape approach to understanding variety and robustness in tissue morphogenesis; https://cir.nii.ac.jp/crid/1050285700355938816; Impact of environmental asymmetry on epithelial morphogenesis; https://cir.nii.ac.jp/crid/1050577663293240064; Elasticity-based boosting of neuroepithelial nucleokinesis via indirect energy transfer from mother to daughter; https://cir.nii.ac.jp/crid/1050845763137914496; PCP-dependent transcellular regulation of actomyosin oscillation facilitates convergent extension of vertebrate tissue; https://cir.nii.ac.jp/crid/1360004232557330304; Reconstructing 3D deformation dynamics for curved epithelial sheet morphogenesis from positional data of sparsely-labeled cells; https://cir.nii.ac.jp/crid/1360004233464961664; Mechanical role of the spatial patterns of contractile cells in invagination of growing epithelial tissue; https://cir.nii.ac.jp/crid/1360004235502832000; Epithelial tissue folding pattern in confined geometry; https://cir.nii.ac.jp/crid/1360005515917836928; TAG-1–assisted progenitor elongation streamlines nuclear migration to optimize subapical crowding; https://cir.nii.ac.jp/crid/1360283691786861440; Structure and development of the complex helmet of treehoppers (Insecta: Hemiptera: Membracidae); https://cir.nii.ac.jp/crid/1360286996889219584; Instabilities of Monolayered Epithelia: Shape and Structure of Villi and Crypts; https://cir.nii.ac.jp/crid/1360292620982079488; Self-organizing optic-cup morphogenesis in three-dimensional culture; https://cir.nii.ac.jp/crid/1360564064158125312; Mechanical Regulation of Three-Dimensional Epithelial Fold Pattern Formation in the Mouse Oviduct; https://cir.nii.ac.jp/crid/1360567181974749696; Complex furrows in a 2D epithelial sheet code the 3D structure of a beetle horn; https://cir.nii.ac.jp/crid/1360567183435272320; Apical constriction: themes and variations on a cellular mechanism driving morphogenesis; https://cir.nii.ac.jp/crid/1360574095261943936; Unveiling the role of differential growth in 3D morphogenesis: An inference method to analyze area expansion rate distribution in biological systems; https://cir.nii.ac.jp/crid/1360581633344946048; Mechanical roles of apical constriction, cell elongation, and cell migration during neural tube formation in Xenopus; https://cir.nii.ac.jp/crid/1360848656234793856; Apical constriction: A cell shape change that can drive morphogenesis; https://cir.nii.ac.jp/crid/1360855568767582336; Villification: How the Gut Gets Its Villi; https://cir.nii.ac.jp/crid/1360855570116558464; Apoptotic Force and Tissue Dynamics During <i>Drosophila</i> Embryogenesis; https://cir.nii.ac.jp/crid/1361137044703931136; RhoA regulates initiation of invagination, but not convergent extension, during sea urchin gastrulation; https://cir.nii.ac.jp/crid/1361981468896997504; Differential proliferation rates generate patterns of mechanical tension that orient tissue growth; https://cir.nii.ac.jp/crid/1362544419792023552; Villification in the mouse: Bmp signals control intestinal villus patterning; https://cir.nii.ac.jp/crid/1362544419915036672; A wave of EGFR signaling determines cell alignment and intercalation in the<i>Drosophila</i>tracheal placode; https://cir.nii.ac.jp/crid/1363388846104828416; Mechanics of invagination and folding: Hybridized instabilities when one soft tissue grows on another; https://cir.nii.ac.jp/crid/1363670318989579904; Planar polarization of the atypical myosin Dachs orients cell divisions in <i>Drosophila</i>; https://cir.nii.ac.jp/crid/1363951793307451776; Compartmentalisation of Rho regulators directs cell invagination during tissue morphogenesis; https://cir.nii.ac.jp/crid/1364233268356411520
• Data Provider (Database): 国立情報学研究所 : CiNii Research; https://cir.nii.ac.jp/
• Original Data Provider (Database): Japan Link Center; https://japanlinkcenter.org/top; 学術機関リポジトリデータベース; https://irdb.nii.ac.jp; Crossref; https://www.crossref.org; 科学研究費助成事業データベース; https://kaken.nii.ac.jp/ja

• Summary, etc.: <p>Epithelial folding is a fundamental process governing the transformation of flat epithelial sheets into intricate three-dimensional structures duri...